14 NP_705833 L856S not found in SNVbox database
2304 NP_705833 K246N not found in SNVbox database
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr16:7637262 C>T maps to NM_145891.2 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:9252102 G>A maps to NM_000014.4 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr12:9225049 C>T maps to NM_000014.4 K1336K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:12726406 G>A maps to NM_001013630.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:70287877 G>A maps to ENST00000418685 L830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr6:44278040 G>A maps to NM_020745.2 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr7:121733108 C>A maps to NM_005763.3 E587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EI-01A-11D-A33E-09 chr16:8857958 C>T maps to NM_001127448.1 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr9:107581063 G>T maps to NM_005502.3 S1114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr2:215831611 A>G maps to NM_173076.2 L1948L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr7:48314975 G>T maps to NM_152701.3 E1905*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr7:48414000 G>T maps to NM_152701.3 G3731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr7:48312580 C>T maps to NM_152701.3 H1106H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2F-01A-11D-A387-09 chr16:2329035 G>A maps to NM_001089.2 G1485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr1:94463414 G>T did not map to a codon.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr1:94497567 G>A maps to NM_000350.2 N1298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:94463578 G>A maps to NM_000350.2 F2189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:1048894 C>T maps to NM_019112.3 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:1062212 C>T maps to NM_019112.3 Y1871Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr17:66877335 T>C maps to NM_007168.2 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr17:66979868 G>A maps to NM_080283.3 Q1541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr7:87175277 G>A maps to NM_000927.3 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JK-01A-11D-A36J-09 chr7:87214968 A>G maps to NM_000927.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr7:87174309 T>G maps to NM_000927.3 A631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BN-01A-11D-A37C-09 chr1:229667401 C>T maps to NM_012089.2 E472E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr2:169826676 G>A maps to NM_003742.2 Q563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr7:20689757 G>A maps to NM_001163941.1 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr2:220074952 G>A maps to NM_005689.2 R807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr23:74293528 C>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:150741289 C>T maps to ENST00000297504 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr16:48234246 C>T maps to NM_032583.3 E674E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:48234210 G>A maps to NM_032583.3 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr16:48162474 C>T maps to NM_033226.2 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:48173106 C>T maps to NM_033226.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr16:48122489 C>T maps to NM_033226.2 G1147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr10:101595897 C>T maps to NM_000392.3 T1155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr17:48757260 G>A did not map to a codon.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr16:16244583 C>G maps to NM_001171.5 R1418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68J-01A-11D-A307-09 chr16:16248795 G>A maps to NM_001171.5 I1325I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:17429952 G>A maps to ENST00000302539 Q937*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:17483345 C>T maps to ENST00000302539 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr23:153008508 C>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:94939327 C>T maps to ENST00000454898 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr4:89034697 C>T maps to NM_004827.2 E317E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:89020482 G>A maps to NM_004827.2 F495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:119024742 G>A maps to NM_001142505.1 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr2:44102439 C>T maps to NM_022437.2 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr17:27889777 C>T maps to NM_198147.2 W403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr17:47295201 C>T maps to NM_016428.2 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr4:8079399 G>A maps to NM_001130083.1 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:136131316 C>T maps to NM_020469.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:136131469 G>A maps to NM_020469.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:150554580 C>T maps to ENST00000416793 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr8:107782100 C>T maps to NM_139166.4 K106K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr6:26598572 G>A maps to NM_013375.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:34180929 G>A maps to NM_145804.2 F870F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:109634871 T>C maps to NM_001093.3 I847I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr12:112167712 C>G maps to NM_001136538.1 L480L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:132337553 G>A maps to NM_032169.4 H446H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr15:89381936 G>A maps to NM_013227.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr4:156784865 T>C maps to NM_017419.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr4:156773429 A>G maps to NM_017419.2 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:44074617 G>A maps to NM_001031854.2 E316E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:6307228 C>T maps to NM_133492.2 W187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr19:6307290 T>A maps to NM_133492.2 K167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr17:40025732 G>C maps to ENST00000401700 T1059T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr9:32407427 G>A did not map to a codon.
Sequencing variant TCGA-IE-A3OV-01A-11D-A228-09 chr5:80626230 C>T maps to NM_130767.2 G550G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ER-01A-11D-A36J-09 chr3:58514610 A>C maps to NM_003500.3 Y355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr4:8396466 T>C maps to NM_003501.2 Q353Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:11687291 G>A maps to NM_001111036.1 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DN-01A-12D-A27P-09 chr23:70823835 G>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:6151749 C>T maps to NM_030924.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr17:48539877 C>T maps to ENST00000427954 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A8OO-01A-11D-A36J-09 chr23:108904871 G>A did not map to a codon.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr23:108887383 C>G did not map to a codon.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr5:131305833 G>A maps to NM_001009185.1 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:131309054 G>A maps to NM_001009185.1 F369F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:20554274 C>T maps to NM_182617.3 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr16:20442561 C>T maps to NM_017888.2 N409N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr20:33501957 C>T maps to NM_001076552.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:81536977 A>G maps to NM_024560.2 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr5:56778453 G>A maps to NM_001017992.2 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:56777817 C>G maps to NM_001017992.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr19:39214575 G>C did not map to a codon.
Sequencing variant TCGA-FX-A8OO-01A-11D-A36J-09 chr19:39195637 C>T maps to NM_004924.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr23:127185555 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2P-01A-11D-A387-09 chr16:84230348 C>T maps to NM_139174.3 A623A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr2:9630590 A>G maps to NM_003183.4 F730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr2:9675992 G>T maps to NM_003183.4 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr14:70924557 C>G maps to NM_003813.2 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:70926144 G>A maps to NM_003813.2 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr7:87774474 T>A maps to NM_021723.3 I452I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr8:24168920 C>T maps to NM_014265.4 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr8:24193161 G>A maps to NM_021777.3 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr4:175898451 A>G maps to NM_014269.4 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:3652609 G>A maps to NM_025220.2 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr8:24339812 T>C maps to ENST00000380789 V288V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UC-01A-11D-A307-09 chr10:72517794 C>T maps to NM_139155.2 C1008C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr11:130319822 C>T maps to NM_139055.2 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AK-01A-21D-A24N-09 chr15:100739617 G>T maps to NM_139057.2 Y362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr16:77334274 C>T maps to NM_199355.2 G853G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:77356354 G>A maps to NM_199355.2 R681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:128983561 C>T maps to NM_133638.3 I653I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr5:178585760 G>A maps to NM_014244.4 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:178541188 C>T maps to NM_014244.4 R1105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr12:43821217 C>A maps to ENST00000389420 E1334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr12:43925908 C>T maps to ENST00000389420 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr12:43826171 G>A maps to ENST00000389420 R1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr4:73280607 T>G maps to NM_014243.1 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:73205401 G>A maps to NM_014243.1 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:79058436 C>T maps to ENST00000258883 L1272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:18680327 G>A maps to NM_001040272.4 W385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr15:84611407 A>G maps to NM_207517.2 R726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:154562359 C>T maps to ENST00000292205 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:154569411 G>A maps to ENST00000292205 V756V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr10:1284347 G>A maps to NM_018702.2 Q403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:145616616 C>T maps to NM_174922.3 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:145616617 C>T maps to NM_174922.3 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr8:145616874 C>T maps to NM_174922.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr1:167863153 C>T maps to NM_018417.4 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr5:7820783 A>C maps to NM_020546.2 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:24795083 C>T maps to NM_139247.3 K555K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr14:24802125 C>T maps to NM_139247.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr16:50325792 C>T maps to NM_001114.3 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80J-01A-11D-A36J-09 chr8:132051898 G>A maps to NM_001115.2 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HZ-01A-11D-A38Z-09 chr7:31120237 C>T maps to ENST00000409489 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr7:31124407 C>G maps to ENST00000409489 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3NK-01A-11D-A21Q-09 chr4:2930210 G>A maps to NM_014189.2 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr4:100349112 G>T maps to NM_000673.4 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:100340162 C>T maps to NM_000673.4 W326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:202912940 G>A maps to NM_015999.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr18:77896691 A>G maps to NM_014913.3 *1132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr18:77896526 C>T maps to NM_014913.3 S1077S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr5:148206525 C>T maps to NM_000024.5 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr14:105207462 G>T maps to NM_199165.1 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr7:44152924 T>C maps to NM_001129.3 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr7:44153421 C>T maps to NM_001129.3 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr10:116093019 C>T maps to NM_001001936.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr23:148048589 A>G did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:147744249 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:147744269 C>T did not map to a codon.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr23:148037965 C>T did not map to a codon.
Sequencing variant TCGA-IS-A3K6-01A-11D-A21Q-09 chr23:148037567 G>T did not map to a codon.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr23:148038142 G>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:148035200 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr23:148062300 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:100209980 G>A maps to NM_001025108.1 N739N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:76201263 C>T maps to NM_001145526.1 N186N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr4:74303890 G>C maps to NM_001134.1 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:86791005 C>T maps to NM_152336.2 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr15:86822902 C>T maps to NM_152336.2 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr11:47726170 C>T maps to ENST00000357610 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:32150475 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr5:76358969 A>T maps to NM_018046.4 K680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:141351366 G>T maps to NM_018238.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr7:141315306 C>T maps to NM_018238.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr21:45401060 G>A maps to NM_001037553.1 V345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr2:178257537 A>G maps to NM_003659.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:88204542 C>T maps to ENST00000395847 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr23:115303839 T>A did not map to a codon.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr5:35033585 A>T maps to NM_031900.3 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A971-01A-11D-A387-09 chr4:109683975 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:105409322 G>A maps to NM_138420.2 S4155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr7:17369625 A>C maps to NM_001621.4 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr23:129290458 T>A did not map to a codon.
Sequencing variant TCGA-DX-A2IZ-01A-11D-A21Q-09 chr14:96875256 G>A maps to NM_152327.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr17:55189858 A>G maps to ENST00000427138 Q703Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr9:112900710 A>C maps to NM_007203.4 R963R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:49957155 G>A did not map to a codon.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr14:33015885 C>G maps to NM_004274.4 S676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr14:33014695 T>C maps to NM_004274.4 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:15508396 G>A maps to NM_014371.2 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr7:91641894 G>A maps to NM_005751.4 K1157K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr7:91694630 C>T maps to NM_005751.4 Q2022*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr6:109837057 A>C did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:109391373 C>T maps to NM_152763.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:137791356 G>T maps to NM_005989.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr1:19593930 G>A maps to NM_201252.3 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:52237961 C>T maps to ENST00000441729 Q188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K6-01A-11D-A21Q-09 chr23:55047608 C>A did not map to a codon.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr23:55051215 C>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:105425712 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:19209671 C>T maps to NM_003748.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:19200960 G>A maps to NM_003748.3 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A67I-01A-31D-A307-09 chr6:24502779 C>T maps to NM_170740.1 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:165649753 G>A maps to NM_000696.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr1:165649860 C>A maps to NM_000696.3 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr1:165638238 C>A maps to NM_000696.3 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:30079986 C>T maps to ENST00000395248 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr12:34179345 C>T maps to NM_032834.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr22:50297506 C>T maps to NM_024105.3 E482E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr22:50297505 T>G maps to NM_024105.3 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:111002985 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr3:125652481 C>A maps to NM_001195223.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J0-01A-11D-A21Q-09 chr9:101980656 A>T maps to NM_033087.3 Y270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:111711379 G>A maps to ENST00000428306 Q623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr2:29456562 C>G did not map to a codon.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr2:30143132 G>A maps to NM_004304.3 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr2:3750074 C>T maps to ENST00000403787 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:73681153 C>T maps to NM_015120.4 L2499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr10:45939224 C>A maps to NM_000698.2 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:85383922 C>T maps to NM_020778.4 T673T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr2:202488978 T>C maps to ENST00000409099 *414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr8:11189397 C>T maps to NM_054028.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:71472161 C>T maps to NM_016519.4 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:71472326 C>T maps to NM_016519.4 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr11:46456426 C>A maps to ENST00000458649 L931L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr16:56438953 C>G did not map to a codon.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr16:56439138 C>T maps to NM_001144.4 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr14:103394779 G>A maps to NM_030943.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr23:112022790 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr1:115215869 G>A maps to NM_000036.2 D736D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr7:2740234 G>A maps to NM_133463.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr9:140070252 G>A maps to NM_013366.3 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr12:121747543 C>T maps to NM_016237.4 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr14:77275609 C>T maps to NM_015305.3 W147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr20:853734 T>A maps to NM_015985.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr9:129870419 G>A maps to NM_012098.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr4:114203898 C>T maps to NM_001148.4 N650N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr4:114275647 G>A maps to NM_001148.4 E1958E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:61833090 G>A maps to NM_020987.2 S2516S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:61955931 G>A maps to NM_020987.2 Q620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3NJ-01A-11D-A21Q-09 chr10:61833768 C>G maps to NM_020987.2 L2290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:61834560 C>T maps to NM_020987.2 K2026K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:113270706 C>T maps to NM_178510.1 F672F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr12:133324459 G>T maps to NM_015114.1 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A971-01A-11D-A387-09 chr12:133313589 C>A maps to NM_015114.1 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr2:241420381 C>T maps to ENST00000401804 K1006K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr2:241420514 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr13:111532382 G>A maps to NM_017664.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr12:110474118 C>T maps to NM_033121.1 D521D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:67059200 C>T maps to NM_207354.2 F175F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M4-01A-11D-A21Q-09 chr4:74012984 C>A maps to NM_032217.3 E578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr9:69423557 C>T maps to NM_001098805.1 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr19:4216722 G>A maps to ENST00000262970 E612E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr1:145561424 G>A maps to NM_144698.3 Q371Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:97830044 C>T maps to NM_001164315.1 F485F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr17:48773461 G>A maps to NM_052855.3 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:173616057 G>A maps to ENST00000367712 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:173596260 G>A maps to ENST00000367712 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr20:10030396 G>T maps to NM_198798.1 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VE-01A-11D-A29N-09 chr4:125593641 T>A maps to NM_020337.2 K264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr6:35051240 C>T maps to NM_015245.2 I985I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr7:36458928 T>C maps to NM_018685.2 S570S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr12:5744345 G>A maps to ENST00000356134 G597G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr11:22242680 C>T maps to NM_213599.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr2:242146994 A>G maps to NM_001001891.3 E383E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr15:90348419 G>T maps to NM_001150.2 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr8:124696848 C>T did not map to a codon.
Sequencing variant TCGA-PC-A5DK-01A-11D-A27P-09 chr5:150488014 C>T did not map to a codon.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr17:41008500 G>A maps to NM_003734.2 L742L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23V-01A-11D-A29N-09 chr19:50303238 C>T maps to NM_014203.2 A429A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr19:50308788 C>A maps to NM_014203.2 C830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:183897987 C>T maps to ENST00000411763 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr15:83328313 A>C maps to NM_004644.3 *1083G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:83345377 G>A maps to NM_004644.3 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A3PN-01A-11D-A228-09 chr19:2117231 T>A maps to ENST00000355272 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr19:2129393 G>A maps to ENST00000355272 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr9:72071279 C>T maps to NM_001163.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr9:72056031 C>G did not map to a codon.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr15:29346407 C>T maps to NM_005503.3 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EI-01A-11D-A33E-09 chr5:112175083 G>T maps to NM_001127510.2 E1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:112178968 C>T maps to NM_001127510.2 R2560*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr19:1455426 C>T maps to NM_005883.2 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr1:159558149 G>C maps to NM_001639.3 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:159558494 C>T maps to NM_001639.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr23:55033726 C>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:43342405 T>C maps to NM_001142930.1 F89F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr11:116691843 G>A maps to NM_000482.3 Y310Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr11:116661094 G>A maps to NM_052968.4 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr2:21263892 T>C maps to NM_000384.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:21238124 C>T maps to NM_000384.2 E1172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:21233940 C>T maps to NM_000384.2 L1933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:21245743 G>A maps to NM_000384.2 I925I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr2:21247912 G>T maps to NM_000384.2 Y776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:39380211 G>A maps to ENST00000402182 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr22:39439094 G>A maps to NM_145298.5 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:56755346 G>A maps to NM_001638.2 R215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:36123191 C>T maps to NM_030642.1 S359S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr12:105591571 G>T maps to NM_018171.3 C341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr12:105597500 G>A maps to NM_018171.3 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr2:241622005 G>A maps to NM_001102467.1 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr2:241622023 G>A maps to NM_001102467.1 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr18:24436261 T>C maps to NM_001650.4 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr18:24436237 G>A maps to NM_001650.4 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr12:50367324 G>A maps to NM_001652.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:25232849 C>T maps to NM_001169.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr23:66765154 T>A did not map to a codon.
Sequencing variant TCGA-IE-A4EK-01A-11D-A24N-09 chr23:66765154 T>A did not map to a codon.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr23:66765160 A>T did not map to a codon.
Sequencing variant TCGA-KD-A5QU-01A-11D-A27P-09 chr23:66765151 T>A did not map to a codon.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr23:66765596 C>T did not map to a codon.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr23:66765228 G>C did not map to a codon.
Sequencing variant TCGA-DX-A8BV-01A-11D-A37C-09 chr11:72404504 G>A maps to NM_001040118.2 V1273V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr4:36212334 G>A maps to NM_015230.2 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr4:36212250 T>G maps to NM_015230.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr4:36148955 C>T maps to NM_015230.2 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr5:141059358 G>T maps to NM_022481.5 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr8:68113721 C>T maps to NM_006421.3 E1749E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr14:68117432 G>A maps to NM_001172.3 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr10:24909074 A>G maps to NM_020824.3 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:94643581 C>T maps to NM_004815.3 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr1:161018647 T>C maps to NM_001025598.1 K721K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:130215688 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:145773497 G>A maps to NM_025251.1 I324I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr12:57872883 G>T maps to ENST00000393797 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:18023601 C>T maps to NM_018125.3 S1189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I0-01A-11D-A38Z-09 chr11:120291477 C>T maps to NM_015313.2 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr17:8218892 G>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:3389731 C>T maps to NM_014448.3 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:3397099 G>A maps to NM_014448.3 V693V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr11:73021101 G>A maps to NM_014786.3 T473T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr2:131803759 T>C maps to NM_015320.2 *691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr23:135827387 C>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:135757222 G>A did not map to a codon.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr1:27088785 C>T maps to NM_006015.4 Q799*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EK-01A-11D-A24N-09 chr6:157521933 G>A maps to ENST00000367148 E1442E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr6:157256632 C>T maps to ENST00000367148 Q641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr6:157520040 G>A maps to ENST00000367148 P1410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr15:74883554 C>T maps to ENST00000395077 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr15:74883521 T>C maps to ENST00000395077 C304C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr15:74883952 C>A maps to ENST00000395077 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr23:100229169 G>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:64785862 C>T maps to NM_001667.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr17:41477525 A>G maps to NM_001661.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:28233360 C>T did not map to a codon.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr16:31476246 G>T maps to NM_024742.2 E635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr3:137991909 G>T maps to ENST00000469044 V527V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3B-01A-11D-A417-09 chr23:100808827 G>T did not map to a codon.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr23:100871411 G>A did not map to a codon.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr12:110888065 C>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:169487278 G>A maps to NM_032487.4 I10I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr3:169485725 T>G maps to NM_032487.4 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:35835270 C>T maps to ENST00000458225 Q755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:35732378 C>T maps to ENST00000458225 Q190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:35729274 G>A maps to ENST00000458225 E102E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K8-01A-11D-A21Q-09 chr11:74978735 C>A maps to NM_004041.3 E369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr9:140508121 G>A maps to NM_152285.2 R112R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:4891306 G>A maps to NM_001080523.1 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr19:4891141 G>T maps to NM_001080523.1 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr23:2827907 G>A did not map to a codon.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr23:2864081 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr23:2876418 T>C did not map to a codon.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr23:2853044 A>G did not map to a codon.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr5:94927273 C>T maps to NM_198150.2 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr11:3685361 G>T maps to NM_004314.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:104660348 G>T did not map to a codon.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr8:17942298 G>T maps to NM_004315.4 C4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr2:9496212 G>A maps to NM_003887.2 Q383Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr1:23763475 G>A maps to NM_017707.3 H468H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:5683862 C>T maps to NM_024701.3 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr6:101253757 T>A did not map to a codon.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr1:155429651 T>C maps to ENST00000368346 P1674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:155450338 G>A maps to ENST00000368346 F774F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr1:155448259 G>A maps to ENST00000368346 P1467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:1743282 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:62430151 G>A maps to NM_004318.3 L687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr8:62415935 G>A maps to NM_004318.3 R753R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr22:26839162 G>T maps to NM_020437.4 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr11:62156673 C>T maps to NM_025080.3 G187G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:133355184 C>T maps to NM_000050.4 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr9:133370323 G>A maps to NM_000050.4 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr3:130743805 A>G maps to ENST00000514044 C115C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VE-01A-11D-A29N-09 chr2:96803347 G>T maps to NM_001002036.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr1:177001820 G>A maps to ENST00000281881 H212H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:176918415 G>A maps to ENST00000281881 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:177001985 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:176913032 G>A maps to ENST00000281881 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr9:119976715 G>A maps to ENST00000313400 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:119737614 G>A maps to ENST00000313400 F587F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:119770452 G>A maps to ENST00000313400 I503I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr18:31324428 C>T maps to NM_030632.1 F1539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr7:117020089 G>T maps to NM_130768.2 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr2:24149445 G>T maps to NM_017552.1 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:1425757 C>T maps to NM_031921.4 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:1417599 C>T maps to NM_031921.4 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr1:1386074 C>T maps to NM_001039211.2 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80J-01A-11D-A36J-09 chr1:1387814 G>A did not map to a codon.
Sequencing variant TCGA-DX-A240-01A-32D-A27P-09 chr17:29220694 C>T maps to NM_024857.3 D1608D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HZ-01A-11D-A38Z-09 chr22:39917545 T>G maps to NM_182810.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr16:10527499 G>A maps to NM_024997.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C7-01A-11D-A36J-09 chr2:234173535 A>G did not map to a codon.
Sequencing variant TCGA-JV-A75J-01A-11D-A32I-09 chr14:96784116 G>A maps to NM_018036.5 G985G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71P-01A-12D-A33E-09 chr2:216197213 A>G maps to NM_004044.6 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr14:51094954 C>T maps to ENST00000358385 F442F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:108153444 G>A maps to NM_000051.3 E1195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:108159766 C>T maps to NM_000051.3 A1391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:7043433 C>T maps to NM_001940.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr15:25924868 C>T maps to NM_024490.3 V1373V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr15:25940131 G>A maps to NM_024490.3 I974I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr4:47537546 C>A maps to NM_020453.3 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr4:47563057 T>A maps to NM_020453.3 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr13:25259492 T>A maps to NM_001185085.1 Y70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:42482803 G>A maps to ENST00000441343 F528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:28912047 G>A maps to NM_173201.3 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr17:3839702 C>T maps to NM_174953.1 W794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr1:203680133 G>A maps to NM_001001396.1 R643R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:203677213 T>C maps to NM_001001396.1 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr10:7844281 C>A maps to NM_001001973.1 Y229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr2:176044903 G>T maps to NM_001689.4 I14I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr23:153663636 G>C did not map to a codon.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr23:153660770 G>T did not map to a codon.
Sequencing variant TCGA-DX-A240-01A-32D-A27P-09 chr7:138447176 C>T maps to NM_130840.2 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr7:138429925 A>G maps to NM_130840.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:77289140 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:77245338 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr18:55328439 G>A maps to NM_005603.4 I891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:154315646 G>A maps to NM_020452.3 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:1787146 G>A maps to NM_138813.2 L1036L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr20:50255955 G>A maps to NM_006045.1 Q532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HZ-01A-11D-A38Z-09 chr3:142277618 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:3542926 G>A maps to NM_139321.2 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr10:117059563 C>A maps to NM_207303.2 G812G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:117228697 G>A maps to NM_207303.2 G1171G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr10:117059680 A>G maps to NM_207303.2 E851E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HL-01A-11D-A387-09 chr23:76890193 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr23:76931771 G>C did not map to a codon.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr23:76890127 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr23:76938580 C>A did not map to a codon.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr23:76937962 G>A did not map to a codon.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr23:76875919 G>A did not map to a codon.
Sequencing variant TCGA-DX-A3UD-01A-11D-A307-09 chr23:76939417 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr23:76937410 C>A did not map to a codon.
Sequencing variant TCGA-DX-A8BN-01A-11D-A37C-09 chr23:76939576 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr23:76909586 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr23:76849183 T>A did not map to a codon.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr23:76874271 A>T did not map to a codon.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr23:76937677 C>A did not map to a codon.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr23:76939958 C>T did not map to a codon.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr23:76909658 G>A did not map to a codon.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr23:76855961 T>A did not map to a codon.
Sequencing variant TCGA-JV-A5VE-01A-11D-A29N-09 chr23:76814203 C>A did not map to a codon.
Sequencing variant TCGA-KD-A5QU-01A-11D-A27P-09 chr23:76912103 G>C did not map to a codon.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr23:76872171 T>A did not map to a codon.
Sequencing variant TCGA-PC-A5DN-01A-12D-A27P-09 chr23:76875865 C>G did not map to a codon.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr23:76938685 T>A did not map to a codon.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr23:76939696 C>A did not map to a codon.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr23:76888727 T>A did not map to a codon.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr23:13337120 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr7:105254569 T>C maps to NM_020725.1 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr1:110034209 G>T maps to NM_153340.4 L675L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr9:94058336 C>T maps to NM_001698.2 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:57746715 C>T maps to NM_001015878.1 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr7:70254923 G>T maps to NM_015570.2 E908*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:69755361 G>A maps to NM_001127232.1 G223G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr12:58200181 C>T maps to NM_006576.3 L544L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr12:58204271 C>G maps to NM_006576.3 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB36-01A-11D-A417-09 chr12:58207179 G>A maps to NM_006576.3 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:69261810 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:160803876 G>A maps to NM_033168.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N1-A6IA-01A-12D-A32I-09 chr19:17918637 C>A maps to NM_014256.3 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr17:80914629 G>A maps to NM_001009905.1 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J4-01A-32D-A21Q-09 chr12:58025113 G>A maps to NM_001478.3 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J4-01A-32D-A21Q-09 chr12:58025074 G>T maps to NM_001478.3 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J4-01A-32D-A21Q-09 chr12:58025098 G>T maps to NM_001478.3 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr8:143562625 C>T maps to NM_001702.2 R614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:32196592 G>A maps to NM_001703.2 P1396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr6:69943232 C>A maps to NM_001704.2 T844T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr6:69684655 A>T maps to NM_001704.2 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:69684676 G>A maps to NM_001704.2 E516E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:69665970 G>A maps to NM_001704.2 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr7:97984423 T>A maps to NM_018842.4 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A3OV-01A-11D-A228-09 chr16:1391867 G>C did not map to a codon.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr4:102791782 A>T maps to NM_017935.4 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr3:52438590 G>A maps to NM_004656.2 D376D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B7-01A-11D-A307-09 chr1:91180170 G>A maps to NM_020063.1 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:96715200 C>T maps to NM_021570.3 Q164Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr6:31605305 G>T maps to NM_080686.2 R2139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VF-01A-11D-A29N-09 chr6:31613260 G>A maps to ENST00000404765 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr7:72856561 G>T maps to NM_032408.3 A1472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr12:57011221 G>A maps to NM_013449.3 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2J-01A-11D-A387-09 chr12:56993004 T>G maps to NM_013449.3 A1772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:27114883 G>A maps to NM_003986.2 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr15:73022024 G>A maps to NM_033028.3 K237K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:107474464 G>A maps to NM_001142568.1 Q282Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr23:152981003 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9I0-01A-11D-A38Z-09 chr1:94037298 C>T maps to NM_003567.2 A634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr3:165547450 C>T maps to NM_000055.2 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr19:41916827 C>T maps to NM_000709.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:80878665 C>T maps to NM_183050.2 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:60687934 C>T maps to NM_022893.3 G704G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:50169130 C>T maps to NM_138639.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:50169103 C>T maps to NM_138639.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr17:6930823 C>T maps to NM_181844.3 C442C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N1-A6IA-01A-12D-A32I-09 chr1:147084928 C>T maps to NM_004326.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:118769681 G>A maps to NM_182557.2 I1314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr11:118771358 G>A maps to NM_182557.2 N1031N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr16:81323974 C>T maps to NM_017429.2 V479V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr23:129147216 G>A did not map to a codon.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr23:129147376 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:129148781 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:219526215 C>T maps to NM_004328.4 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr4:104006542 G>A maps to NM_020139.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:70810862 G>A maps to NM_018429.2 R1521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr23:18189139 A>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:107391311 C>T maps to NM_001080450.2 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:42122233 C>T maps to NM_207406.3 K408K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr10:13541961 G>C maps to ENST00000396900 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:12867019 G>A maps to NM_017682.2 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr1:45250615 G>A maps to NM_153274.2 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr23:102564732 C>T did not map to a codon.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr22:18220803 G>A maps to NM_197966.1 Y231Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:127828347 G>A maps to NM_139343.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:22481520 G>A maps to NM_018688.4 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:32774387 C>T maps to NM_016252.3 A4328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:91292842 G>A maps to NM_000057.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr17:28601154 G>A maps to NM_000386.2 R236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr10:98031112 A>G maps to NM_013314.3 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr10:97951811 G>A maps to NM_013314.3 Q430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr10:97956690 G>A maps to NM_013314.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr19:40953795 C>G maps to NM_000713.2 *207Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr8:22064427 C>T maps to NM_006129.4 D765D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr8:22033794 C>T maps to NM_006129.4 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr2:69093563 G>A maps to NM_014482.1 Y158Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:50659391 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:43281058 C>T maps to NM_014753.3 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr15:83932019 C>T maps to NM_001717.3 G661G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:31604870 G>A maps to NM_025227.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr20:31622057 C>T maps to NM_174897.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr12:112110524 T>A maps to NM_006768.3 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr16:50357557 A>G maps to NM_001173984.2 D461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr16:50357502 C>A maps to NM_001173984.2 E480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr5:887532 G>A maps to NM_001009877.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr1:92470011 C>G maps to ENST00000347608 G822G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:55817696 C>T maps to NM_032430.1 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2F-01A-11D-A387-09 chr23:79989632 T>G did not map to a codon.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr23:80064058 G>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:49662557 C>T maps to NM_003458.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:49699681 G>A maps to NM_003458.3 R3468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:15716984 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr12:108051404 C>A maps to NM_001018072.1 T1075T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:108045474 C>T maps to NM_001018072.1 Q1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:3641301 C>A maps to NM_032444.2 V779V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DX-A7EU-01A-22D-A36J-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DX-AB2W-01A-11D-A38Z-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:92554329 C>G maps to NM_183242.3 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr23:100615556 C>G did not map to a codon.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr23:100611812 G>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:26509371 C>T maps to NM_001732.2 I517I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr6:26466201 G>A did not map to a codon.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr15:40505676 T>C did not map to a codon.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr17:56382429 C>A maps to NM_004758.2 E1846*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:56386602 C>A maps to NM_004758.2 E1344*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr10:63445875 A>T maps to NM_173554.2 K50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:124457605 G>A maps to NM_001010912.1 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BN-01A-11D-A37C-09 chr10:21805719 A>G maps to NM_207371.3 H344H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr10:21805482 C>T maps to NM_207371.3 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr10:73512759 C>A did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr10:32983810 T>C maps to ENST00000375025 H90H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr10:33165273 G>T did not map to a codon.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr10:50534396 G>A maps to NM_001135196.1 A1269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HL-01A-11D-A387-09 chr10:105944775 C>T maps to ENST00000389588 W714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr10:134755528 G>A maps to ENST00000368586 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K8-01A-11D-A21Q-09 chr11:76237558 T>C maps to ENST00000393457 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr11:111952738 T>C maps to NM_018195.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:108302544 G>A maps to NM_152587.3 H34H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:64717233 G>A maps to NM_001037225.1 F110F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr11:61541465 G>A maps to NM_001127392.1 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:91348285 T>C maps to NM_152638.2 Q78Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr12:82872801 G>C maps to NM_032230.2 *604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr12:82752385 C>G maps to NM_032230.2 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr12:52467506 C>T maps to NM_021934.4 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:52470781 C>T maps to NM_021934.4 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr12:105380150 C>G maps to NM_152318.2 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr12:112601462 C>T maps to NM_001109662.2 T4088T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:112630517 G>A maps to NM_001109662.2 G2874G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5Y8-01A-11D-A29N-09 chr12:97102549 C>T maps to ENST00000342887 N656N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V2-01A-11D-A32I-09 chr12:48577970 G>A maps to NM_001013635.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr14:90756882 C>T maps to NM_017970.2 V637V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr14:74823734 C>A maps to NM_018228.2 G83G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:74824865 G>A maps to NM_018228.2 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:76620780 G>A maps to NM_017926.2 W25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr14:50579350 G>T maps to NM_024558.2 Y219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:90263657 G>A maps to NM_145231.2 R141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr14:77319754 T>C did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:77292894 G>A maps to NM_194287.2 R19R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:77323730 G>A maps to NM_194287.2 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:77292846 C>T maps to NM_194287.2 I3I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ET-01A-11D-A36J-09 chr14:60945103 C>T maps to NM_174978.2 W79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr14:74186106 G>T maps to NM_001043318.1 S1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr14:103568581 C>T maps to NM_001077594.1 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr15:24921703 G>A maps to NM_018958.2 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr15:81440867 G>A maps to ENST00000458088 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr16:19584521 G>T maps to NM_020314.5 E212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr16:19659137 G>A maps to NM_020314.5 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr16:67174001 C>T maps to NM_025187.3 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr16:49412406 C>T maps to NM_144602.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr17:45517999 C>T maps to NM_152347.4 Q948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr17:57288308 G>A maps to NM_018149.6 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr17:7330143 G>A maps to NM_175734.4 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr18:13645199 C>T maps to NM_181481.3 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr19:30505903 G>A maps to NM_003796.2 L512L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr19:507659 C>T maps to NM_033513.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:3624117 T>A maps to NM_021231.1 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:16612274 C>T maps to NM_032207.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:16611857 C>T maps to NM_032207.2 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr19:7573141 A>G maps to NM_198534.2 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U7-01A-11D-A29N-09 chr19:14000050 G>A maps to ENST00000454313 Q540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr19:14000756 C>T maps to ENST00000454313 V304V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-KD-A5QU-01A-11D-A27P-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr12:7252336 G>C maps to NM_016546.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr1:111494596 A>T maps to NM_018372.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:172425562 G>A maps to NM_139240.3 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:200880853 C>T maps to NM_018265.2 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr1:200880697 G>A maps to NM_018265.2 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:36784741 C>T maps to NM_001162530.1 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:179354441 C>T maps to NM_144696.4 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:179399629 G>A maps to NM_144696.4 W459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr1:116675979 G>A maps to NM_152367.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr1:75037895 C>T maps to NM_001002912.4 S1166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:55152085 G>A maps to ENST00000454855 K921K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:55136210 C>T maps to ENST00000454855 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr1:43748629 G>T maps to NM_001164829.1 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr1:23695984 C>G maps to ENST00000507744 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:185143986 C>T maps to NM_001105518.1 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:154179926 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:228362717 C>T maps to NM_001010867.2 R223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:228362716 C>T maps to NM_001010867.2 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPF-01A-11D-A38Z-09 chr1:228362560 C>T maps to NM_001010867.2 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr1:153615715 C>T maps to NM_015607.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:43870166 G>A maps to ENST00000310739 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:60505852 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:60463383 G>A maps to NM_152377.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr1:60491104 G>A maps to NM_152377.2 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:34684343 G>A maps to NM_001134734.1 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:31877726 G>A maps to NM_033197.2 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr20:60987918 G>A maps to NM_080833.2 D571D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr20:60990632 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:34596372 C>T maps to ENST00000373973 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr20:31652608 G>T maps to NM_182658.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr20:31647705 T>G maps to NM_182658.1 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr20:31671210 G>T maps to NM_182519.2 G70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr20:20258029 C>T maps to ENST00000389655 D911D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:20322480 C>T maps to ENST00000389655 F1146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr20:24949548 C>T maps to NM_020531.2 W340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:257744 C>T maps to NM_153269.1 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr21:45953679 G>A maps to ENST00000443468 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr21:33651118 C>T maps to NM_018944.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr21:47588306 C>T maps to NM_001142854.1 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr21:30521519 C>T maps to NM_020152.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3NJ-01A-11D-A21Q-09 chr22:19839505 C>T maps to NM_024627.5 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr22:32550297 G>A maps to NM_001010859.1 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr22:32548572 C>T maps to NM_001010859.1 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr11:73814460 G>A maps to ENST00000334126 L765L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QU-01A-11D-A27P-09 chr2:27801964 A>C maps to NM_032266.3 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:20939874 G>A maps to ENST00000381090 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr2:24262325 C>G maps to NM_025203.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:24262259 G>A maps to NM_025203.2 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr2:11284203 G>A maps to NM_182500.2 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:74808945 G>A maps to NM_138804.3 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:29294163 G>A maps to NM_001029883.1 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:29295747 C>T maps to NM_001029883.1 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr2:120097418 G>A maps to NM_001017927.2 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:6693027 G>A maps to NM_000064.2 V1099V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr19:6712608 G>A maps to NM_000064.2 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr12:8211887 A>G maps to NM_004054.2 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:14756897 G>C maps to NM_032137.4 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr3:44437984 A>G maps to NM_173826.3 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr3:157318112 C>T maps to NM_001130001.1 Y115Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr3:69026828 A>G maps to ENST00000383701 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:207317959 T>C maps to NM_000715.3 D564D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HZ-01A-11D-A38Z-09 chr4:57843742 G>C maps to NM_032313.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:113509017 C>T maps to NM_018392.4 Q1065Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr4:113460789 G>A maps to NM_018392.4 L2076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:81791226 G>A maps to ENST00000508675 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:71020142 G>A maps to NM_214711.3 K17K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:93489825 C>T maps to ENST00000513200 W1238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr5:37239050 T>A maps to NM_023073.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:41149431 C>T maps to NM_001115131.1 W845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr5:41176763 C>T maps to NM_001115131.1 T327T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr6:35754851 G>T maps to NM_001010886.3 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr6:53986336 C>G maps to ENST00000502396 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:53989329 G>A maps to ENST00000502396 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr6:88120316 C>G maps to NM_001031743.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:121452830 G>A maps to ENST00000275159 N988N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:31691543 C>T maps to NM_138272.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:31735444 G>A maps to NM_025258.2 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr6:36882451 C>T maps to NM_152734.3 F233F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:151894523 C>T maps to ENST00000367290 I330I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2L-01A-32D-A417-09 chr5:40958328 G>A maps to NM_000587.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr7:25194753 G>A maps to NM_138811.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:39612145 C>T maps to NM_020192.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:92161863 G>A did not map to a codon.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr1:57378073 A>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:57406608 G>A maps to NM_000066.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr8:442473 G>A maps to NM_175075.3 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MO-A47R-01A-11D-A24N-09 chr8:124253559 G>C maps to NM_032847.1 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr8:27927796 G>A maps to ENST00000341513 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42W-01A-11D-A24N-09 chr5:39288846 G>A maps to NM_001737.3 I541I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr9:27294314 G>A maps to NM_020641.2 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr9:139927526 G>T maps to NM_207511.1 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr9:130922684 C>G did not map to a codon.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr9:135374152 C>T maps to NM_207417.1 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr9:97522563 C>T maps to NM_001193329.1 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:111881965 G>A maps to NM_032012.3 I76I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr9:132381853 G>A maps to NM_199350.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr9:4625443 G>A maps to ENST00000454239 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UB-01A-11D-A307-09 chr9:71155616 C>A maps to NM_153237.1 G38G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr9:27566947 T>C maps to NM_018325.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I3-01A-11D-A38Z-09 chr9:132597500 G>C did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr9:15578930 C>T maps to NM_173550.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr9:136270457 G>A maps to NM_153710.3 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr9:136269042 G>C did not map to a codon.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr23:15790631 A>G did not map to a codon.
Sequencing variant TCGA-DX-A7EO-01A-11D-A36J-09 chr8:61178600 C>T maps to NM_004056.4 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:35680960 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr13:49925038 G>A maps to NM_001079670.1 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:24483563 C>T maps to NM_012295.3 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr12:121098561 C>T maps to NM_001033677.1 F286F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr12:121094035 C>T maps to ENST00000453000 C141C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:67287291 G>A maps to NM_016366.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr19:13397419 G>A maps to NM_023035.2 S1154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:13346466 G>A maps to NM_023035.2 T1680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr19:13410061 G>A maps to NM_023035.2 N799N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr9:140852095 C>T maps to ENST00000277549 H431H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr9:140941367 C>T maps to ENST00000277549 F1143F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:2693780 C>T maps to NM_199460.2 A779A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:53845285 C>T maps to NM_001128840.1 P2113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:53778778 C>T maps to NM_001128840.1 I977I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A971-01A-11D-A387-09 chr3:53785792 C>T maps to NM_001128840.1 Y1178Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr1:181727997 C>A maps to ENST00000357570 G1533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:181549752 C>T maps to ENST00000357570 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:181701795 G>A maps to ENST00000357570 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr23:49068716 C>T did not map to a codon.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr23:49083119 G>A did not map to a codon.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr23:49074969 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr23:49065761 C>G did not map to a codon.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr23:49067929 C>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr17:48695413 G>A maps to NM_018896.3 G1744G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr16:1257369 C>T maps to NM_021098.2 F1001F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:40073416 G>A maps to NM_021096.3 G1642G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr1:201009018 G>A maps to NM_000069.2 S1854S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr7:81643715 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:54925445 C>T maps to NM_018398.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr3:55107537 C>G maps to NM_018398.2 L1018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr12:1988201 G>A maps to NM_172364.4 R522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QU-01A-11D-A27P-09 chr2:152727107 A>C maps to NM_000726.3 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:159163735 C>T maps to NM_021189.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HL-01A-11D-A387-09 chr19:44130153 C>G did not map to a codon.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr3:62578347 T>C maps to ENST00000383709 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U5-01A-11D-A228-09 chr3:62467516 C>T maps to ENST00000383709 V1018V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr3:62499311 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:62631500 G>A maps to ENST00000383709 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr6:7365793 A>G maps to NM_001170692.1 D700D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:15098930 C>T maps to NM_000728.3 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB35-01A-21D-A417-09 chr12:54117526 G>A maps to NM_020898.2 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2H-01A-11D-A38Z-09 chr7:93055784 G>A maps to NM_001164737.1 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:93108744 G>A maps to NM_001164737.1 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr10:105215260 G>A maps to NM_001001412.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A971-01A-11D-A387-09 chr1:1848445 C>T maps to NM_138705.2 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr5:149629833 C>T maps to NM_015981.3 E285E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr10:75599350 G>A maps to ENST00000423381 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A3OV-01A-11D-A228-09 chr3:49898703 C>T maps to NM_024046.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:49898673 G>A maps to NM_024046.3 F167F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr1:7723935 C>T maps to NM_015215.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UD-01A-11D-A307-09 chr1:6885150 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr17:4875805 C>T maps to NM_015099.3 S843S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:12858603 C>T maps to NM_001162499.1 Q725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr6:44147870 G>A maps to NM_007058.3 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr2:31000430 A>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr15:42678473 C>T maps to NM_000070.2 F163F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:15283683 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr12:75678835 G>A maps to NM_032606.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr17:38324173 C>T maps to NM_007359.4 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:73504325 C>T maps to NM_020753.3 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:202149905 G>A maps to NM_001080125.1 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr6:90576755 C>T maps to NM_012115.3 S1249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr6:90576104 C>G maps to NM_012115.3 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr1:116247890 G>T maps to NM_001232.3 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr3:122002846 G>A maps to NM_001178065.1 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:121980841 C>T maps to NM_001178065.1 F320F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:10703231 G>A maps to NM_001079843.1 R1335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A75J-01A-11D-A32I-09 chr1:10725139 C>A maps to NM_001079843.1 G169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB36-01A-11D-A417-09 chr11:65793081 G>A maps to NM_053054.3 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr11:65789004 C>A maps to NM_053054.3 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:92058304 C>T maps to NM_024764.2 R917R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr20:32217652 G>C maps to NM_005093.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr18:70205470 G>C maps to NM_182511.3 G205G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr21:37518519 G>T maps to NM_001236.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr21:37518767 A>T maps to NM_001236.3 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr9:122048 G>A maps to NM_018491.3 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr19:14024036 G>A maps to NM_017721.4 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr10:70531090 T>C maps to NM_018237.2 D809D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:89430580 G>A maps to NM_001008661.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:42906959 C>T maps to NM_001296.4 Y322Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:42906960 C>T maps to NM_001296.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr19:15132309 G>A maps to NM_173482.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr18:47778110 G>A maps to NM_145020.3 Q173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr4:186379435 G>A maps to NM_152775.3 R769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:48801541 G>A maps to NM_144577.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:68578735 G>A maps to NM_176816.3 F452F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr3:42781188 C>T maps to NM_144719.3 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr7:92902024 C>T maps to NM_017667.2 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A8JB-01A-23D-A37C-09 chr7:92938150 C>T maps to NM_017667.2 Q549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr22:42205935 C>T maps to NM_024821.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:42205973 C>T maps to NM_024821.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr2:179742828 G>T maps to NM_173648.3 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr17:16593773 C>T maps to NM_014695.1 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr17:16623535 A>G maps to NM_014695.1 E580E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr17:18511274 C>A did not map to a codon.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr7:76916776 G>A maps to NM_020879.2 K766K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr7:76866304 G>A maps to NM_020879.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:106166548 C>T maps to NM_001008723.1 Q752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A67I-01A-31D-A307-09 chr19:11537379 G>A maps to NM_145045.4 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U7-01A-11D-A29N-09 chr22:30768184 G>A maps to NM_001017437.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:30766812 C>T maps to NM_001017437.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:77290758 C>T maps to NM_001042784.1 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr1:159857723 C>T maps to NM_012337.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr1:159860313 T>C maps to NM_012337.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BN-01A-11D-A37C-09 chr23:49106183 C>A did not map to a codon.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr1:3679934 G>A maps to NM_152492.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:27362241 C>T did not map to a codon.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr17:42759384 C>G maps to NM_144609.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr3:48475278 A>G maps to NM_024661.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr12:111322002 G>A maps to NM_152591.1 T341T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:111345204 G>A maps to NM_152591.1 R539R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:52439834 C>T maps to NM_031290.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr17:32612892 C>T maps to NM_002986.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:45104165 C>T maps to NM_001029835.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr23:50055540 C>T did not map to a codon.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr15:43482567 G>C maps to NM_012142.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:2506846 C>T maps to NM_001761.2 S729S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K6-01A-11D-A21Q-09 chr12:49088155 G>A maps to NM_001240.2 Q281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr15:55677812 G>A maps to ENST00000442196 Q54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr3:46306889 C>T maps to NM_178328.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:32995834 G>A maps to NM_005508.4 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr3:32995906 C>T maps to NM_005508.4 Y331Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:45943137 C>T maps to NM_031200.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:33266334 G>A maps to NM_006584.3 F360F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HZ-01A-11D-A38Z-09 chr12:7636085 C>A maps to NM_004244.4 G989*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr12:7640491 C>A maps to NM_004244.4 G538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr1:158226588 C>T maps to NM_001763.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:158226672 G>A maps to NM_001763.2 W234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:158299202 C>T maps to NM_001764.2 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:71062846 G>A maps to NM_015717.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr19:7808071 G>A maps to NM_021155.3 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr19:7808041 G>A maps to NM_021155.3 D366D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr19:35832258 C>T maps to NM_001771.3 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:160811419 A>G maps to NM_001166663.1 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr1:160832437 G>C maps to NM_001166663.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr6:47573997 C>T maps to NM_012120.2 F505F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr19:45912056 G>A maps to ENST00000423698 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A8JB-01A-23D-A37C-09 chr19:45912296 G>A maps to ENST00000423698 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:135730453 G>A did not map to a codon.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr12:56120700 G>A maps to NM_001780.4 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:119263508 C>T maps to NM_005191.3 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr1:160549202 A>G maps to NM_001184879.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr19:14507286 T>C did not map to a codon.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr23:149984545 A>T did not map to a codon.
Sequencing variant TCGA-PC-A5DN-01A-12D-A27P-09 chr1:20915750 C>T maps to NM_001785.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr20:3782641 C>T maps to NM_021873.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr20:3781926 A>G maps to NM_021873.2 E244E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:110514443 T>C maps to NM_015891.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:227335251 G>A maps to ENST00000366766 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr22:19481885 C>T maps to NM_001178010.1 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:44394439 C>T maps to NM_001253.2 F624F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L4-01A-12D-A26G-09 chr1:91977216 T>A maps to NM_001134420.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr1:193181593 C>T maps to NM_024529.4 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr1:193181538 C>A maps to NM_024529.4 I362I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr8:25337453 G>A maps to ENST00000434814 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr12:6959715 C>A maps to NM_031299.4 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:45153653 C>T maps to NM_022842.3 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71O-01A-12D-A33E-09 chr3:45127315 G>T maps to NM_022842.3 S775S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr5:21854899 C>A did not map to a codon.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr5:21975455 T>C maps to NM_004061.3 K90K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr16:83813648 C>T maps to ENST00000268613 Y586Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I0-01A-11D-A38Z-09 chr18:64235824 A>G maps to NM_021153.2 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr20:60508133 C>A maps to NM_001794.2 R777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:60427859 C>T maps to NM_001794.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr20:60318790 C>T maps to NM_001794.2 D114D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr5:31323297 G>A maps to NM_004932.2 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr5:31323069 C>G maps to NM_004932.2 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr5:31317975 G>T maps to NM_004932.2 T609T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr18:63489323 C>A maps to NM_004361.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr18:63547709 C>T maps to NM_004361.2 I646I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:61935301 G>A maps to NM_001796.2 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr16:61687550 G>A maps to NM_001796.2 G787G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr5:26988428 G>T maps to NM_016279.3 Y4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr5:26988305 A>C maps to NM_016279.3 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr17:37627389 A>G maps to NM_016507.2 V435V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr7:40127770 A>T maps to NM_003718.4 R1026*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr9:90584818 G>A maps to NM_001039803.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr17:73998101 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:123165308 G>A maps to NM_018249.4 S1694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LW-01A-21D-A21Q-09 chr6:20781385 G>C maps to NM_017774.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr23:18668604 T>A did not map to a codon.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr23:18616675 C>G did not map to a codon.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr23:18627004 T>G did not map to a codon.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr9:21974781 C>T maps to NM_001195132.1 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr5:115151959 G>A maps to NM_001801.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr11:125867222 C>G maps to ENST00000392693 G747G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:139866051 G>A did not map to a codon.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr23:72667296 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr19:43031472 C>T maps to NM_001712.4 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr19:51981776 C>T maps to NM_001080405.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr19:51986520 C>G maps to NM_001080405.1 Y369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:51986562 C>T maps to NM_001080405.1 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr19:51981871 C>T maps to NM_001080405.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr19:45029179 A>T maps to NM_001102597.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr19:42085856 G>A maps to NM_001098506.1 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr19:42224050 C>T maps to NM_004363.2 D565D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr19:42224075 C>T maps to NM_004363.2 Q574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr19:43093684 G>A maps to NM_001816.3 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr19:43092963 C>T maps to NM_001816.3 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:37455747 G>A maps to NM_005760.2 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:37455746 G>A maps to NM_005760.2 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr22:18022399 G>A maps to ENST00000400579 V835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:18016891 C>T maps to ENST00000400579 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:18029071 C>T maps to ENST00000400579 S1344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr9:135941959 G>A maps to NM_001807.3 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr1:15788099 C>T maps to ENST00000375924 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:15788054 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:46787587 G>A maps to NM_014246.1 G2030G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:109812123 C>T maps to NM_001408.2 A2297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5Y9-01A-11D-A29N-09 chr1:109813850 C>T maps to NM_001408.2 L2537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr3:48700022 C>A maps to NM_001407.2 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr4:68357895 A>C did not map to a codon.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr4:104084677 C>T maps to NM_001813.2 K560K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UB-01A-11D-A307-09 chr4:104061059 G>A maps to NM_001813.2 S2030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EN-01A-11D-A38Z-09 chr5:68490471 A>C did not map to a codon.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr17:16256371 C>A maps to NM_181716.2 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr6:126661508 G>A maps to ENST00000368325 K30K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr4:56865762 T>C maps to NM_025009.3 D744D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:34092367 G>A maps to NM_007186.3 R2057R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr12:88508220 G>A maps to NM_025114.3 I676I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:88474096 C>T maps to NM_025114.3 Q1696Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr1:180010301 G>A maps to NM_014810.4 L1380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JK-01A-11D-A36J-09 chr1:179966059 C>T maps to NM_014810.4 D256D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:138219582 C>T maps to NM_024491.2 K454K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr5:639251 C>T maps to NM_018140.3 Q419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ET-01A-11D-A36J-09 chr9:80879142 T>C maps to NM_001098802.1 N513N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr16:57017286 C>T maps to NM_000078.2 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr1:196695645 T>C maps to NM_000186.3 N640N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A8OO-01A-11D-A36J-09 chr23:47486724 C>T did not map to a codon.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr7:117188765 C>T maps to NM_000492.3 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:117227800 C>T maps to NM_000492.3 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr1:151497205 A>G maps to NM_020770.2 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr2:27324339 G>A maps to ENST00000404694 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr10:50857625 G>A maps to NM_020549.4 W485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:146736134 C>T maps to NM_004284.3 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EO-01A-11D-A36J-09 chr17:7802798 G>T maps to NM_001005271.2 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:6692432 G>A maps to ENST00000309577 R1331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:6692433 G>A maps to ENST00000309577 A1330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:6204082 C>T did not map to a codon.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr20:40044279 T>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:40050120 G>A maps to NM_032221.3 S1718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K6-01A-11D-A21Q-09 chr8:61763140 G>T maps to NM_017780.2 E1832*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr14:21894402 T>G did not map to a codon.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr16:53191179 A>G maps to ENST00000219084 Q393Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XQ-01A-11D-A37C-09 chr16:53302009 A>G maps to ENST00000219084 G1563G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB30-01A-11D-A38Z-09 chr3:53857393 G>A maps to NM_018397.4 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr3:53857738 G>A maps to NM_018397.4 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N1-A6IA-01A-12D-A32I-09 chr19:16643458 G>A maps to NM_006387.5 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB36-01A-11D-A417-09 chr23:85282553 A>C did not map to a codon.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr3:87294949 G>A maps to NM_014043.3 Q71Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:175666463 G>A maps to NM_001822.4 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr2:220404161 G>T maps to NM_024536.5 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:109922647 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:74413852 C>T maps to NM_015424.3 W369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:136699926 G>A maps to NM_001006628.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:175618351 C>T maps to NM_001039523.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr15:32393541 C>T maps to NM_001190455.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:40337492 G>A maps to NM_017581.2 W3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr17:7360002 C>T maps to NM_000747.2 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:233396254 C>T maps to NM_000751.1 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:233399931 C>T maps to NM_000751.1 I488I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:233399030 G>A maps to NM_000751.1 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:233410305 G>A maps to NM_005199.4 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr2:101023036 C>G did not map to a codon.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr2:101014549 C>A maps to NM_004854.3 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr7:2473041 C>A maps to NM_018641.3 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr19:34263880 G>A maps to NM_022467.3 S396S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr2:26852316 C>T maps to NM_001029881.1 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:9918764 C>T maps to ENST00000430427 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MO-A47R-01A-11D-A24N-09 chr16:11016347 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:65496612 C>T maps to NM_003613.3 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:19655600 C>T maps to NM_153221.2 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr2:113513726 G>A maps to NM_152515.3 N407N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:106633617 G>A maps to NM_006825.3 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:106633475 G>A maps to NM_006825.3 Q379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:86959979 G>A maps to NM_001285.3 T597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EH-01A-11D-A24N-09 chr1:86913456 A>G maps to NM_006536.5 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B7-01A-11D-A307-09 chr7:143042675 C>T maps to NM_000083.2 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:170628343 T>C maps to NM_173872.2 F692F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:10182004 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:49853356 C>T did not map to a codon.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr16:1497075 G>C maps to ENST00000382745 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LU-01A-11D-A21Q-09 chr1:16360143 T>C maps to NM_004070.3 A685A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr23:106171470 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:11217639 G>A maps to ENST00000409790 L770L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:70208237 C>T maps to NM_173619.2 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:9840654 T>C maps to NM_001004419.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:8687362 C>T maps to NM_014358.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr2:71043555 G>A maps to NM_173535.2 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr4:141331037 G>T maps to NM_004362.2 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:73770746 C>T maps to NM_003388.4 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:178039426 C>T maps to NM_020666.2 E347E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:95679644 G>A maps to NM_024734.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:28502881 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr15:68504111 C>T maps to NM_017882.2 V129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:45491342 C>T maps to NM_001294.2 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:9795084 G>A maps to NM_001009566.1 F677F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:140178486 C>T maps to NM_022131.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:57758359 G>T maps to NM_004859.3 E1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr8:27468061 C>A maps to NM_001831.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr8:62212556 G>A maps to NM_173519.2 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr13:100518603 C>T maps to NM_206808.2 R249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr12:108685800 G>A maps to NM_001142344.1 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:47938974 G>A maps to NM_001142564.1 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:6265536 C>T maps to NM_001037329.2 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:21627714 G>A did not map to a codon.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr23:21627457 G>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:21549993 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:154751692 T>G maps to NM_173515.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:97463352 C>T maps to NM_020184.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr16:58568139 G>A maps to NM_016284.3 L1936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr6:88854276 C>T maps to NM_016083.4 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:3085330 C>T maps to NM_175607.1 I918I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr3:1415692 C>T maps to NM_014461.2 A677A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:1418689 C>T maps to NM_014461.2 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr7:148080942 C>T maps to NM_014141.5 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:146825906 G>A maps to NM_014141.5 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48U-01A-11D-A307-09 chr9:39178155 G>C maps to NM_033655.3 S247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr9:39099914 G>A maps to NM_033655.3 C996C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr9:39171378 C>T maps to NM_033655.3 R440R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:39118221 G>A maps to NM_033655.3 T705T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr16:76482697 C>A maps to NM_033401.3 V258V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:76587336 C>T maps to NM_033401.3 S1199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BV-01A-11D-A37C-09 chr2:125547485 G>A maps to NM_130773.2 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr7:51287559 G>A maps to ENST00000395542 H41H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr16:70530314 G>A maps to NM_015386.2 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr13:40253751 G>A maps to ENST00000255468 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:23457241 G>A maps to NM_153603.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr16:69368558 G>A maps to NM_032382.4 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A8OO-01A-11D-A36J-09 chr17:55028338 T>C maps to NM_004645.2 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr1:103345238 C>T maps to NM_080629.2 A1770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr6:33145926 A>T maps to NM_080680.2 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:33157100 G>A maps to NM_080680.2 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:33136328 C>T maps to NM_080680.2 G1309G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:75884928 G>A maps to ENST00000322507 L845L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr8:121301938 G>A maps to NM_021110.1 T1390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr1:32151242 T>C maps to NM_001856.3 K671K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U7-01A-11D-A29N-09 chr10:105798853 A>T maps to NM_000494.3 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr21:46908329 A>G did not map to a codon.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr21:46888375 C>T maps to ENST00000359759 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr21:46909413 G>A maps to ENST00000359759 V1061V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QT-01A-12D-A32I-09 chr17:48264175 G>A maps to NM_000088.3 G1213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A8OO-01A-11D-A36J-09 chr20:61952384 C>T maps to ENST00000326996 P1065P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr5:177683351 A>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:86590695 C>T maps to NM_152890.5 V441V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42W-01A-11D-A24N-09 chr7:7550730 T>C maps to NM_001037763.2 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr13:110857839 C>T did not map to a codon.
Sequencing variant TCGA-DX-A6B9-01A-12D-A32I-09 chr13:110831645 G>A maps to NM_001845.4 I772I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr13:110828797 C>A maps to NM_001845.4 G1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr13:110839582 C>A maps to NM_001845.4 G544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr13:111080929 C>T maps to NM_001846.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr5:74696028 C>A did not map to a codon.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr23:107924141 G>C did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr23:107898617 G>A did not map to a codon.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr23:107924117 T>A did not map to a codon.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr23:107415761 C>A did not map to a codon.
Sequencing variant TCGA-JV-A5VF-01A-11D-A29N-09 chr23:107422568 C>G did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr23:107424152 C>T did not map to a codon.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr23:107417803 C>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:10083624 G>A maps to NM_015719.3 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:10114285 C>T maps to NM_015719.3 K268K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr2:238285619 A>T maps to NM_004369.3 R955R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:238280873 C>T maps to NM_004369.3 L1262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr2:238280645 C>T maps to NM_004369.3 Q1338Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB35-01A-21D-A417-09 chr3:130098261 T>C maps to ENST00000312481 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:130289704 T>C maps to NM_001102608.1 D815D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:130292992 C>T maps to NM_001102608.1 F1057F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr3:48626117 G>A maps to NM_000094.3 V848V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr3:48622989 C>T maps to NM_000094.3 R1298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:48626426 G>A maps to NM_000094.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr20:61467645 C>T maps to NM_001853.3 V503V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:36310950 C>T maps to NM_014186.3 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr4:83978559 A>T maps to ENST00000503682 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr12:120942761 G>A maps to NM_032314.3 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr4:47625634 G>A maps to NM_006587.2 V831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3NK-01A-11D-A21Q-09 chr4:47625658 G>A maps to NM_006587.2 P823P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr16:4411428 C>T maps to NM_024535.3 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:4458229 G>A maps to NM_024535.3 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr16:84651170 G>A maps to NM_021149.2 D32D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr3:148928118 T>A maps to NM_000096.3 K148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr3:148601469 G>A maps to NM_001870.2 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr19:17040027 G>A maps to ENST00000443236 P1013P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr19:17086901 G>T maps to ENST00000443236 I663I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr19:17088327 A>T maps to ENST00000443236 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QT-01A-12D-A32I-09 chr19:17111250 C>T maps to ENST00000443236 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr20:34220146 G>A maps to NM_003915.5 Q137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr20:34214296 G>T maps to NM_003915.5 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr14:24543258 G>T did not map to a codon.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr12:39079416 A>G maps to NM_153634.2 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr12:69652406 A>C maps to ENST00000266679 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr22:51011374 G>T maps to NM_152245.2 S427S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr1:53666451 T>C maps to NM_000098.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr23:88009152 T>C did not map to a codon.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr10:125506533 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr4:8609139 G>A maps to NM_001014447.2 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr1:207760909 C>T maps to NM_000651.4 R1904*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr1:207753675 T>C maps to NM_000651.4 C1676C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr9:131862185 C>T maps to NM_000755.3 G348G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr1:197396671 C>A maps to NM_201253.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2P-01A-11D-A387-09 chr1:197398634 T>A maps to NM_201253.2 C911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr1:197398673 G>A maps to NM_201253.2 E924E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:46333925 G>A maps to ENST00000288400 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:167517277 G>A maps to NM_003851.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr4:5857891 C>T maps to NM_001014809.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:20026104 C>T maps to NM_016652.4 K377K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr1:17263171 C>T maps to NM_014675.3 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A240-01A-32D-A27P-09 chr1:159683596 C>T maps to NM_000567.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:99664460 G>A maps to NM_018058.4 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:153925793 C>T maps to NM_181715.2 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr22:25620892 C>A maps to NM_000496.2 I21I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr20:47707376 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr23:1407437 A>G did not map to a codon.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr23:1419413 T>C did not map to a codon.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr17:61950101 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9I0-01A-11D-A38Z-09 chr8:3008949 G>T maps to NM_033225.5 C2000*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BG-01A-11D-A307-09 chr1:34002678 C>T maps to ENST00000373381 T3234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:34166165 G>A maps to ENST00000373381 F1188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:34276406 G>A maps to ENST00000373381 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:34164452 G>A maps to ENST00000373381 S1235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr1:34312506 G>A maps to ENST00000373381 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:34209094 C>T maps to ENST00000373381 E613E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr8:113668386 A>G maps to NM_198123.1 Y1000Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:113323299 G>A maps to NM_198123.1 R2598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr8:113267507 C>T maps to NM_198123.1 W3337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr8:113275913 G>T maps to NM_198123.1 T3272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr4:70800428 G>T did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:1980162 C>T maps to NM_001319.6 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr15:75982847 G>A maps to NM_001897.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr3:47610659 G>A maps to ENST00000383738 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:47618963 G>A maps to ENST00000383738 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr3:47618466 A>T maps to ENST00000383738 L350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:39184659 G>A maps to NM_033027.3 F552F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr2:166535782 T>A maps to ENST00000409420 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr20:23728455 G>A maps to NM_001898.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr10:53457701 G>A maps to NM_015235.2 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr23:120009416 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr23:153881532 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:143965764 G>A maps to NM_198495.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2G-01A-11D-A38Z-09 chr10:126715437 C>A maps to NM_022802.2 L297L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr10:126686542 G>A maps to NM_022802.2 L725L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr10:126715773 A>T maps to NM_022802.2 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr18:77474692 G>A maps to NM_004715.3 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr15:44811493 G>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:80783007 T>A maps to ENST00000402739 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr10:68139075 G>T maps to NM_013266.2 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr5:11117588 C>T maps to NM_001332.2 A750A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr5:11236826 A>G maps to NM_001332.2 F579F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr5:11023047 C>T maps to NM_001332.2 G944G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr1:41467862 C>T maps to NM_001905.2 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:41475838 C>T maps to NM_001905.2 T566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr16:75257096 C>T maps to NM_001906.4 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:1778662 G>A maps to NM_001909.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DN-01A-12D-A27P-09 chr9:90343552 G>A maps to NM_145918.2 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J1-01A-11D-A21Q-09 chr11:70255964 C>T maps to NM_001184740.1 Q64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr10:16870802 C>A did not map to a codon.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr10:16873359 C>T maps to NM_001081.3 L3473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr10:16957151 G>A maps to NM_001081.3 Y2410Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr23:119672571 C>A did not map to a codon.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr23:119691848 T>G did not map to a codon.
Sequencing variant TCGA-MB-A8JK-01A-11D-A36J-09 chr23:119670865 C>G did not map to a codon.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr23:119694211 G>T did not map to a codon.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr6:43154706 C>T maps to ENST00000354495 Q421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:124591958 C>T maps to NM_022034.4 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr2:180819048 G>T maps to NM_020943.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:39307106 C>T maps to NM_001171174.1 E330E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr3:39307682 G>T maps to NM_001171174.1 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr3:39307454 G>C maps to NM_001171174.1 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr5:134907551 G>C maps to NM_004887.4 Y109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:45988818 C>A maps to NM_006564.1 C282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LT-01A-12D-A21Q-09 chr23:35969299 G>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:35944248 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr23:35937997 C>A did not map to a codon.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr23:37850228 G>T did not map to a codon.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr23:148628296 T>G did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:105875880 C>G did not map to a codon.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr23:105905497 C>T did not map to a codon.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr23:36117933 A>G did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:139038580 C>T did not map to a codon.
Sequencing variant TCGA-DX-A3U5-01A-11D-A228-09 chr6:84665136 C>T maps to NM_016230.3 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:84569506 G>A maps to NM_016230.3 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:54644983 G>A maps to NM_001031672.2 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr23:37642768 T>C did not map to a codon.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr23:37663303 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:172411075 C>T maps to NM_024843.3 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr5:156810367 G>A did not map to a codon.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr23:83128691 G>A did not map to a codon.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr15:74636133 A>G maps to NM_000781.2 S275S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr8:143958161 A>T maps to ENST00000377675 S316S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr8:143956670 C>T maps to ENST00000377675 Q464Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr8:143994864 T>C maps to NM_000498.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr8:143994115 G>A maps to NM_000498.3 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:75045533 G>A maps to NM_000761.3 R392R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr2:219647126 T>G maps to NM_000784.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr19:41387539 G>A maps to NM_000764.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:96447885 C>T maps to NM_000772.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:96495122 G>A maps to NM_000772.2 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:96541612 C>T maps to NM_000769.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:135350607 C>T maps to NM_000773.3 R337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:41704520 G>A maps to ENST00000301173 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EI-01A-11D-A33E-09 chr6:46518103 C>T maps to NM_016593.3 *470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr7:99355783 G>T maps to NM_017460.3 S495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:99367473 G>A maps to NM_017460.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:47610343 C>T maps to NM_001010969.2 H340H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:47280765 G>T maps to NM_001099772.1 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:47280915 G>A maps to NM_001099772.1 G351G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:15791084 C>T maps to NM_023944.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U5-01A-11D-A228-09 chr19:16008346 G>A maps to NM_001082.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:15636236 C>T maps to NM_173483.3 F30F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:47534385 C>T maps to NM_178134.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr1:47583591 A>T maps to NM_178134.2 K502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:42916564 C>T maps to NM_004391.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr23:77528982 G>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:49280956 G>T maps to NM_020377.2 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr4:4411343 C>T maps to NM_001040101.1 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:57480901 G>A maps to ENST00000371231 F399F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr23:85769346 C>T did not map to a codon.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr23:85404004 G>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:59112873 G>A maps to NM_016651.5 Q511Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A3OV-01A-11D-A228-09 chr14:59112534 G>A maps to NM_016651.5 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:59113233 G>A maps to NM_016651.5 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr14:59113170 G>A maps to NM_016651.5 K610K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr11:61508746 C>G maps to NM_006133.2 L699L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr11:61113887 C>T maps to NM_015533.3 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:90321073 C>T maps to NM_004938.2 Q1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr2:159651907 G>C maps to NM_001017920.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr4:100756842 C>T maps to NM_014395.2 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr9:136521766 C>A maps to NM_000787.3 I519I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:137882227 G>A maps to NM_016216.3 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2J-01A-11D-A387-09 chr23:125686012 G>T did not map to a codon.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr23:125299629 T>C did not map to a codon.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr4:17805188 A>G maps to NM_017741.3 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr8:88885860 C>T maps to NM_152418.3 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr8:88885851 C>T maps to NM_152418.3 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr14:69521401 G>A maps to NM_003861.2 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr1:160187382 C>T maps to NM_015726.3 *598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr23:27997690 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:27998917 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:27998918 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr23:27765612 C>A did not map to a codon.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr23:27766739 C>T did not map to a codon.
Sequencing variant TCGA-DX-A3UA-01A-12D-A307-09 chr23:27766327 C>T did not map to a codon.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr23:27765398 A>G did not map to a codon.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr23:27765823 C>A did not map to a codon.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr23:27765204 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr23:27766186 G>A did not map to a codon.
Sequencing variant TCGA-DX-A3U7-01A-11D-A29N-09 chr3:98536624 C>T maps to ENST00000326857 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr18:51053023 C>T maps to NM_005215.3 S1383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A67I-01A-31D-A307-09 chr11:6643465 C>G maps to NM_003737.2 L3147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A67I-01A-31D-A307-09 chr11:6653373 G>A maps to NM_003737.2 S1123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr4:155254431 G>A maps to NM_017639.3 H477H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:155191118 C>T maps to NM_017639.3 Q1715Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5YA-01A-11D-A29N-09 chr4:155156308 C>T maps to NM_017639.3 G2710G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr4:155156101 C>T maps to NM_017639.3 W2779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:2296867 G>A maps to NM_001919.3 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr3:36759570 G>A maps to NM_033403.1 D561D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:114449769 C>T maps to NM_022836.3 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr10:14950955 G>A maps to NM_001033855.1 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr13:95131425 G>C maps to NM_001129889.1 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LT-01A-12D-A21Q-09 chr23:110644348 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:110653471 G>T did not map to a codon.
Sequencing variant TCGA-DX-A3LW-01A-21D-A21Q-09 chr1:85787221 C>G maps to NM_012137.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr14:53522447 C>T maps to NM_001160148.1 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2H-01A-11D-A38Z-09 chr11:103908419 T>C maps to NM_001001711.2 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr1:162722975 C>G maps to NM_006182.2 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:162737118 G>A maps to NM_006182.2 W421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr2:118582578 C>T maps to NM_006773.3 R424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr16:70363934 G>T maps to NM_007242.4 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr23:134713793 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr9:32500869 G>A maps to NM_014314.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:169327142 C>T maps to NM_001012967.1 K1057K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr8:7340203 A>G maps to NM_152251.3 N40N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:76646 T>A maps to NM_153325.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr8:11853730 A>G maps to NM_001033019.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:140285448 C>T maps to NM_015689.3 K395K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:140273685 G>A maps to NM_015689.3 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr15:65982789 C>T maps to ENST00000443035 W1381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:153914692 G>A maps to NM_014856.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr1:153908533 A>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:24756993 C>T did not map to a codon.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr7:24784185 G>A maps to NM_001127453.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:117168794 G>A maps to NM_015404.3 P692P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:117168926 G>A maps to NM_015404.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr8:145541663 G>C maps to NM_012079.4 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr22:19055724 C>T maps to NM_005137.2 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LT-01A-12D-A21Q-09 chr22:19026587 C>A maps to NM_005137.2 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:14217732 G>A maps to NM_004080.2 A723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8C-01A-11D-A387-09 chr3:186015928 G>T maps to NM_001346.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr7:137080394 C>A maps to NM_004717.2 V1010V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr23:50134455 G>T did not map to a codon.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr23:50114723 T>C did not map to a codon.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr23:50213483 G>T did not map to a codon.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr23:50213246 T>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:55340801 C>T maps to NM_014762.3 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:71152340 G>A maps to NM_001360.2 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr2:169948326 C>T maps to NM_001142271.1 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:2209607 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:12130992 C>T maps to NM_018706.5 F242F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr6:30632763 C>A maps to NM_003587.4 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr20:37597727 A>G maps to NM_021931.3 T15T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:37650562 C>T maps to NM_021931.3 N526N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr20:37617496 C>T maps to NM_021931.3 G129G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BV-01A-11D-A37C-09 chr12:125436982 G>A maps to NM_032656.3 S943S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr23:96185819 C>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:96213055 C>T did not map to a codon.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr23:96354764 C>A did not map to a codon.
Sequencing variant TCGA-3B-A9HR-01A-11D-A387-09 chr21:47924313 G>C maps to ENST00000318711 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr12:51126228 C>T maps to NM_173602.2 S1297S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr12:51112504 T>G maps to NM_173602.2 A955A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr15:66599177 C>T maps to NM_001143688.1 R104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr4:107845149 G>A maps to NM_014421.2 Y247Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr8:13162757 G>A maps to NM_024767.3 F456F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr8:13357079 A>G maps to NM_182643.2 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr23:69699099 G>T did not map to a codon.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr17:7094059 G>A maps to NM_001365.3 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr20:35075161 G>A maps to ENST00000339266 A490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:39991282 G>A maps to NM_016941.3 W127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr2:172950515 C>T maps to NM_178120.4 H37H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5Y8-01A-11D-A29N-09 chr2:172952849 C>G maps to NM_178120.4 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr17:48070844 C>T maps to NM_005220.2 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr10:124336089 A>G maps to ENST00000368915 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr23:32407759 C>T did not map to a codon.
Sequencing variant TCGA-DX-A240-01A-32D-A27P-09 chr23:31462735 T>C did not map to a codon.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr23:31515002 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr23:32519916 C>A did not map to a codon.
Sequencing variant TCGA-DX-AB3B-01A-11D-A417-09 chr23:32328227 C>A did not map to a codon.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr23:32481569 G>T did not map to a codon.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr23:32663085 G>C did not map to a codon.
Sequencing variant TCGA-MB-A5Y9-01A-11D-A29N-09 chr23:32583995 A>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:31462632 G>A did not map to a codon.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr23:31200985 G>T did not map to a codon.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr5:78338140 C>T maps to NM_013391.2 Q386Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr9:1056544 G>T maps to NM_181872.4 E320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr9:990188 G>A maps to NM_021240.2 E201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HL-01A-11D-A387-09 chr5:118539112 G>A maps to NM_005509.4 K2615K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr5:118469961 G>T did not map to a codon.
Sequencing variant TCGA-MB-A5YA-01A-11D-A29N-09 chr15:51828630 C>T maps to NM_001174116.1 Q682Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr15:51828726 T>C maps to NM_001174116.1 R650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr3:52412621 G>C maps to ENST00000273600 G2401G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr12:124409667 G>A maps to NM_207437.3 Q3828Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr12:124363843 G>A maps to NM_207437.3 W2684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr7:21940718 C>T maps to NM_003777.3 P4473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr7:21628210 C>T maps to NM_003777.3 R644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr7:21757492 A>C maps to NM_003777.3 R2369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr7:21603912 A>G maps to NM_003777.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2IZ-01A-11D-A21Q-09 chr3:57443569 G>A maps to NM_178504.4 R1049*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:57443833 G>A maps to NM_178504.4 F992F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr17:76506477 C>A maps to ENST00000389840 S1404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A3PN-01A-11D-A228-09 chr17:76503584 G>A maps to ENST00000389840 L1509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr17:7640497 G>A maps to NM_020877.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:7734589 G>A maps to NM_020877.2 Q4139Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr17:7644168 C>G maps to NM_020877.2 Y516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr16:21030951 C>A maps to NM_017539.1 E2006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB30-01A-11D-A38Z-09 chr16:21049178 G>T maps to NM_017539.1 L1618L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K6-01A-11D-A21Q-09 chr16:20944658 G>A maps to NM_017539.1 S4056S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr5:13727741 C>T maps to NM_001369.2 W3969*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr5:13727765 C>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr5:13735347 G>A maps to NM_001369.2 R3885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr5:13770871 C>T maps to NM_001369.2 R3197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr5:13769641 C>A maps to NM_001369.2 E3230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QU-01A-11D-A27P-09 chr5:13766210 G>A maps to NM_001369.2 C3325C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V2-01A-11D-A32I-09 chr5:13770858 T>G maps to NM_001369.2 R3202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr2:84861701 C>T maps to NM_001370.1 D1530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr2:84822876 C>A maps to NM_001370.1 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:84831569 C>T maps to NM_001370.1 T992T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr2:196849354 C>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:196746610 G>A maps to NM_018897.2 R1957*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:196753050 C>T maps to NM_018897.2 K1779K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr6:38994430 G>T maps to ENST00000327475 T4596T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr6:38813372 G>A maps to ENST00000327475 K1611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr6:38862524 C>T maps to ENST00000327475 R2866*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:38877409 C>T maps to ENST00000327475 F3198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr6:38800096 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:38749100 G>A maps to ENST00000327475 W725*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr6:38980306 G>T maps to ENST00000327475 L4524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr17:11687747 G>A maps to NM_001372.3 L2651L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr17:11583112 C>T maps to NM_001372.3 S1131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:11795158 G>A maps to NM_001372.3 R3726R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr2:234652337 G>A maps to NM_001001394.3 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr7:108213493 C>A maps to NM_012328.2 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:22048457 G>A maps to NM_022365.3 Q413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:183582839 C>T maps to NM_018981.1 D9D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:183616418 C>T maps to NM_018981.1 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:6699996 C>T maps to NM_018198.3 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr8:66963818 C>T maps to NM_033105.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr1:65871754 C>T maps to ENST00000371069 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr1:84878059 C>T maps to NM_021233.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:6591238 G>A maps to NM_144666.2 W4288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:101716780 G>A maps to ENST00000342239 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A75J-01A-11D-A32I-09 chr19:10287969 C>T maps to NM_001130823.1 K189K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:31389084 G>A maps to NM_006892.3 E666E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:220246113 G>A maps to NM_012100.2 N394N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr23:117744375 C>A did not map to a codon.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr23:117677514 C>A did not map to a codon.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr5:169504796 C>T maps to NM_004946.2 S1650S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:169446039 C>T maps to NM_004946.2 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr5:169508870 C>T maps to NM_004946.2 I1771I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr3:51273842 T>A maps to NM_004947.4 L662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr1:63084513 G>T maps to ENST00000371140 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr9:371526 G>A maps to NM_203447.3 Q656Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr9:371451 G>A maps to NM_203447.3 V631V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr9:311952 G>A did not map to a codon.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr8:21767193 A>G maps to NM_003974.2 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr21:37617589 G>A maps to NM_005128.2 P1104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:30918952 A>T maps to NM_080870.3 G904G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N1-A6IA-01A-12D-A32I-09 chr16:89703958 C>T maps to NM_004413.3 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DK-01A-11D-A27P-09 chr16:89702772 G>A maps to NM_004413.3 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:65108976 C>T maps to NM_006268.3 R137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr14:73190400 C>G maps to NM_012074.3 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr7:154598775 C>T maps to NM_130797.2 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr7:154002608 G>A maps to NM_001936.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr7:154667714 C>T maps to NM_130797.2 D661D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:109027920 G>A maps to NM_138815.3 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EN-01A-11D-A38Z-09 chr19:32954860 C>G maps to NM_001172774.1 S511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr19:32927361 C>T maps to NM_001172774.1 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:97548027 T>A did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:98293694 G>A maps to NM_000110.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr2:27167528 A>G maps to NM_020134.3 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DL-01A-11D-A26G-09 chr2:74751280 C>A maps to NM_133637.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:113295127 G>A maps to ENST00000355319 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:100507639 T>C did not map to a codon.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr23:100515139 C>G did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:100513528 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:100513529 C>T did not map to a codon.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr23:100509888 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr21:41385062 C>G maps to NM_001389.3 L1979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr21:41496169 G>A maps to NM_001389.3 N1216N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr21:41416185 C>T maps to NM_001389.3 R1734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr21:42080623 G>A maps to NM_001389.3 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BK-01A-11D-A37C-09 chr11:117308033 G>A maps to NM_020693.2 C1568C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:117392046 G>A maps to NM_020693.2 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:117335656 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr8:120862620 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr6:116758474 G>A maps to NM_013352.2 W948*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr18:29122724 A>C maps to NM_001943.3 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A850-01A-11D-A351-09 chr18:29110996 C>T maps to NM_001943.3 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UD-01A-11D-A307-09 chr18:29040794 G>T did not map to a codon.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr18:28993105 C>T maps to NM_001134453.1 Q910*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr18:28979506 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr6:7568117 G>T maps to NM_004415.2 L415L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DX-A1KU-01A-32D-A24N-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DX-A8BH-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DX-A8BK-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr15:49917552 T>C maps to NM_001144955.1 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C7-01A-11D-A36J-09 chr12:113532614 C>T maps to NM_004416.2 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BK-01A-11D-A37C-09 chr15:45394057 C>A maps to NM_014080.4 L928L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:45386853 G>A maps to NM_014080.4 N1477N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr10:76797661 G>A maps to NM_001003892.1 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71P-01A-12D-A33E-09 chr5:172195869 G>A maps to NM_004417.3 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J1-01A-11D-A21Q-09 chr23:44703771 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:348135 G>A maps to ENST00000457386 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2G-01A-11D-A38Z-09 chr1:167097262 G>T maps to NM_001080426.1 S965S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr1:167095963 C>T maps to NM_001080426.1 N532N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr23:152915638 G>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:183884037 A>G maps to NM_004423.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr18:46645157 G>A maps to NM_017653.3 R568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr14:102493600 C>T maps to NM_001376.4 N2954N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr14:102505774 C>G maps to NM_001376.4 L3829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr14:102505584 C>G maps to NM_001376.4 L3818L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr14:102483132 C>T maps to NM_001376.4 Q2549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2H-01A-11D-A38Z-09 chr11:103025516 A>G maps to NM_001080463.1 Q1184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U7-01A-11D-A29N-09 chr2:44028000 C>T maps to NM_001193464.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:80583534 C>T maps to NM_130897.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr2:71896857 C>A maps to NM_001130987.1 V1922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:137790631 G>A maps to NM_173543.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr16:2284932 G>A maps to NM_004424.3 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:43638023 G>A maps to NM_001159936.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr13:50237242 C>A maps to NM_032565.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:233345430 G>A maps to NM_004826.2 A716A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr2:233350832 C>T maps to NM_004826.2 Q177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:11805392 C>T maps to NM_024693.4 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr3:172474879 C>T maps to ENST00000392692 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr2:109545697 T>A maps to ENST00000376651 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:67914701 C>T maps to NM_014329.3 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:67913637 A>C maps to NM_014329.3 T594T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr9:139760676 G>A maps to NM_003792.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr5:83362410 C>T maps to NM_005711.3 R222R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr20:57896080 G>T maps to NM_207034.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr12:93244994 C>T maps to NM_003566.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr12:93246072 C>T did not map to a codon.
Sequencing variant TCGA-IS-A3K6-01A-11D-A21Q-09 chr11:62327653 G>A maps to ENST00000378019 R398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr16:22274468 G>A maps to NM_013302.3 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:36338742 G>A maps to NM_030636.2 K546K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr17:28405480 C>T maps to NM_198529.3 L996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr22:44079698 G>A maps to NM_022785.3 I393I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EH-01A-11D-A24N-09 chr13:22067468 T>C maps to NM_152726.2 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr23:44008132 C>A did not map to a codon.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr8:132957002 G>A maps to NM_015137.3 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr8:132957050 G>A maps to NM_015137.3 E49E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr15:82450160 G>A maps to NM_024580.5 N641N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr17:42929916 G>A maps to NM_004247.3 Q859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:42937395 G>A maps to NM_004247.3 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UA-01A-12D-A307-09 chr4:110897310 G>A maps to NM_001963.4 W658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:110880579 G>A maps to NM_001963.4 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:13624541 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr23:13626472 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr7:55087059 T>C did not map to a codon.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr23:20156711 A>G did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr7:6068552 C>T maps to NM_014413.3 G481G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr8:141545617 G>A maps to NM_012154.3 I740I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr1:36316470 C>A maps to NM_017629.2 S765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:186502838 C>T maps to ENST00000440191 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:53427671 C>T maps to ENST00000438209 S354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:53427626 G>A maps to ENST00000438209 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr17:12917813 C>G did not map to a codon.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr22:37770665 G>A maps to NM_052906.3 H303H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr22:37769291 G>T maps to NM_052906.3 Y761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:18576665 G>A maps to NM_006532.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr15:44066406 T>C maps to NM_025165.2 R337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr20:45017814 G>A maps to ENST00000439931 N96N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr11:107535877 G>A maps to NM_018712.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:141446624 C>T maps to NM_153702.3 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr7:73442537 G>A maps to ENST00000358929 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr7:73470691 C>T maps to ENST00000358929 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:48511990 G>T maps to NM_022142.4 G23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr5:49701669 C>T maps to NM_198449.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr22:29611584 C>T maps to NM_133455.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr14:100402663 C>A maps to NM_001008707.1 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr2:42522362 C>T maps to NM_019063.3 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr14:89168804 G>A maps to ENST00000380664 Y741Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:6926612 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr19:6896475 C>T maps to ENST00000381407 Y54Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr19:14877107 G>T maps to NM_013447.2 C191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr2:73160998 G>A maps to NM_004097.2 K263K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr2:73161037 G>A maps to NM_004097.2 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:71509596 G>A maps to NM_031889.2 Q818Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:71500251 A>G maps to NM_031889.2 Q146Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QT-01A-12D-A32I-09 chr4:71508540 T>C maps to NM_031889.2 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JL-01A-11D-A36J-09 chr6:132014683 G>A maps to NM_005021.3 L444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:185038020 C>T maps to NM_153343.3 G281G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MO-A47R-01A-11D-A24N-09 chr22:40139964 C>A maps to NM_152512.3 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr9:140331642 G>A maps to NM_001033113.1 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr22:41513218 C>T maps to NM_001429.3 H41H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48K-01A-11D-A307-09 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:132551344 G>A maps to ENST00000333577 Q2896Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr2:46605045 C>T maps to NM_001430.4 F421F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:16460970 G>A maps to NM_004431.3 I558I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:16456749 G>A maps to NM_004431.3 S880S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr3:89391178 G>A maps to NM_005233.5 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr3:97198208 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr3:97439139 A>G maps to NM_001080448.2 E940E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr6:93953227 A>G maps to NM_004440.3 V971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr6:93967916 A>G maps to NM_004440.3 G670G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr6:94066666 G>A maps to NM_004440.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2IZ-01A-11D-A21Q-09 chr1:23111369 C>T maps to ENST00000400191 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LT-01A-12D-A21Q-09 chr1:23233389 C>T maps to ENST00000400191 S692S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr17:48617654 G>A maps to NM_017957.2 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr19:11489387 G>A maps to NM_000121.3 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr8:144946230 G>A maps to NM_031308.1 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:56276506 G>A maps to NM_000502.4 W409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr23:48688008 C>G did not map to a codon.
Sequencing variant TCGA-DX-A7EQ-01A-11D-A387-09 chr17:37864782 C>T maps to NM_004448.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr12:56480357 T>G maps to NM_001982.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr12:56486836 C>T maps to NM_001982.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:56468888 G>A maps to ENST00000460849 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr5:60198335 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr21:39817382 G>A maps to NM_001136154.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:20809072 C>T maps to NM_001142725.1 L683L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:124626139 C>T maps to NM_138961.2 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr12:53680599 C>T maps to NM_012291.4 V1360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr2:239040213 C>T maps to NM_194312.2 H953H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:103494922 A>T did not map to a codon.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr23:103495557 C>A did not map to a codon.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr23:103498854 T>C did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:56524693 G>A maps to NM_001184796.1 V184V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2H-01A-11D-A38Z-09 chr12:56522183 C>G maps to NM_001184796.1 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr7:158534290 C>T maps to NM_020728.2 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UC-01A-11D-A307-09 chr1:157062674 T>C maps to NM_001004341.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr3:185823485 C>A maps to NM_004454.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5Y8-01A-11D-A29N-09 chr3:185797766 G>A maps to NM_004454.2 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr19:7916384 G>A maps to NM_001159944.1 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:74019441 G>A maps to NM_001988.2 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:74007887 G>A maps to NM_001988.2 R845*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr17:74004698 G>A maps to NM_001988.2 D1529D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr14:69707774 G>A maps to NM_001193363.1 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr9:140267431 G>A maps to NM_017820.3 F129F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr2:72411238 C>G maps to NM_015189.1 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:72692417 C>T maps to NM_015189.1 K617K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr9:37784918 G>A maps to NM_016042.2 D41D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr8:28600610 C>T maps to NM_001440.2 A810A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB36-01A-11D-A417-09 chr6:133804183 G>A maps to ENST00000452339 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr6:65707519 G>A maps to ENST00000370616 I738I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr13:113803497 G>A maps to NM_000504.3 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr1:160970419 C>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:160970568 T>A did not map to a codon.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr11:46747682 G>T maps to NM_000506.3 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:169493087 C>T maps to ENST00000367796 W1953*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr1:169529885 G>A maps to ENST00000367796 D164D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:169524538 G>T maps to ENST00000367796 T333T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:169510970 C>T maps to ENST00000367796 Q1124Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr23:154197705 C>T did not map to a codon.
Sequencing variant TCGA-PC-A5DO-01A-11D-A26G-09 chr23:154158399 G>A did not map to a codon.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr23:154159233 T>G did not map to a codon.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr23:154124374 C>T did not map to a codon.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr23:138612958 A>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:82439335 C>T maps to NM_001105281.1 K89K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DL-01A-11D-A26G-09 chr6:123100971 G>C maps to NM_001446.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr11:61615734 G>C maps to NM_004265.2 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr1:51121152 T>C maps to NM_007051.2 Q235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr5:175919334 T>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:1877604 G>A maps to NM_031213.3 Y254Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:59059502 C>T maps to NM_147189.2 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr7:143417911 C>T maps to NM_001130026.2 V379V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48K-01A-11D-A307-09 chr22:45719208 G>A maps to NM_017911.2 E67E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr12:58168427 G>T maps to NM_206914.1 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr9:96318800 G>A maps to ENST00000333936 G832G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:96318680 C>T maps to ENST00000333936 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr23:54160394 A>T did not map to a codon.
Sequencing variant TCGA-JV-A5VE-01A-11D-A29N-09 chr23:133922772 C>G did not map to a codon.
Sequencing variant TCGA-JV-A5VE-01A-11D-A29N-09 chr23:133922771 C>A did not map to a codon.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr23:133930159 C>A did not map to a codon.
Sequencing variant TCGA-DX-A3UA-01A-12D-A307-09 chr23:63410104 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr13:51825712 G>A maps to NM_145019.2 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr8:139209758 C>A maps to NM_015912.3 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr8:139164695 C>T maps to NM_015912.3 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr8:139164707 T>A maps to NM_015912.3 S670S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr4:89660242 G>A maps to NM_014883.2 L834L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr4:89772180 A>G maps to NM_014883.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr1:55078383 C>A did not map to a codon.
Sequencing variant TCGA-DX-A6BH-01A-12D-A307-09 chr1:179783086 G>T maps to NM_173509.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr11:73122447 C>T maps to ENST00000064778 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:15255777 G>A maps to NM_001010924.1 V603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr2:75745209 G>A maps to NM_032181.2 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EK-01A-11D-A24N-09 chr6:119345392 C>A maps to NM_024581.4 E249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr12:49993262 G>C maps to NM_032130.2 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:35715856 C>T maps to NM_152481.1 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:91321245 T>G maps to NM_001145065.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48U-01A-11D-A307-09 chr18:10773614 C>T maps to NM_022068.2 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr18:10789249 C>A maps to NM_022068.2 E666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr3:58629401 G>A maps to NM_138805.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:58622107 C>T maps to NM_138805.2 G166G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr23:79698999 T>C did not map to a codon.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr23:34149684 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:34149600 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:34148169 G>A did not map to a codon.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr23:34148569 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr23:34961057 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr23:34962203 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:34961451 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr23:34961412 C>T did not map to a codon.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr23:37028798 C>A did not map to a codon.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr23:37027353 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:37027773 C>T did not map to a codon.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr23:37028952 C>A did not map to a codon.
Sequencing variant TCGA-MB-A5Y9-01A-11D-A29N-09 chr23:37027131 A>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr23:37027072 G>T did not map to a codon.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr23:37026658 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr23:37026573 G>A did not map to a codon.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr11:114452462 A>G maps to NM_001077639.1 S292S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr1:177249690 T>A maps to NM_021165.2 L460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr1:177245379 T>C maps to NM_021165.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr16:67575478 G>A maps to NM_001193523.1 W336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr9:139616578 G>A maps to NM_152421.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2J-01A-11D-A387-09 chr23:119425115 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr5:156589652 G>A maps to NM_130899.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr7:128356955 C>A maps to NM_032599.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr9:90535817 G>C maps to NM_001145124.1 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr8:124219459 G>A maps to NM_032899.4 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr19:49104466 G>A maps to NM_017708.3 R446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr22:40391372 C>T maps to NM_138435.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr22:40417725 C>T maps to NM_138435.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:18874836 G>T maps to NM_001039999.2 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr8:12042939 G>A maps to NM_001083537.1 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr8:12044261 G>A maps to NM_001083537.1 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr11:65340913 G>T maps to NM_001098785.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MO-A47R-01A-11D-A24N-09 chr8:124796720 G>T maps to NM_144963.2 E239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr16:85141484 C>A maps to ENST00000393246 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N1-A6IA-01A-12D-A32I-09 chr2:33812337 A>C maps to ENST00000395190 L192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr23:8764384 T>C did not map to a codon.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr16:89837021 C>T maps to NM_000135.2 T724T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BN-01A-11D-A37C-09 chr23:14862775 T>A did not map to a codon.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr23:14882868 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr9:97869347 C>A maps to NM_000136.2 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr9:97869346 C>A did not map to a codon.
Sequencing variant TCGA-IE-A4EH-01A-11D-A24N-09 chr9:35078227 G>A maps to NM_004629.1 H140H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr10:127585220 C>T maps to NM_145235.3 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr2:163031446 G>T maps to NM_004460.2 A633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr12:29449968 T>C maps to NM_018099.3 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr13:99043119 G>A maps to NM_005766.2 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr17:80053286 G>A maps to NM_004104.4 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V2-01A-11D-A32I-09 chr17:80049466 G>A maps to NM_004104.4 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:150776004 C>G maps to NM_006712.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I3-01A-11D-A38Z-09 chr4:187630312 G>T maps to ENST00000260147 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr4:187539626 C>A maps to ENST00000260147 E2708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:187524965 G>A maps to ENST00000260147 Q3575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr4:187554872 C>A maps to ENST00000260147 E1430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr4:187629481 G>A maps to ENST00000260147 Y500Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UA-01A-12D-A307-09 chr5:150920163 G>C maps to NM_001447.2 V3001V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr5:150932822 C>G maps to NM_001447.2 T1357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HJ-01A-11D-A387-09 chr11:92616272 C>T maps to ENST00000298047 D4217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr11:92531872 T>G maps to ENST00000298047 V1898V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB30-01A-11D-A38Z-09 chr11:92615943 G>T maps to ENST00000298047 E4108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:92523347 C>T maps to ENST00000298047 D1525D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr11:92623795 T>A maps to ENST00000298047 G4429G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr4:126373192 C>T maps to NM_024582.4 S3674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr22:45921482 C>T maps to ENST00000348697 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr14:92403474 C>T maps to ENST00000267620 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr15:48780436 G>A maps to NM_000138.4 D1070D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr15:48729274 C>G did not map to a codon.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr15:48704927 A>G maps to NM_000138.4 S2688S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:127681106 G>A maps to NM_001999.3 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:127674748 G>A maps to NM_001999.3 I1116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr19:8197970 G>A maps to NM_032447.3 T537T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr19:8131120 G>A maps to NM_032447.3 S2704S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr19:8194142 G>A maps to NM_032447.3 A717A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr19:8146269 C>T maps to NM_032447.3 L2436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr19:8193948 G>A maps to NM_032447.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr9:97321345 C>T maps to NM_003837.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr19:9929420 G>A maps to NM_017703.1 D23D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:102523909 A>G maps to NM_145032.3 N410N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr15:63893605 G>A maps to NM_203373.2 E155E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr5:15937162 C>T maps to NM_012304.3 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr9:37537586 G>A maps to NM_012166.2 I313I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr10:5979191 G>A maps to NM_032807.3 V1078V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:5959429 G>A maps to NM_032807.3 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr11:33773134 C>T maps to NM_012175.3 W248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:121340680 G>A maps to NM_016298.3 K135K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr1:16578256 G>A maps to NM_018994.1 F354F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:16578031 G>A maps to NM_018994.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr6:52957541 C>T maps to NM_012347.4 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr17:18653125 C>T maps to ENST00000395665 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J1-01A-11D-A21Q-09 chr17:18668117 T>G maps to ENST00000395665 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr4:153271228 C>T maps to NM_033632.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:117365892 T>C maps to NM_153348.2 F128F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:55385769 C>T maps to NM_002000.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KU-01A-32D-A24N-09 chr19:40392868 G>A maps to NM_003890.2 N2545N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr19:40396214 G>A maps to NM_003890.2 H2394H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:72553809 G>A maps to ENST00000409314 I618I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr1:157771768 G>A maps to NM_052938.4 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:157739746 C>T maps to NM_030764.3 W168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:157718701 G>A maps to NM_030764.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BE-01A-41D-A32I-09 chr1:157666076 G>A maps to NM_052939.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:157648535 C>T maps to NM_052939.3 E723E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:157514755 G>A maps to NM_031281.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23T-01A-11D-A26G-09 chr5:114860079 G>A maps to NM_020177.2 V593V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2IZ-01A-11D-A21Q-09 chr8:125113349 C>A maps to NM_001039112.2 G1632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr8:124968282 G>A maps to NM_001039112.2 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr8:124987394 C>T maps to NM_001039112.2 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:6088259 G>A maps to NM_017671.4 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:6096460 G>A maps to NM_017671.4 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr20:6096536 C>T maps to NM_017671.4 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:121943275 G>A maps to NM_001024613.2 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:35843210 C>T maps to NM_005303.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr9:95796884 C>T maps to NM_033086.2 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr12:32751499 C>T maps to NM_139241.2 R224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr3:14949205 C>T maps to NM_152536.3 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr5:44305141 C>T maps to NM_004465.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr23:137717812 G>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:137715092 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:102375267 C>T maps to NM_175929.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr12:4488549 G>A maps to NM_020638.2 Q67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:38314943 G>A maps to NM_001174067.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr8:38279354 G>A maps to NM_001174067.1 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr10:123279549 C>T maps to ENST00000351936 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:1807114 C>T maps to NM_000142.4 C482C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr5:176523680 C>T maps to NM_213647.1 L698L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr5:176520501 C>A maps to NM_213647.1 L449L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr5:176524619 C>T maps to NM_213647.1 H784H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr4:155526180 A>C maps to ENST00000407946 Y397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:17731904 G>A maps to NM_201552.1 Q124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2G-01A-11D-A38Z-09 chr4:153897250 T>C maps to NM_033393.2 D936D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A67I-01A-31D-A307-09 chr23:135291452 C>A did not map to a codon.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr1:38463097 G>A maps to NM_004468.3 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:97063566 C>T maps to NM_020482.4 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr18:34205613 G>T maps to NM_025135.2 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U6-01A-11D-A29N-09 chr9:133779552 G>A maps to NM_001145106.1 H428H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:133779525 C>T maps to NM_001145106.1 W437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:15381436 G>A did not map to a codon.
Sequencing variant TCGA-VT-A80J-01A-11D-A36J-09 chr6:76023330 A>G maps to NM_015687.2 D739D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:42935414 G>A maps to NM_001080472.1 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr17:39974735 G>A maps to NM_021939.3 K228K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr1:152330045 A>C maps to NM_001014342.2 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80J-01A-11D-A36J-09 chr1:152328365 G>C maps to NM_001014342.2 G632G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr9:84607868 T>C maps to NM_001001670.2 N828N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr23:153590143 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6BH-01A-12D-A307-09 chr23:153591106 C>T did not map to a codon.
Sequencing variant TCGA-DX-A7EI-01A-11D-A33E-09 chr23:153587438 C>G did not map to a codon.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr23:153588590 G>A did not map to a codon.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr23:153588250 A>T did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr23:153583285 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr23:153583395 T>C did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:58134559 C>T maps to NM_001164317.1 I2055I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:128498131 C>T maps to NM_001458.4 S2617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:128493886 C>T maps to NM_001458.4 I2160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QT-01A-12D-A32I-09 chr7:128483308 C>T maps to NM_001458.4 I859I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr14:86088592 T>C maps to NM_013231.4 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KU-01A-32D-A24N-09 chr20:14307795 G>A maps to NM_198391.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr5:180040030 C>T maps to NM_182925.4 P1137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr5:180030332 C>G maps to NM_182925.4 G1317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr5:180047284 C>T maps to NM_182925.4 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:43320529 C>T maps to NM_005892.3 Q686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr2:153494157 T>C maps to NM_052905.3 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2F-01A-11D-A387-09 chr2:153475472 G>A maps to NM_052905.3 E476E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2F-01A-11D-A387-09 chr2:153475499 G>A maps to NM_052905.3 K485K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2F-01A-11D-A387-09 chr2:153475622 G>A maps to NM_052905.3 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr12:50050264 G>T maps to NM_175736.4 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr23:147018108 G>A did not map to a codon.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr11:47776103 A>G maps to NM_015308.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr6:159650886 A>T maps to NM_032532.2 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr11:49207239 T>G maps to NM_004476.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr11:49208257 T>A maps to NM_004476.1 K193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr11:49194969 A>C maps to NM_004476.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr11:89405053 G>T did not map to a codon.
Sequencing variant TCGA-JV-A5VE-01A-11D-A29N-09 chr11:71850757 C>T maps to ENST00000442948 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:71850434 G>T maps to ENST00000442948 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr20:22562841 C>G maps to NM_021784.4 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr7:4722448 G>T maps to NM_001037165.1 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr17:80540672 C>T maps to NM_004514.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:2968196 C>T maps to NM_202002.1 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:26864306 G>A maps to NM_003593.2 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr23:70320987 G>T did not map to a codon.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr23:70320815 A>G did not map to a codon.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr23:49114811 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr23:49107858 A>G did not map to a codon.
Sequencing variant TCGA-DX-AB2G-01A-11D-A38Z-09 chr20:30432799 A>G maps to NM_004118.3 T182T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr20:30433003 G>A maps to NM_004118.3 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:30432508 G>A maps to NM_004118.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:30433189 G>A maps to NM_004118.3 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr4:79350247 G>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:79343053 C>T maps to NM_025074.6 I1526I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr9:14759899 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2G-01A-11D-A38Z-09 chr10:135439802 C>T maps to ENST00000443774 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr6:116289822 G>T maps to NM_002031.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A67I-01A-31D-A307-09 chr9:37744413 C>A maps to NM_014907.2 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:49371642 C>T maps to NM_001018071.3 L1203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8C-01A-11D-A387-09 chr10:49414886 G>T maps to NM_001018071.3 I567I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B7-01A-11D-A307-09 chr23:12736130 T>G did not map to a codon.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr23:12736509 C>T did not map to a codon.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr23:12736057 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:12736025 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:12712519 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr4:48569312 G>A maps to NM_015030.1 R1041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr4:48588693 A>T maps to NM_015030.1 I564I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr14:44974525 A>T maps to NM_032135.3 A555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr15:83430978 C>T maps to NM_001007122.2 W624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:49190276 G>A maps to NM_000145.3 I561I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr15:39910029 G>T maps to NM_152597.4 P535P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:186657367 G>A maps to NM_173651.2 S1924S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr2:186657268 C>A maps to NM_173651.2 L1891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:186673772 C>A maps to NM_173651.2 S6669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr5:132902895 A>G maps to NM_015082.1 F47F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr4:162307282 G>A maps to NM_020116.3 Y720Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:162307513 C>T maps to NM_020116.3 K643K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:24191982 C>T maps to NM_000147.4 K174K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr16:70503092 G>A maps to NM_145059.2 E274E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr23:44397735 C>G did not map to a codon.
Sequencing variant TCGA-DX-A6B9-01A-12D-A32I-09 chr5:39153560 C>T maps to ENST00000263405 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:46014637 G>A maps to NM_024513.2 Q161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B7-01A-11D-A307-09 chr2:208632892 T>A maps to NM_003468.3 K191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HL-01A-11D-A387-09 chr8:104336783 A>G maps to NM_003506.3 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr5:151183495 T>C maps to NM_198395.1 T415T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr9:101258769 C>T maps to NM_005458.7 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DL-01A-11D-A26G-09 chr5:161309576 A>G maps to NM_001127648.1 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:161113236 C>T maps to NM_000811.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr4:47427785 C>A maps to NM_000812.3 A392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr15:26793095 C>T maps to NM_021912.4 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:151123885 A>C did not map to a codon.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr4:46053587 A>C maps to NM_173536.3 S328S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A75J-01A-11D-A32I-09 chr15:27777804 C>T maps to NM_033223.4 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:89907896 G>A maps to NM_002042.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:26581850 C>T maps to NM_001134366.1 C505C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr10:26518624 C>T maps to NM_001134366.1 I253I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr4:862360 G>A maps to NM_005255.2 D787D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr4:870904 G>T maps to NM_005255.2 S649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr4:871533 G>T maps to NM_005255.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:30951977 G>A maps to NM_004861.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr17:73759479 T>G maps to ENST00000437911 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr9:101589136 G>C maps to NM_024642.3 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:155098680 C>T maps to NM_052917.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:155252642 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:31133826 G>A maps to NM_024572.2 I533I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr2:31167808 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:132905600 G>A maps to NM_001122636.1 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr4:173734826 C>A maps to NM_001034845.2 I292I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr18:74963118 C>T maps to NM_001480.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr5:57790368 G>A maps to NM_152687.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr12:100994197 T>C maps to NM_174942.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr23:48651598 T>C did not map to a codon.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr19:19612197 C>T maps to ENST00000404158 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:19612116 G>A maps to ENST00000404158 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr12:120884318 C>G maps to NM_176818.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:120884351 G>A maps to NM_176818.2 K23K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr22:30682026 G>A maps to ENST00000434291 I419I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr1:155205041 C>T maps to NM_001005742.2 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr3:81548344 T>C maps to ENST00000264326 E656E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:89585887 G>A maps to NM_004120.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:89582834 G>A maps to NM_004120.3 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:89835159 C>T maps to NM_198460.2 C82C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr2:237074886 G>A maps to NM_001485.2 G239G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:38203985 G>A maps to NM_001171690.1 G4G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:109100730 C>T maps to NM_181453.3 Q1193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr21:34109574 T>A maps to NM_016631.3 R876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr7:44189416 C>A maps to NM_000162.3 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:120580481 C>T maps to NM_006836.1 L1886L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr6:10529548 C>A maps to NM_145649.4 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LU-01A-11D-A21Q-09 chr15:59911093 G>A maps to NM_004751.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr15:59911069 A>G maps to NM_004751.2 E211E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:59911477 C>T maps to NM_004751.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:118462868 G>A maps to NM_017686.3 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr10:48438536 C>T maps to NM_004962.2 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr10:48429408 G>T maps to NM_004962.2 G159G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr12:7843123 G>A maps to NM_020634.1 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EK-01A-11D-A24N-09 chr12:7843091 G>A maps to NM_020634.1 T159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:34025453 G>A maps to NM_000557.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:34025452 G>A maps to NM_000557.2 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr23:153668461 C>G did not map to a codon.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr5:37834784 G>C maps to NM_001190468.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr23:69644893 C>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:69647165 C>G did not map to a codon.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr12:58008521 C>T maps to NM_001111270.1 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:17962839 G>T maps to NM_001130009.1 R787R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr5:137593566 G>A maps to NM_001496.3 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AK-01A-21D-A24N-09 chr6:55263987 C>A maps to NM_207410.2 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr17:4462704 G>A maps to ENST00000414312 N130N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr22:22989253 C>T maps to ENST00000215938 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr7:150325421 C>A maps to ENST00000438845 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:150327158 C>T maps to ENST00000438845 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J1-01A-11D-A21Q-09 chr7:150174546 C>T maps to NM_175571.2 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr7:150174546 C>T maps to NM_175571.2 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80J-01A-11D-A36J-09 chr20:25422335 A>G did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:14593635 G>A maps to NM_202470.1 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr1:39340984 T>C maps to NM_030772.4 Q262Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr23:70444047 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr13:20763342 G>A maps to NM_004004.5 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr15:35045371 A>G maps to NM_020660.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr3:33058209 G>A maps to NM_000404.2 N490N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr11:134241001 C>A maps to NM_138342.3 S439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:134244500 G>A maps to NM_138342.3 W571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:8125882 C>T maps to NM_138426.2 F453F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr9:131296041 A>G maps to NM_001003722.1 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr12:57865298 C>T maps to NM_005269.2 Q926*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:57859403 G>A maps to NM_005269.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr12:57864283 C>A maps to NM_005269.2 Y587*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr12:75728539 G>A maps to ENST00000378695 W11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr12:75737699 C>G maps to ENST00000378695 V134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr1:54059921 C>T maps to NM_147193.2 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr16:4387500 G>C maps to NM_032575.2 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:3828337 G>A maps to NM_001042413.1 T909T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr9:4118550 G>A maps to NM_001042413.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr6:39040727 C>T maps to NM_002062.3 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr5:151239458 G>A maps to NM_001146040.1 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JL-01A-11D-A36J-09 chr1:183933059 G>T maps to NM_015101.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:183914610 C>T maps to NM_015101.2 R408R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr12:104396989 G>T maps to NM_031302.3 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr19:48248836 C>T maps to NM_015710.4 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:1960164 G>A maps to NM_001500.2 F193F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr2:220371490 C>T maps to ENST00000373917 R465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:155649567 C>T maps to NM_003875.2 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:3094702 C>T maps to NM_002067.2 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr20:57466891 C>T maps to NM_001077488.1 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr3:50230724 G>T maps to NM_000172.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr22:23438605 G>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:30522612 G>A maps to NM_005275.3 F152F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr23:54578771 C>A did not map to a codon.
Sequencing variant TCGA-FX-A3NJ-01A-11D-A21Q-09 chr1:231411034 C>T maps to NM_014236.3 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:102160055 A>G maps to NM_024312.4 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr12:65130857 G>A maps to ENST00000418919 Q374*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr9:127660877 C>A maps to NM_002077.3 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr12:133351888 G>A maps to NM_005895.3 N1327N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UC-01A-11D-A307-09 chr15:75562506 C>T maps to NM_001164404.1 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QU-01A-11D-A27P-09 chr15:75557686 A>T maps to NM_001164404.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:75585480 G>A maps to NM_001145224.1 E523E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:121415177 T>A maps to ENST00000393667 K1398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr9:88655782 C>T maps to ENST00000376023 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr19:55530045 G>C maps to NM_001083899.1 S233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr19:55525953 T>C maps to NM_001083899.1 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr1:167025039 C>T maps to NM_005814.1 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:145140973 C>A maps to NM_003801.3 S604S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:33608774 C>T maps to NM_018025.2 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr1:46106025 T>C maps to NM_021639.4 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr23:132458180 C>A did not map to a codon.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr13:94482414 C>T maps to NM_005708.3 R110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr13:95055374 G>A maps to NM_005708.3 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr14:67647599 C>T maps to NM_020806.4 Y752Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:24447085 C>T maps to NM_001503.2 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2H-01A-11D-A38Z-09 chr23:136113604 C>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:132841941 C>T maps to NM_001136557.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr12:123200741 G>A maps to NM_006018.2 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:46977163 G>A maps to ENST00000283297 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr6:47649470 A>G maps to NM_153839.6 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr23:135431966 A>G did not map to a codon.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:135405421 C>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:135427471 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:135430741 C>T did not map to a codon.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr23:135427330 C>T did not map to a codon.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr23:135487943 T>C did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:26532943 G>A maps to NM_001145168.1 C1036C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr16:57609002 C>T maps to ENST00000349457 Y495Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr16:57601386 C>T maps to ENST00000349457 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:129518773 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:134942552 C>T maps to ENST00000368577 F947F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr10:134916199 G>T did not map to a codon.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr4:22404356 G>T maps to NM_145290.2 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr4:22389639 C>T maps to NM_145290.2 S1218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:142737079 C>T maps to NM_198569.2 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr14:59931122 G>A maps to NM_022571.5 G274G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:64056752 C>T maps to NM_001170726.1 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr23:9711637 C>T did not map to a codon.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr23:9728812 C>T did not map to a codon.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr23:9711676 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr3:154055901 G>A maps to NM_001038705.1 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:119887099 C>T maps to NM_153002.2 K408K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:25887095 C>T maps to NM_020752.2 S847S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr10:25464561 G>A maps to NM_020752.2 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr23:78427343 T>C did not map to a codon.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr17:36482851 C>A maps to ENST00000398597 L2201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:36484306 C>T maps to ENST00000398597 E1716E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr12:12815223 T>C maps to NM_006143.2 Q53Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr12:12815076 G>C maps to NM_006143.2 Y102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr6:167571124 C>T maps to NM_005299.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:167570890 G>A maps to NM_005299.2 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:51274789 C>T maps to NM_001506.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr23:41555918 C>T did not map to a codon.
Sequencing variant TCGA-DX-A3LW-01A-21D-A21Q-09 chr7:124404541 C>A maps to NM_005302.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr7:124386686 C>A maps to NM_005302.2 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr23:150345293 C>T did not map to a codon.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr23:150349082 G>A did not map to a codon.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr16:57691385 C>T maps to NM_005682.5 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:57697425 C>T maps to NM_005682.5 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr6:110300821 C>G maps to ENST00000414000 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr6:97247514 G>A maps to NM_030784.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:19017309 A>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:91701268 G>A maps to ENST00000238699 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr4:8588801 C>T maps to NM_080819.2 F268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LT-01A-12D-A21Q-09 chr4:8583113 G>A maps to NM_080819.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr23:41586872 C>A did not map to a codon.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr3:151011992 C>T maps to NM_023915.3 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:147416170 G>A maps to NM_016334.3 W125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr16:57719752 G>A maps to NM_170776.4 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HL-01A-11D-A387-09 chr5:90106133 T>C maps to NM_032119.3 D5019D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2G-01A-11D-A38Z-09 chr23:101970022 A>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:13061395 C>T maps to NM_003979.3 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr17:72443157 G>T maps to NM_022036.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr5:176025350 G>A maps to NM_052899.2 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr5:176025083 C>T maps to NM_052899.2 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:176026412 G>A maps to NM_052899.2 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr5:176025455 G>A maps to NM_052899.2 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr17:7216152 G>C maps to NM_004489.4 G302G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr8:145730242 G>A maps to NM_005309.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-A68Q-01A-11D-A307-09 chr8:145730423 C>T maps to NM_005309.2 D135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr6:28500187 T>C maps to NM_001509.2 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:54456136 C>T maps to NM_001008397.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr11:123479373 C>A maps to ENST00000456860 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr15:72454681 C>T maps to NM_001012642.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr22:40351884 C>T maps to NM_004810.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr2:11767166 G>A maps to NM_014668.3 A1462A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DO-01A-11D-A26G-09 chr2:11761062 C>T maps to NM_014668.3 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr8:102661669 C>T maps to NM_024915.3 D547D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J1-01A-11D-A21Q-09 chr5:153065888 G>A maps to NM_001114183.1 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B7-01A-11D-A307-09 chr5:152873486 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr5:153078446 C>G maps to NM_001114183.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr10:87482893 G>A maps to NM_017551.2 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr21:30959768 G>A maps to ENST00000327783 F570F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr1:37325618 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:42566691 G>A maps to NM_002088.3 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr16:10274088 C>T maps to NM_000833.3 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:13715941 C>T maps to NM_000834.3 T1410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr12:13906441 G>A maps to NM_000834.3 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr9:104433106 C>T maps to NM_133445.2 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr9:104449455 T>C maps to NM_133445.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr8:145065510 C>A maps to NM_001009184.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K6-01A-11D-A21Q-09 chr3:141535882 G>A maps to NM_139209.2 L551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:141499262 G>A maps to NM_139209.2 K220K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:47424920 C>T maps to NM_004491.4 R997*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:51751813 C>T maps to NM_000839.3 A842A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:51749375 G>A maps to NM_000839.3 E529E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr7:86415653 G>A maps to NM_000840.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr6:34003462 G>C maps to NM_000841.1 T808T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UD-01A-11D-A307-09 chr5:178413151 G>T maps to NM_000843.3 T701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:178413705 G>A maps to NM_000843.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:7728065 G>A maps to NM_181874.2 K907K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:7188272 G>A maps to NM_181874.2 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:16168572 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:16168571 G>A did not map to a codon.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr8:130760914 G>A maps to NM_031415.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr12:13243610 C>A maps to NM_001080555.1 E64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A67I-01A-31D-A307-09 chr23:51486908 G>A did not map to a codon.
Sequencing variant TCGA-DX-A48J-01A-21D-A307-09 chr6:52849260 C>A did not map to a codon.
Sequencing variant TCGA-DX-A6B7-01A-11D-A307-09 chr6:52705542 C>G maps to NM_153699.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr4:106763271 A>T maps to NM_001031720.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr14:77795515 C>T maps to NM_145870.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr1:89325833 G>A maps to NM_001514.5 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:124130027 C>T maps to NM_001516.3 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr16:27512568 C>T maps to NM_001520.3 E668E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr4:156643227 C>T maps to NM_001130684.1 G585G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KU-01A-32D-A24N-09 chr12:14827568 G>A maps to NM_004963.3 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:14792795 T>C maps to NM_004963.3 E719E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr17:7918812 G>T maps to NM_000180.3 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr23:108708523 G>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:189434015 G>A maps to NM_016315.2 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr7:65439343 G>A maps to NM_000181.3 V443V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr12:21716177 G>A maps to NM_021957.3 R309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr5:134724633 G>A maps to NM_138610.2 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:9324306 C>T maps to NM_004285.3 F585F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr20:7894821 C>T maps to NM_017545.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:39888487 C>T maps to ENST00000310778 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140056690 G>A maps to NM_002109.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr23:152721041 G>A did not map to a codon.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr5:156533779 T>C maps to NM_032782.3 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr11:5255645 A>C maps to NM_000519.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:5269675 G>A maps to ENST00000440157 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr23:11136722 G>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:153220526 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:153219587 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr23:153222932 C>T did not map to a codon.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr23:153224894 T>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:45262297 G>A maps to NM_021072.2 L800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UA-01A-12D-A307-09 chr19:616056 G>C maps to NM_001194.3 A751A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr15:73617296 T>G maps to NM_005477.2 G659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr23:48678567 C>T did not map to a codon.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr23:48682630 G>T did not map to a codon.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr7:18630035 A>G maps to NM_178425.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr15:50540513 C>T maps to NM_002112.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:22570532 G>A maps to NM_138574.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:73978824 C>T maps to ENST00000334988 E434E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr5:41007432 G>A maps to ENST00000296803 G1245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr5:41017988 C>T maps to ENST00000296803 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr12:66725160 G>T maps to NM_033647.2 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:84339338 A>T maps to NM_133636.2 V990V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:65390508 C>T did not map to a codon.
Sequencing variant TCGA-DX-A3U5-01A-11D-A228-09 chr11:93796821 G>A maps to NM_001098672.1 S188S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr11:93806289 A>G maps to NM_001098672.1 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr15:28478361 T>C maps to NM_004667.4 K1535K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr4:89574168 C>T maps to NM_014606.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A76Y-01A-11D-A351-09 chr4:89338622 C>T maps to NM_017912.3 I535I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:57232442 C>T maps to NM_003865.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LT-01A-12D-A21Q-09 chr1:91818855 C>T maps to NM_001017975.3 R562R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:81374338 G>A maps to NM_000601.4 H241H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr7:81381427 T>A maps to NM_001010934.1 *211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr14:100118631 G>A maps to NM_001127258.1 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A240-01A-32D-A27P-09 chr17:1961285 C>T maps to NM_001098202.1 N453N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr14:62187219 G>A maps to ENST00000394997 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:118997779 G>A maps to NM_198971.1 Q42Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr9:35813317 G>C maps to NM_032593.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr7:75228535 C>T maps to NM_005338.4 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:114483815 T>C maps to ENST00000426820 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LT-01A-12D-A21Q-09 chr6:27834758 C>T maps to NM_005322.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr6:27861356 T>A maps to NM_003527.4 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:26020938 G>A maps to NM_003529.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr6:26225735 G>A maps to NM_003532.2 V118V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ET-01A-11D-A36J-09 chr6:26104192 A>G maps to NM_003542.3 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr1:149783701 G>A maps to ENST00000427880 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr1:228612939 G>A maps to NM_003493.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr6:12161888 C>T maps to NM_002114.2 T2235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr1:42046087 T>A maps to NM_024503.3 K1461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr1:41976280 A>G maps to NM_024503.3 S2354S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:42048122 G>A maps to NM_024503.3 S782S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:234750474 C>T maps to NM_018410.3 Q317Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr10:71025433 C>T maps to NM_025130.3 C822C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr6:32975874 C>T maps to NM_002119.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:32548562 G>A maps to NM_002124.2 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr1:185902756 C>T maps to NM_031935.2 I543I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr1:186086747 G>C maps to NM_031935.2 L3947L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:186106678 C>T maps to NM_031935.2 T4544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr4:174253278 C>T maps to NM_002129.3 E194E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr23:150155662 T>G did not map to a codon.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr19:1080304 G>A maps to NM_012292.2 A585A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:1083180 G>A maps to NM_012292.2 G928G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr5:162918133 C>T maps to NM_001142556.1 Y714Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr5:162891727 G>C did not map to a codon.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr16:4559675 G>C maps to NM_001127205.1 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:36093707 C>T maps to NM_000458.2 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr1:12907989 G>T maps to NM_001013631.1 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:43882741 G>A maps to NM_001098204.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr19:39329655 C>G did not map to a codon.
Sequencing variant TCGA-DX-A2IZ-01A-11D-A21Q-09 chr4:83350510 G>A maps to NM_031372.2 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr1:60338567 G>A maps to NM_015888.4 A706A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr19:12874392 T>C maps to NM_013312.2 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr19:12874564 G>T maps to NM_013312.2 R619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr4:57516894 C>T maps to NM_001145460.1 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BE-01A-41D-A32I-09 chr17:46675272 G>A maps to NM_018952.4 F80F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr12:54333236 C>T maps to NM_017410.2 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BK-01A-11D-A37C-09 chr19:35551320 G>A maps to NM_182983.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr22:26849246 G>A maps to NM_022081.4 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:26861485 G>A maps to NM_022081.4 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr10:100481498 G>A maps to NM_021828.4 Q291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A3OV-01A-11D-A228-09 chr8:21983186 C>A maps to NM_005144.4 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:63235915 C>A maps to NM_054108.3 G133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:63233659 G>A maps to NM_054108.3 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:152193480 G>A maps to NM_001009931.1 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2S-01A-11D-A38Z-09 chr1:152187036 C>T maps to NM_001009931.1 Q2356Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr1:152191611 A>G maps to NM_001009931.1 H831H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr4:11401251 C>T maps to NM_005114.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:13400074 G>A maps to NM_006042.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:26146953 G>A maps to NM_006040.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr6:114383952 A>T maps to NM_153612.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr16:1961875 G>A maps to ENST00000454677 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:131762775 G>A did not map to a codon.
Sequencing variant TCGA-SI-AA8C-01A-11D-A387-09 chr13:97485013 T>A maps to NM_153456.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HL-01A-11D-A387-09 chr17:40705301 C>T maps to NM_000413.2 D86D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr5:118865587 G>T did not map to a codon.
Sequencing variant TCGA-DX-AB35-01A-21D-A417-09 chr12:57167822 G>T maps to NM_003725.2 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB35-01A-21D-A417-09 chr12:57167861 A>C maps to NM_003725.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LW-01A-21D-A21Q-09 chr1:120056736 C>T maps to ENST00000235547 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:120050143 G>A maps to ENST00000235547 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr1:119964750 G>T maps to NM_000198.3 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr9:115171211 C>T maps to NM_032303.4 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr20:3729965 G>C did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:65008992 C>T maps to NM_021979.3 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VF-01A-11D-A29N-09 chr1:161494964 C>A maps to NM_002155.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr1:22204711 G>A maps to NM_005529.5 S884S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr4:70897716 G>T did not map to a codon.
Sequencing variant TCGA-N1-A6IA-01A-12D-A32I-09 chr6:87725414 C>T maps to NM_000865.2 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr23:113965855 A>T did not map to a codon.
Sequencing variant TCGA-FX-A76Y-01A-11D-A351-09 chr7:154863028 C>T maps to NM_024012.2 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J4-01A-32D-A21Q-09 chr4:3137956 T>G maps to NM_002111.6 L901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr4:3215719 G>A maps to NM_002111.6 P2270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr4:3188391 C>T maps to NM_002111.6 S1645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr4:3214354 G>T maps to NM_002111.6 V2231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB30-01A-11D-A38Z-09 chr21:33371478 G>T maps to NM_014586.1 G709G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr23:53631665 A>G did not map to a codon.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr23:53573734 C>G did not map to a codon.
Sequencing variant TCGA-K1-A3PN-01A-11D-A228-09 chr23:53620559 T>C did not map to a codon.
Sequencing variant TCGA-PC-A5DO-01A-11D-A26G-09 chr23:53619439 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:50332649 C>T maps to NM_003549.2 W128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:70913256 A>G maps to NM_032821.2 L3499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB35-01A-21D-A417-09 chr16:70942291 C>T maps to NM_032821.2 T2752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr16:71009036 A>T did not map to a codon.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr11:118919433 C>T maps to NM_001130991.1 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr6:82911137 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr19:10401796 C>T maps to NM_003259.3 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr1:23885511 T>C did not map to a codon.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr15:78452498 C>T maps to NM_005530.2 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:2639477 C>T maps to NM_006899.2 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr23:153055182 G>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr17:41165590 C>T maps to NM_005533.4 F160F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr11:314331 C>T maps to ENST00000328221 F59F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:299457 C>T maps to NM_001025295.1 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VF-01A-11D-A29N-09 chr9:21481375 C>T maps to NM_176891.4 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:27682295 G>A maps to NM_015662.1 S912S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr20:42271198 C>T maps to NM_016004.2 Q401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr20:42275583 C>T maps to NM_016004.2 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BN-01A-11D-A37C-09 chr15:65628223 G>A maps to NM_004884.3 C160C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:47122426 G>A maps to NM_006546.3 K465K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr6:160461742 G>T maps to NM_000876.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:38610307 C>T maps to NM_001552.2 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr2:217559221 G>A maps to NM_000599.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr4:57907079 G>A maps to NM_001553.1 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr1:201166386 C>T maps to NM_001164586.1 C103C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:201174375 C>T maps to NM_001164586.1 D361D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr19:51827071 C>T maps to NM_001101372.1 G105G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J0-01A-11D-A21Q-09 chr23:130419396 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:130408684 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:130408743 G>C did not map to a codon.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:130408804 G>T did not map to a codon.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:130409007 G>T did not map to a codon.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:130408706 G>C did not map to a codon.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr11:18729765 A>G maps to NM_173588.3 H1025H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:18731162 C>T maps to NM_173588.3 W923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr21:41137759 T>C maps to NM_001080444.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:99007548 C>T maps to NM_201612.1 K289K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr19:18186634 G>A maps to NM_005535.1 F208F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5Y8-01A-11D-A29N-09 chr23:114248418 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:81592358 C>T maps to NM_172217.3 Q898*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr3:9972613 C>A maps to NM_153461.2 C529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr3:9944675 C>G maps to NM_153483.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:50436458 G>A maps to NM_001001694.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:103040418 C>T maps to NM_003853.2 F73F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:113820211 G>A maps to NM_173170.1 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr2:113676367 C>A maps to NM_014439.3 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr2:113786527 A>G maps to NM_173178.1 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BG-01A-11D-A307-09 chr23:29301311 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:29959897 A>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:105011098 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:113888655 T>A maps to NM_173841.2 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr16:28513295 C>T did not map to a codon.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr19:39789056 T>A maps to NM_172140.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BN-01A-11D-A37C-09 chr23:70328507 G>C did not map to a codon.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr16:3119355 A>G maps to ENST00000416912 *235W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr23:155239604 C>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:155239913 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:121712770 G>A maps to ENST00000344209 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:239098569 C>A maps to NM_030768.2 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr19:15234360 G>A maps to NM_006844.3 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:15230043 G>A maps to NM_006844.3 N328N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:15233757 C>T maps to NM_006844.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:128034580 G>A maps to NM_000883.3 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:76731936 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr10:105048131 C>T maps to NM_032727.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr1:62253619 T>G maps to NM_176877.2 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr11:61914293 G>C maps to NM_001040694.1 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr11:61897826 A>G maps to NM_001040694.1 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr14:105178792 C>G maps to ENST00000252520 S838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr14:105180849 C>T maps to ENST00000252520 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A76Y-01A-11D-A351-09 chr13:111371714 G>T maps to NM_005537.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr4:184431444 G>A maps to NM_001564.2 K61K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr12:6760371 T>A maps to NM_001127582.1 K247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr7:41729831 G>A maps to NM_002192.2 Q233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:57843513 C>T maps to NM_005538.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:206870121 A>T maps to NM_017759.4 L685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:206921090 G>A maps to NM_017759.4 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr2:99169398 C>T maps to NM_001134224.1 G443G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr1:38343970 C>T maps to ENST00000373026 W602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr19:7267848 G>A maps to NM_000208.2 C53C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr7:1535870 G>T maps to ENST00000389470 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BN-01A-11D-A37C-09 chr11:62415486 G>A maps to NM_030628.1 L689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr1:44415574 C>A maps to NM_014652.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr14:24655083 G>A maps to ENST00000458132 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr7:2627480 G>A maps to NM_152558.3 R338R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:51897110 C>T maps to NM_203424.1 Q74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:67709267 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:53268414 G>A did not map to a codon.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr12:66603233 A>T did not map to a codon.
Sequencing variant TCGA-N1-A6IA-01A-12D-A32I-09 chr1:209969875 T>A maps to NM_006147.2 K66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:209961785 G>A maps to NM_006147.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:209961872 G>A maps to NM_006147.2 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr14:24632707 C>A maps to NM_006084.4 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr19:44223831 C>T maps to NM_019612.3 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J4-01A-32D-A21Q-09 chr2:227662434 G>A maps to NM_005544.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr2:227662245 G>A maps to NM_005544.2 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr23:107979562 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr23:107976495 G>T did not map to a codon.
Sequencing variant TCGA-IW-A3M4-01A-11D-A21Q-09 chr23:107975898 G>A did not map to a codon.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr23:107977402 A>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:108958134 G>A maps to NM_213595.2 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr15:74425760 G>A maps to NM_001130137.1 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A75J-01A-11D-A32I-09 chr20:13279760 C>T maps to NM_080826.1 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68J-01A-11D-A307-09 chr20:13279760 C>T maps to NM_080826.1 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr7:16317840 G>C maps to NM_001101426.3 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr5:52183737 C>A maps to NM_181501.1 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr1:145528029 C>A maps to NM_003637.3 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr17:42457509 C>A maps to NM_000419.3 E538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr17:42461714 G>A maps to NM_000419.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J0-01A-11D-A21Q-09 chr12:56081766 C>T maps to ENST00000347027 L1101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr12:56091248 G>A maps to ENST00000347027 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr16:30490512 G>T maps to NM_002209.2 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JL-01A-11D-A36J-09 chr16:31338250 G>A maps to NM_001145808.1 V902V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr16:31339498 G>T maps to NM_001145808.1 E915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr16:31371383 C>T maps to NM_000887.3 V235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A75J-01A-11D-A32I-09 chr12:53589908 G>A maps to NM_000889.1 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:52820316 C>T maps to NM_002215.2 Q534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:7618663 C>T maps to ENST00000256861 W577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr10:7679437 C>T maps to ENST00000256861 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr23:54784925 A>G did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr5:156668657 C>T maps to NM_005546.3 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:4714889 C>T maps to ENST00000356617 Q755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr12:26784882 G>T maps to NM_002223.2 I950I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr12:26784933 G>T maps to NM_002223.2 L933L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr12:26755359 C>T maps to NM_002223.2 L1207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr6:33630707 C>T maps to ENST00000374316 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:24507679 G>A maps to NM_006277.2 C632C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:152883367 C>T maps to NM_005547.2 L365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr19:49245483 A>C maps to NM_182575.2 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr20:10627605 C>T maps to NM_000214.2 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr4:6066654 T>C maps to NM_001099433.1 T461T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr4:6082015 C>T maps to NM_001099433.1 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:146971249 C>T did not map to a codon.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr10:133930997 G>T maps to NM_001105521.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68J-01A-11D-A307-09 chr11:133938974 C>T maps to NM_032801.3 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:51009438 C>T maps to NM_138334.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr8:75227250 C>T maps to NM_020647.2 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr20:42788547 G>A maps to NM_020433.4 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr1:59248442 G>A maps to NM_002228.3 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:39925776 G>A maps to NM_021991.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr3:20153213 A>G maps to NM_003884.4 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8C-01A-11D-A387-09 chr1:15430616 C>T maps to NM_201628.2 I660I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DO-01A-11D-A26G-09 chr11:47594901 G>A maps to NM_018095.4 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:41766983 G>A maps to NM_032138.4 V470V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr1:111215811 G>A maps to NM_002232.3 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr19:49573847 T>A maps to NM_031886.2 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr19:50826790 G>A maps to NM_004977.2 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:119915567 C>T maps to NM_012281.2 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:49620662 G>T maps to NM_002237.3 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr1:210977434 G>T maps to NM_172362.2 Y512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr7:150642532 G>A maps to NM_000238.2 R1134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr12:49944059 C>G maps to NM_012284.1 V622V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr12:49948321 G>A maps to NM_012284.1 G707G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr14:63269299 C>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:63246478 C>T maps to NM_139318.3 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr17:21318836 C>T maps to NM_021012.4 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr17:68128479 G>A maps to NM_018658.1 S84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr21:39086811 C>T maps to NM_002240.2 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr14:90651109 C>T maps to NM_022054.2 D330D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:215259780 G>A maps to NM_001017425.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:39159487 G>A maps to NM_003740.3 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:39162038 G>A maps to NM_003740.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr6:39159186 G>A maps to NM_003740.3 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:65363171 C>T maps to NM_033347.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:178543387 G>A maps to NM_005832.3 Q23Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr12:70824429 T>C maps to NM_014505.4 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:18096153 C>T maps to ENST00000222249 F334F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:73904752 G>A maps to NM_001160133.1 R824R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:73751663 C>T maps to NM_001160133.1 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr1:196250097 G>A maps to NM_198503.2 D934D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:196398871 T>C maps to NM_198503.2 Q218Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr8:36644846 C>T maps to NM_001031836.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UC-01A-11D-A307-09 chr22:38870537 G>T maps to NM_016657.1 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr11:67013487 C>T maps to NM_012308.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr2:86705388 G>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:137766110 C>T maps to NM_016604.3 H1689H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:5077411 C>T maps to NM_015015.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A3PO-01A-11D-A21Q-09 chr1:202709870 G>A maps to ENST00000367264 P1041P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr23:53246346 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:53222216 G>A did not map to a codon.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr23:53239968 T>C did not map to a codon.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr23:53223902 C>G did not map to a codon.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr19:10610475 G>A maps to NM_203500.1 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr6:62757842 C>T maps to NM_152688.2 Q92Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:24900847 C>T maps to NM_015299.2 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr9:2833368 C>A maps to NM_014878.4 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr16:85694911 G>T maps to NM_014615.2 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ER-01A-11D-A36J-09 chr17:73484163 C>T maps to ENST00000375248 I187I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:197444871 G>A maps to NM_014687.1 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr14:105353080 C>T maps to ENST00000453495 G836G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr20:36625224 G>T maps to NM_014657.1 S975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr20:36640745 A>T maps to NM_014657.1 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:36641176 G>A maps to NM_014657.1 Q348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:4820925 C>T maps to ENST00000450194 A765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr18:46163007 G>A maps to NM_001142397.1 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:85112038 C>T maps to NM_014732.2 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr12:22677415 C>T maps to ENST00000446597 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr12:22697069 C>T maps to ENST00000446597 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr12:22697033 C>T maps to ENST00000446597 V17V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:46689388 C>T maps to NM_001142673.1 T368T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr18:8786055 C>T maps to ENST00000456698 H978H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr18:8718543 C>T maps to ENST00000456698 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr18:8825818 C>T maps to ENST00000456698 T1756T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr18:8825189 G>T maps to ENST00000456698 G1547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:105515910 C>T maps to NM_015275.1 V227V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A3OV-01A-11D-A228-09 chr9:34971555 C>T maps to NM_015297.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr23:118284426 C>A did not map to a codon.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr23:118221163 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9HR-01A-11D-A387-09 chr4:57180681 C>T maps to NM_020722.1 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A971-01A-11D-A387-09 chr4:57193906 C>A maps to NM_020722.1 A1213A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr4:57180906 G>A maps to NM_020722.1 E413E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:24833273 C>A maps to NM_019590.3 S1692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:138612977 C>T maps to NM_020340.4 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M4-01A-11D-A21Q-09 chr17:44144913 C>A did not map to a codon.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr17:44116419 G>A maps to NM_015443.3 R789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:72289797 C>T maps to NM_014431.2 Q148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:113755592 G>A maps to NM_020817.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr14:94066937 C>T maps to ENST00000393153 F1132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr14:93995661 T>A maps to ENST00000393153 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:94089059 C>T maps to ENST00000393153 S1849S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:94088138 G>A maps to ENST00000393153 K1542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BK-01A-11D-A37C-09 chr8:95556149 C>A maps to NM_015496.3 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr10:30316574 C>T maps to NM_020848.2 Q834Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A3PO-01A-11D-A21Q-09 chr2:226516262 G>A maps to NM_020864.1 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:226447296 C>G maps to NM_020864.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr4:1360146 G>T maps to NM_020894.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:35107785 G>A maps to NM_025182.2 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr19:7676959 G>A maps to NM_001080429.2 S554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr7:138554309 G>A maps to NM_001164665.1 P1583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BG-01A-11D-A307-09 chr10:118689408 T>C maps to NM_001127211.1 E321E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:180905670 C>T maps to NM_020950.1 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:180905045 C>T maps to NM_020950.1 L667L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr1:180905483 G>A maps to NM_020950.1 S813S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr18:43497656 G>A maps to NM_020964.2 L1076L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr4:175225411 A>G maps to NM_001145314.1 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UC-01A-11D-A307-09 chr1:233518138 C>T maps to NM_032435.2 V931V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr1:233482269 G>A maps to NM_032435.2 W296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HZ-01A-11D-A38Z-09 chr6:111588189 G>A maps to NM_153369.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:139701264 G>A maps to NM_001039374.4 E445E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr1:11983046 C>T maps to ENST00000376576 V511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr1:11983546 C>T did not map to a codon.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr3:113379808 G>A maps to NM_001009899.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr23:73961333 C>A did not map to a codon.
Sequencing variant TCGA-DX-AB35-01A-21D-A417-09 chr23:73961201 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr8:28974506 G>A maps to NM_015254.3 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr20:16360000 G>A maps to NM_024704.4 V882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr1:21036297 G>A maps to NM_020816.2 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr1:21042108 G>A maps to NM_020816.2 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:43013577 G>A maps to ENST00000438933 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr17:72339229 C>T maps to NM_153209.3 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr17:72339229 C>T maps to NM_153209.3 N129N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:241728727 G>T maps to ENST00000373308 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:241728729 C>G did not map to a codon.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr12:39745739 T>C maps to ENST00000395670 R504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr16:29815364 G>A maps to NM_007317.1 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr6:168443352 G>A maps to NM_030615.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr14:104640550 C>T maps to NM_015656.1 I699I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr14:104646006 C>A maps to NM_015656.1 A1843A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr14:104639374 C>T maps to NM_015656.1 C494C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:245772643 C>T maps to NM_018012.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B7-01A-11D-A307-09 chr9:86530368 A>C maps to NM_017576.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:51902211 G>A maps to NM_032559.4 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:51902397 G>A maps to NM_032559.4 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr20:30898717 C>T maps to NM_004798.3 R380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EH-01A-11D-A24N-09 chr23:69550143 G>A did not map to a codon.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr23:69595980 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr5:154395665 T>C maps to NM_001099293.1 N749N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr5:154394597 G>A maps to NM_001099293.1 Q393Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr5:154396338 C>T maps to NM_001099293.1 R974*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:170024464 G>A maps to NM_014970.2 R49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:145694171 C>T maps to NM_145754.2 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:55281319 C>T maps to ENST00000291633 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:55341612 C>T maps to NM_013289.2 F406F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:158064705 C>T maps to ENST00000368173 F706F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr1:158064642 C>T maps to ENST00000368173 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr4:55589795 C>T maps to NM_000222.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr4:39448829 T>C maps to NM_175737.3 T828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr11:66032512 G>A maps to NM_022822.2 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:126071534 C>T maps to NM_014079.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr19:16437823 C>T maps to NM_016270.2 H350H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QU-01A-11D-A27P-09 chr9:110249600 C>T maps to NM_004235.4 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr23:56276719 A>G did not map to a codon.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr23:56292122 C>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:117043923 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:117079472 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:47374753 C>T maps to NM_025010.4 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr22:20819154 G>T maps to NM_032775.3 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:239049493 C>T maps to NM_198582.3 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:239054441 G>A maps to NM_198582.3 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr23:86890735 C>A did not map to a codon.
Sequencing variant TCGA-DX-A23V-01A-11D-A29N-09 chr3:183211911 G>A maps to NM_130446.2 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr19:51537871 C>T maps to NM_019598.2 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr19:51330314 C>T maps to NM_017509.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr19:51411892 C>T maps to NM_004917.3 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A67I-01A-31D-A307-09 chr2:48734479 C>T maps to NM_001135629.2 Q681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr12:9754109 C>G maps to NM_002258.2 G57G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr10:134981791 C>T maps to ENST00000368572 F112F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr10:135013926 C>A maps to ENST00000368572 R986R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:135025212 C>T maps to ENST00000368572 L1365L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr3:186450324 C>T maps to NM_001102416.2 C264C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr12:123014669 C>T maps to NM_014708.4 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr12:123070190 T>C maps to NM_014708.4 F1181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr1:32625018 C>T maps to NM_012316.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:152733504 C>T maps to NM_001025231.1 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr2:88327568 C>A maps to NM_016618.1 E172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr16:3016140 T>C maps to NM_172229.1 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr12:53069192 G>A maps to NM_006121.3 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr17:38978608 A>G maps to NM_000421.3 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BV-01A-11D-A37C-09 chr17:39023144 C>T maps to NM_000223.3 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:39022966 G>A maps to NM_000223.3 R158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:39739692 C>T maps to NM_000526.4 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:39739832 C>T maps to NM_000526.4 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:39032615 G>A maps to NM_019010.2 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr17:39081633 G>A maps to NM_015515.3 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr17:38936016 G>A maps to NM_181537.3 R261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XQ-01A-11D-A37C-09 chr17:38935801 T>C maps to NM_181537.3 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr17:39623130 G>T maps to NM_002278.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A3PN-01A-11D-A228-09 chr17:39619136 G>T maps to NM_002278.3 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr17:39503389 G>A maps to NM_004138.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr17:39635724 C>T maps to NM_002280.4 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr17:39577806 C>T maps to NM_003770.4 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr12:52942538 G>T maps to NM_033448.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:53169173 C>T maps to NM_015848.4 K271K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M4-01A-11D-A21Q-09 chr12:52566025 G>T maps to NM_182507.2 I378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr12:52708513 G>A maps to NM_002282.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:52758846 G>A maps to NM_002283.3 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr21:46057633 T>C maps to NM_181688.1 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr21:46047915 C>A maps to NM_198690.2 C276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-A68Q-01A-11D-A307-09 chr21:46101927 G>A maps to NM_181686.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr21:46086449 C>T maps to NM_181684.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr21:31802670 C>T maps to NM_181600.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr21:31874390 G>A maps to NM_181611.1 N6N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr21:31654515 G>A maps to NM_001085455.1 C245C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr21:31654815 G>A maps to NM_001085455.1 L145L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DX-A1L1-01A-11D-A24N-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr11:1629045 G>A maps to ENST00000359229 C240C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:1651390 G>A maps to NM_001001480.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr21:31986097 G>A maps to NM_181602.1 F42F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr17:39411669 T>C maps to NM_030975.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:117977683 G>A maps to ENST00000339824 I509I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr12:118198925 C>T maps to ENST00000339824 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr12:118199246 C>T maps to ENST00000339824 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:118199038 G>T maps to ENST00000339824 R255R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr2:143743590 G>C did not map to a codon.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr2:143798010 G>A maps to NM_003937.2 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr23:153135043 T>C did not map to a codon.
Sequencing variant TCGA-DX-A3LU-01A-11D-A21Q-09 chr1:62672641 G>A maps to NM_019079.4 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LU-01A-11D-A21Q-09 chr1:62675987 G>A maps to NM_019079.4 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:130413987 C>T maps to NM_032438.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3NK-01A-11D-A21Q-09 chr18:6311561 G>A maps to NM_173464.3 D21D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr15:63419127 C>T maps to NM_032857.3 I165I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:201356224 G>A maps to NM_005558.3 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr19:54866933 T>C maps to NM_002287.3 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KU-01A-32D-A24N-09 chr19:55019148 G>T maps to NM_002288.3 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A76Y-01A-11D-A351-09 chr18:7050761 G>T maps to NM_005559.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr6:129618897 G>A maps to NM_000426.3 K975K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr6:129380935 C>T maps to NM_000426.3 H97H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr6:112512892 A>T maps to NM_001105206.1 C221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr20:60937453 A>T did not map to a codon.
Sequencing variant TCGA-DX-A7ER-01A-11D-A36J-09 chr7:107601659 C>T maps to NM_002291.2 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2S-01A-11D-A38Z-09 chr7:107577717 G>A maps to NM_002291.2 L1256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:49161902 C>T maps to NM_002292.3 W1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr7:107732112 G>A maps to NM_007356.2 Y553Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:183086566 C>T maps to NM_002293.3 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BV-01A-11D-A37C-09 chr1:183212349 C>T maps to NM_005562.2 Q1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JK-01A-11D-A36J-09 chr9:133954580 C>T maps to ENST00000355048 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:133927959 C>T maps to ENST00000355048 L571L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr3:182871757 C>A maps to NM_014398.3 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr1:31210525 C>T maps to NM_006762.2 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr2:169571587 A>C maps to ENST00000392687 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr6:80198914 G>A maps to NM_181714.3 Q373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr1:152659591 C>T maps to NM_014357.4 C91C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:32742049 G>A maps to ENST00000373562 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr15:43622561 A>T maps to NM_014793.4 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:139658889 C>A maps to NM_203347.1 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr13:46717442 C>T maps to NM_002298.4 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M4-01A-11D-A21Q-09 chr5:169685120 G>A maps to NM_005565.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:33752144 G>A maps to NM_181336.3 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:154966127 C>T maps to NM_018655.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A75J-01A-11D-A32I-09 chr19:54967913 C>A maps to ENST00000431846 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr15:52246733 T>C maps to NM_138792.2 E428E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr17:76967849 G>A maps to NM_005567.3 A522A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr10:95537147 G>A maps to NM_005097.2 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HL-01A-11D-A387-09 chr12:71955559 G>C did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:48950634 C>A maps to NM_000233.3 G166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr23:111914309 G>A did not map to a codon.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr23:111914310 A>G did not map to a codon.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr3:9547831 G>A maps to NM_198560.2 T154T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:35773749 G>A maps to NM_182548.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr17:35300103 C>T maps to NM_005568.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr17:35299570 C>T maps to NM_005568.3 A250A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr12:113906051 G>T maps to NM_022363.2 T185T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr5:38530657 G>C maps to NM_002310.5 S31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:108863298 G>A maps to NM_001098268.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:55107113 G>A maps to NM_006863.1 K224K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:54802113 G>A maps to ENST00000251375 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EI-01A-11D-A33E-09 chr19:54844968 C>T maps to NM_012276.3 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr19:55144623 G>A maps to ENST00000427581 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:54783793 C>T maps to ENST00000391747 W86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr19:55179187 G>T maps to ENST00000391733 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:55177329 C>T maps to ENST00000391733 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr19:55179127 A>T maps to ENST00000391733 K363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr19:54759173 G>A maps to NM_001081442.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr19:54760200 G>A maps to NM_001081442.1 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:54760616 G>A maps to NM_001081442.1 T30T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr4:41607963 C>T maps to NM_014988.2 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr7:73511492 G>A maps to NM_002314.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr7:73535504 C>T maps to NM_002314.2 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr15:77907555 C>T maps to NM_032808.5 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr15:77908077 G>A maps to NM_032808.5 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr19:42912444 C>T maps to NM_005357.2 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:90490888 A>C maps to NM_001080518.1 R125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr15:75108828 G>A maps to NM_021819.2 W131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr2:97373088 G>T maps to NM_001142292.1 I328I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr22:50942779 A>C maps to NM_033200.2 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr13:76395652 A>T maps to ENST00000357063 K780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr13:76374986 C>T maps to ENST00000357063 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr7:97823853 C>T maps to NM_014916.3 F1359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr7:97770731 T>C maps to NM_014916.3 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:49013394 C>T maps to NM_001080434.1 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:165182895 G>A maps to NM_177398.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:165175182 G>A maps to NM_177398.3 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr5:135188364 C>T maps to ENST00000420621 C92C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr5:135188460 G>T maps to ENST00000420621 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr5:135188286 C>T maps to ENST00000420621 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr19:40172708 G>A did not map to a codon.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr10:105006437 T>A maps to NM_001143909.1 *229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr19:19260124 C>T maps to ENST00000410050 Q56Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr23:118124512 C>G did not map to a codon.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr23:118124457 A>T did not map to a codon.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr1:153233505 C>T maps to NM_000427.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71O-01A-12D-A33E-09 chr1:153234264 C>T maps to NM_000427.2 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A8OO-01A-11D-A36J-09 chr8:23225663 G>A maps to NM_002318.2 H67H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr10:100022500 C>T maps to NM_032211.6 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr6:161010661 A>T maps to NM_005577.2 V1290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr1:85331338 G>A maps to NM_012152.2 I155I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr5:1463891 C>T maps to NM_024830.3 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:82372859 C>T maps to ENST00000370717 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr17:56342327 C>T maps to NM_006151.2 V504V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr17:56343550 G>A maps to NM_006151.2 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr9:104086317 G>A maps to NM_017753.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr1:99422182 G>A maps to NM_001037317.1 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr23:114347860 C>G did not map to a codon.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr23:114357668 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr11:799455 G>T maps to NM_145886.3 R862R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3B-01A-11D-A417-09 chr14:42356844 C>T maps to NM_152447.3 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr19:4538292 G>A maps to NM_052972.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:113637278 C>T maps to NM_014813.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr12:57593004 G>A maps to NM_002332.2 Q3229Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr12:57594261 G>A maps to NM_002332.2 W3351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr12:57595283 G>A maps to NM_002332.2 E3450E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr12:57600487 C>T maps to NM_002332.2 H3941H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr2:141762961 G>A maps to NM_018557.2 G815G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr2:141625270 G>C maps to NM_018557.2 T1489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr2:142567932 G>A maps to NM_018557.2 H40H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr2:141201917 C>T maps to NM_018557.2 E3425E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:141214170 G>A maps to NM_018557.2 V3272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:142238082 G>A maps to NM_018557.2 I75I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr2:170163908 T>C did not map to a codon.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr2:170089919 C>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:170050304 C>T maps to NM_004525.2 G2932G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr2:170060690 G>C maps to NM_004525.2 G2602G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr2:170012823 C>A maps to NM_004525.2 T4037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr19:33697151 C>T maps to NM_002333.3 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:46905441 G>A maps to ENST00000256991 I909I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:53724099 A>G maps to NM_004631.3 C700C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:25492027 C>T maps to NM_017640.5 S378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr14:24525876 C>T maps to NM_138360.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr10:72083655 C>A maps to NM_207119.1 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:99892628 G>A maps to NM_144598.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr21:45877036 C>T maps to NM_030891.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr18:7231499 C>T maps to NM_001105581.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr18:7231228 C>T maps to NM_001105581.1 D31D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr18:7231237 G>T maps to NM_001105581.1 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr18:7232041 A>T maps to NM_001105581.1 *302C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr18:7231876 C>A maps to NM_001105581.1 L247L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:46744894 G>A maps to ENST00000254454 F704F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr1:54427719 C>T maps to NM_052940.3 I246I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr17:45914248 C>T maps to NM_033413.3 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VD-01A-42D-A38Z-09 chr17:17896104 C>T maps to NM_031294.3 C157C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr16:84203831 G>A maps to NM_178452.4 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr16:84203705 G>A maps to NM_178452.4 S424S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr11:554104 G>A maps to NM_198075.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:541616 G>A maps to NM_198075.3 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:70486802 G>A maps to NM_020794.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:70225938 C>T maps to NM_020794.2 R18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr9:131670724 C>T maps to NM_001127244.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr1:90180396 C>G maps to NM_032270.4 Y756*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr19:7963871 G>A maps to NM_025061.3 K155K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A8OO-01A-11D-A36J-09 chr3:37096645 A>G maps to NM_006309.2 N627N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr12:85638643 A>G maps to NM_001079910.1 R1698R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr12:85546890 G>A maps to NM_001079910.1 L1503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr1:74648302 T>A maps to NM_001105659.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr15:101554525 C>T maps to NM_024652.3 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr15:101464887 G>A maps to NM_024652.3 P17P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr12:40704300 C>T maps to NM_198578.3 R1462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr12:40692940 G>A maps to NM_198578.3 L1126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr12:40692909 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:204587479 G>A maps to NM_201630.1 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DN-01A-12D-A27P-09 chr2:77745758 G>A maps to NM_001134745.1 G412G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr12:1943688 G>A maps to NM_001163926.1 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:1940155 C>T maps to NM_001163926.1 F41F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr11:71817089 C>G maps to NM_001145309.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr19:35758743 G>A maps to NM_205834.2 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr21:47635207 G>A maps to NM_002340.5 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr2:33589421 C>T maps to ENST00000354476 N1514N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:33359995 C>T maps to ENST00000354476 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr14:74995276 C>T maps to NM_000428.2 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr1:23420543 G>T maps to NM_001142546.1 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr23:114541123 C>T did not map to a codon.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr2:160717367 C>T maps to NM_001198759.1 Q744Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr1:160771613 C>T maps to NM_001033667.1 I163I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr8:56922482 C>T maps to NM_002350.2 D451D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr8:143846100 G>T maps to NM_023946.2 C106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M4-01A-11D-A21Q-09 chr1:235950616 G>T maps to NM_000081.2 S1582*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr11:10580736 G>C maps to NM_006691.3 S297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr10:30900940 C>T maps to NM_183058.2 K176K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr22:21336824 G>C maps to NM_006767.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:36049198 A>T maps to NM_005584.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N1-A6IA-01A-12D-A32I-09 chr1:39888563 G>T maps to ENST00000361689 E3319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:39800359 A>G maps to ENST00000289893 K1140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr1:39752956 G>T did not map to a codon.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr1:39798400 G>A maps to ENST00000289893 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr20:15866409 C>T maps to ENST00000310348 D243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr7:1938009 C>T maps to NM_003550.2 V608V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B9-01A-12D-A32I-09 chr23:152482245 C>T did not map to a codon.
Sequencing variant TCGA-K1-A3PN-01A-11D-A228-09 chr23:148798424 G>A did not map to a codon.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr23:148797279 C>T did not map to a codon.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr23:151092442 G>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:151869462 G>A did not map to a codon.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr23:30269612 C>T did not map to a codon.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr23:30269230 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:27839440 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr23:35821012 G>T did not map to a codon.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr23:35820763 T>A did not map to a codon.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr23:26158105 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:26157606 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:26157982 C>T did not map to a codon.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr23:30236778 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:30236747 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr23:30260294 C>T did not map to a codon.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr23:26211981 A>G did not map to a codon.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr23:140996580 A>G did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:140996003 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:140994313 T>C did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:140993290 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr23:140994548 C>A did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:140994127 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:140995997 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr23:140994945 G>A did not map to a codon.
Sequencing variant TCGA-UE-A6QT-01A-12D-A32I-09 chr23:140996611 C>T did not map to a codon.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr23:140996391 G>A did not map to a codon.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr23:140996474 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:140967030 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2H-01A-11D-A38Z-09 chr23:140983152 G>A did not map to a codon.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr23:140953332 G>T did not map to a codon.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr23:140985391 T>A did not map to a codon.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr23:51639865 T>A did not map to a codon.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr23:51640321 T>C did not map to a codon.
Sequencing variant TCGA-K1-A42W-01A-11D-A24N-09 chr23:51637743 G>C did not map to a codon.
Sequencing variant TCGA-VT-A80J-01A-11D-A36J-09 chr23:51638172 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr23:75004714 T>G did not map to a codon.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr23:75003966 G>A did not map to a codon.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr15:23890951 C>T maps to NM_019066.4 E646E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr7:78636523 T>A did not map to a codon.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr7:77764398 G>A maps to NM_012301.3 D990D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr23:49022647 G>T did not map to a codon.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr5:179196020 G>A maps to NM_014757.4 R634R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr5:179196071 G>A maps to NM_014757.4 Q651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr4:140811110 C>T maps to ENST00000509479 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr4:140811065 C>T maps to ENST00000509479 Q508Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr4:140811110 C>T maps to ENST00000509479 Q493Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr23:149639408 A>T did not map to a codon.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr23:149671638 G>T did not map to a codon.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr5:109110494 G>T maps to NM_002372.2 R401R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:75658861 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr6:96054070 C>T maps to NM_024641.2 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr6:96034834 A>T maps to NM_024641.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr23:43571983 T>C did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:43662638 G>A did not map to a codon.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr5:71495627 C>A maps to NM_005909.3 S2149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:210557732 T>A maps to NM_002374.3 L280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr19:40721090 G>A maps to NM_002446.3 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:40711136 C>T maps to NM_002446.3 H374H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr23:19398276 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr6:161470948 C>T maps to NM_005922.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr6:136963668 G>T maps to NM_005923.3 V609V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr19:39100634 G>A maps to NM_001042600.1 R281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:39104933 T>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:36638985 C>T maps to NM_018067.3 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr23:135318412 C>T did not map to a codon.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr4:156273879 C>T maps to NM_001039580.1 W563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:50691883 G>A maps to NM_002969.3 S350S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:144803782 C>T maps to NM_139021.2 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:30129060 C>T maps to NM_002746.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:19286474 C>T maps to NM_139034.2 S794S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr16:1814327 G>C maps to NM_015133.3 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr5:179674412 G>A maps to NM_001135044.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BV-01A-11D-A37C-09 chr15:42106768 G>A maps to NM_001128608.1 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr17:44067383 C>T maps to NM_001123066.3 Y441Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LW-01A-21D-A21Q-09 chr2:217234773 G>A maps to NM_020814.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr2:119739777 A>G maps to NM_006770.3 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:119750715 C>T maps to NM_006770.3 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:63667575 C>T maps to NM_001039469.2 N254N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr6:29455532 G>A maps to NM_052967.1 G49G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:18257755 C>T maps to NM_015016.1 A1047A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr5:66429428 C>T maps to NM_001164664.1 Y727Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr19:3778348 G>A maps to NM_002378.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr2:20205562 G>A maps to NM_002381.4 Y244Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I3-01A-11D-A38Z-09 chr20:43926657 G>A maps to ENST00000372754 R534R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:49279024 G>A maps to ENST00000389496 F387F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr20:54824447 G>A maps to ENST00000371389 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr5:112389544 C>T maps to NM_001085377.1 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U7-01A-11D-A29N-09 chr3:182789075 T>A maps to NM_020166.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:138678841 C>T did not map to a codon.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr23:138678808 G>T did not map to a codon.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr23:138701797 G>A did not map to a codon.
Sequencing variant TCGA-DX-A7EN-01A-11D-A38Z-09 chr3:182994709 C>T maps to NM_015078.2 G604G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr1:150551643 C>A maps to NM_021960.4 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr21:47704036 G>A maps to NM_003906.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr21:47662714 C>T did not map to a codon.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr22:35804412 G>A maps to NM_006739.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr5:94259672 A>G maps to NM_024717.4 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr5:94224611 C>T maps to NM_024717.4 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UA-01A-12D-A307-09 chr14:47324253 A>C maps to NM_001113498.2 V952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:47324286 C>T maps to NM_001113498.2 G941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr12:69210611 G>A maps to NM_002392.3 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A3OV-01A-11D-A228-09 chr6:90513120 T>C maps to NM_014611.1 Q85Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr14:24683306 G>A maps to NM_138476.3 Q152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPF-01A-11D-A38Z-09 chr11:86160929 C>T did not map to a codon.
Sequencing variant TCGA-JV-A5VF-01A-11D-A29N-09 chr23:70339253 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr3:151083704 C>T maps to NM_053002.4 L1050L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr3:151107921 A>G maps to NM_053002.4 P1834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr12:116408417 A>G maps to NM_015335.4 D2016D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr23:40511074 G>A did not map to a codon.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr23:40573853 C>T did not map to a codon.
Sequencing variant TCGA-MB-A8JL-01A-11D-A36J-09 chr19:871224 C>T maps to NM_005481.2 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr5:88025138 G>T maps to NM_002397.4 S287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UC-01A-11D-A307-09 chr16:3299598 C>T maps to NM_000243.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N1-A6IA-01A-12D-A32I-09 chr16:3298967 G>A maps to NM_000243.2 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HZ-01A-11D-A38Z-09 chr5:126774170 G>A maps to NM_032446.2 T715T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr1:3418450 C>A maps to ENST00000452816 S816S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr1:3425215 C>T maps to ENST00000452816 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr22:42154405 G>T maps to NM_152513.3 L663L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr22:42166716 C>T maps to NM_152513.3 L766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr6:46766859 G>A maps to NM_005588.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr2:112722786 C>T maps to NM_006343.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr7:116339236 C>T maps to NM_001127500.1 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr12:58163395 G>A maps to ENST00000408972 I200I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr12:58163563 G>C maps to ENST00000408972 Y175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48U-01A-11D-A307-09 chr17:60503813 C>T maps to NM_181725.3 N119N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:1555362 G>A maps to NM_001174118.1 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:44102102 C>T maps to NM_005926.2 K299K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:153433059 G>A maps to NM_005927.4 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:179107851 G>T maps to NM_033540.2 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:179107858 G>T maps to NM_033540.2 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:179069739 A>T maps to NM_033540.2 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2J-01A-11D-A387-09 chr12:53647128 C>G maps to NM_001170790.1 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:103343433 C>T did not map to a codon.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr15:41988902 A>T maps to ENST00000219905 I565I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr15:41989179 G>T maps to ENST00000219905 E658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:141705365 G>A maps to ENST00000475668 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr17:74944890 C>T maps to NM_198955.1 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr10:103558658 T>C maps to NM_012215.3 Q583Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr19:41281483 T>C maps to NM_006533.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr11:12231104 C>T maps to NM_014632.2 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr22:18273497 T>C maps to NM_015241.2 *2003W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:10535287 G>A did not map to a codon.
Sequencing variant TCGA-DX-A7EQ-01A-11D-A387-09 chr19:306712 T>A did not map to a codon.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr10:129901118 G>C maps to NM_002417.4 P2995P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr19:2041985 G>A maps to NM_199054.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:50506972 C>T maps to NM_015166.3 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:121131955 C>T maps to NM_014730.2 Q100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:118348797 C>T maps to NM_001197104.1 R1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr11:118376881 G>A maps to NM_001197104.1 A3425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:49426708 G>A maps to NM_003482.3 Q3927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB30-01A-11D-A38Z-09 chr7:151962268 C>T maps to ENST00000355193 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:36214020 C>A maps to NM_014727.1 P949P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:36228050 C>T maps to NM_014727.1 L2479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:104714102 C>A maps to NM_182931.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:104714101 C>T maps to NM_182931.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:2258588 G>A maps to NM_022372.4 S279S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:122617971 C>T maps to NM_014938.3 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr4:146575180 G>T maps to NM_172250.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr17:53488775 G>A maps to NM_012329.2 F37F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2J-01A-11D-A387-09 chr23:135047287 A>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:58079136 G>A maps to NM_002428.2 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr20:33851606 C>T maps to NM_006690.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr16:3100109 C>T maps to NM_022468.4 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr11:5012727 T>C did not map to a codon.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr11:102575383 A>G maps to NM_022122.2 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr11:102567417 G>T maps to NM_022122.2 I256I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:102567513 G>A maps to NM_022122.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KU-01A-32D-A24N-09 chr11:102714171 C>A did not map to a codon.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr11:102713512 G>A maps to NM_002422.3 D80D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:90857533 C>T maps to NM_007351.2 S901S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr10:88717175 C>T maps to NM_024756.2 W41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr22:28194944 C>T maps to NM_002430.2 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr14:61285543 G>A maps to NM_002431.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr1:158813135 T>G maps to NM_002432.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HZ-01A-11D-A38Z-09 chr3:49967151 G>A maps to NM_032355.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:108778672 C>T maps to NM_014429.3 K337K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:108836855 G>A maps to NM_014429.3 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I3-01A-11D-A38Z-09 chr23:14933789 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:100212793 C>T maps to NM_023948.4 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr6:132619015 C>T maps to NM_015529.2 W529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr9:13223586 C>T maps to ENST00000319217 E172E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr9:13217182 T>C maps to ENST00000319217 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr9:13175820 G>A maps to ENST00000319217 V995V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:58978336 G>A maps to NM_001039396.1 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:71360031 C>T maps to NM_005791.2 Q32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2G-01A-11D-A38Z-09 chr17:56348016 C>A maps to ENST00000340482 *778Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr22:43831029 A>C maps to NM_001044370.1 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr22:43831085 C>T maps to NM_001044370.1 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr1:167745357 C>T maps to NM_003953.5 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:60743897 G>A maps to NM_006039.3 W259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr11:18956292 T>G maps to NM_147199.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr11:18159468 C>G maps to NM_054031.3 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr11:18159000 G>A maps to NM_054031.3 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr19:10370386 A>T maps to NM_146387.1 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I3-01A-11D-A38Z-09 chr2:95753146 T>A maps to NM_031902.3 G416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:17997808 C>T maps to NM_001105569.1 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr5:80064659 G>A maps to NM_002439.3 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr5:79968151 A>T maps to NM_002439.3 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr1:76276462 T>C maps to NM_002440.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr6:31721191 C>T maps to ENST00000375742 L326L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr17:55704588 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr16:816490 G>C did not map to a codon.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr16:822907 G>T maps to NM_001025190.1 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:49934059 G>A maps to NM_002447.2 S784S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:190924814 G>A maps to NM_005259.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr5:174156456 C>A maps to NM_002449.4 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr16:56643193 T>C maps to NM_005953.3 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:242039045 G>A maps to NM_182501.3 V95V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:107371874 T>C maps to NM_025198.3 K206K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42W-01A-11D-A24N-09 chr15:31267167 A>G maps to NM_017762.2 D99D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EO-01A-11D-A36J-09 chr15:31217364 G>A maps to NM_014967.4 P736P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr22:30387565 A>T maps to NM_021090.3 K123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr17:56573690 T>C maps to NM_004687.4 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:17206509 C>T maps to NM_004686.4 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr23:63563502 A>C did not map to a codon.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr10:30602632 C>A maps to ENST00000358107 E682*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr4:100521751 T>G maps to ENST00000511045 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr4:100543869 C>A maps to ENST00000511045 G877G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr13:29600061 G>A maps to NM_001033602.2 Q419Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr13:29675027 C>G maps to NM_001033602.2 V865V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:30062138 C>T maps to NM_001033602.2 Q1178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr19:9080535 C>A maps to NM_024690.2 V3165V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:9066682 G>T maps to NM_024690.2 S6921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr19:9033270 G>A maps to NM_024690.2 L12119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr19:9033259 G>A maps to NM_024690.2 L12122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:9050055 G>A maps to NM_024690.2 I10525I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr19:9071241 T>A maps to NM_024690.2 R5402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:9070714 C>T maps to NM_024690.2 Q5577Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:9060451 G>A maps to NM_024690.2 S8998S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:9076120 C>T maps to NM_024690.2 Q3775Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:9076248 G>A maps to NM_024690.2 L3733L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr19:9076288 A>T maps to NM_024690.2 T3719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr19:9062572 G>A maps to NM_024690.2 S8291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr7:100678113 T>C maps to NM_001040105.1 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr7:100680099 G>A maps to NM_001040105.1 S1801S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr11:1098694 C>T maps to ENST00000441003 C2355C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:1104067 G>A maps to ENST00000441003 L2753L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DN-01A-12D-A27P-09 chr11:1085814 G>T maps to ENST00000441003 T912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr6:30954827 A>C maps to NM_001010909.2 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr11:1280227 G>T maps to ENST00000447027 G5553G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr11:1266536 G>T maps to ENST00000447027 L2812L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:1264736 G>A maps to ENST00000447027 T2212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr11:1267346 C>A maps to ENST00000447027 T3082T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42W-01A-11D-A24N-09 chr11:1031024 G>T maps to NM_005961.2 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:1369298 C>T maps to NM_032853.3 G487G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr23:105450723 G>T did not map to a codon.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr23:105450549 C>T did not map to a codon.
Sequencing variant TCGA-WK-A8XQ-01A-11D-A37C-09 chr23:105451168 T>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:103348405 G>A maps to NM_001018116.1 K256K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr9:103348639 C>T maps to NM_001018116.1 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr11:65633284 C>T maps to NM_025128.4 L503L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-QC-A7B5-01A-11D-A33E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:113530213 G>A maps to ENST00000189978 E351E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr21:42808960 G>T maps to NM_001144925.1 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr21:42807951 C>G maps to NM_001144925.1 G98G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EI-01A-11D-A33E-09 chr5:176734830 G>A maps to ENST00000423571 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EI-01A-11D-A33E-09 chr23:3236005 C>G did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:3241340 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr23:3235786 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr23:3242792 G>A did not map to a codon.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr23:3238223 T>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:50947028 G>A maps to NM_004533.3 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr19:50949208 G>A maps to NM_004533.3 K402K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr11:47364234 G>A maps to ENST00000399249 D506D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:47360231 T>C did not map to a codon.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr1:203144808 G>A maps to NM_004997.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr13:77799596 G>A maps to NM_015057.4 Q944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr13:77798599 T>C maps to NM_015057.4 G975G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:40366680 G>A maps to NM_001033082.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EQ-01A-11D-A387-09 chr12:81111288 G>A maps to NM_005593.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:81111150 C>T maps to NM_005593.2 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr17:10411235 A>T maps to NM_005963.3 G645G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-QQ-A5VC-01A-31D-A32I-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr17:10216010 G>A maps to NM_003802.2 C1415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr17:10225009 C>A maps to NM_003802.2 E984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr17:10267835 G>A maps to NM_003802.2 D4D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:50795621 G>A maps to NM_001145809.1 E1744E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr19:50813025 C>A maps to NM_001145809.1 S2030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:50735283 G>A maps to NM_001145809.1 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr17:10432928 G>C maps to NM_017534.5 V1023V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:10432354 C>T maps to NM_017534.5 R1132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr17:10436720 A>G maps to NM_017534.5 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr17:10533631 C>T maps to NM_002470.2 K1810K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr17:10541138 C>T maps to NM_002470.2 L1281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JK-01A-11D-A36J-09 chr17:10541188 C>A maps to NM_002470.2 E1265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr17:10533414 C>T maps to NM_002470.2 T1852T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:10363546 G>A maps to NM_017533.2 F413F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr14:23898536 G>T maps to NM_000257.2 Y386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr14:23900811 G>A maps to NM_000257.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr14:23899002 C>T maps to NM_000257.2 A373A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr17:10303853 C>T maps to NM_002472.2 R1196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr17:10309386 C>T maps to NM_002472.2 R801R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr22:36689834 G>A maps to NM_002473.4 S1304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr22:36737436 G>A maps to NM_002473.4 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr22:36678785 T>C maps to NM_002473.4 K1937K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:46781685 G>A maps to NM_182493.2 F140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:30387801 C>A maps to NM_013292.3 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr17:18023163 C>T maps to ENST00000205890 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr17:18025156 G>T maps to ENST00000205890 E1015*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HL-01A-11D-A387-09 chr13:109438080 G>A maps to NM_015011.1 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr13:109858994 G>T maps to NM_015011.1 V1796V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:109792909 G>A maps to NM_015011.1 G1428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:109535435 G>A maps to NM_015011.1 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KU-01A-32D-A24N-09 chr22:26176053 C>T maps to ENST00000407587 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2P-01A-11D-A387-09 chr22:26286799 G>A maps to ENST00000407587 R1466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A3OV-01A-11D-A228-09 chr22:26159313 G>A maps to ENST00000407587 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr22:26164342 T>C maps to ENST00000407587 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr22:26239727 C>T maps to ENST00000407587 Q1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QT-01A-12D-A32I-09 chr12:57441189 C>T maps to NM_005379.2 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:8601414 G>A maps to NM_012335.3 A622A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:8586452 G>A maps to NM_012335.3 Q1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:171256744 G>A maps to NM_138995.3 G613G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:171258030 G>A maps to NM_138995.3 E653E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:171319907 G>T maps to NM_138995.3 E921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr18:47431167 C>T maps to NM_001080467.2 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr18:47500967 T>C maps to NM_001080467.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr15:52571802 C>T maps to NM_018728.3 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:52567794 C>T maps to NM_018728.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr6:76617357 T>C maps to ENST00000428345 G1081G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:76893563 C>T maps to NM_000260.3 I1068I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr11:76918447 G>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr17:12656029 C>T maps to NM_001146312.1 F475F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:12626275 G>A maps to NM_001146312.1 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:203054909 G>A maps to NM_002479.4 H60H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr8:2044183 C>A maps to NM_003970.2 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr8:2024314 G>A maps to NM_003970.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr8:2037928 T>C maps to NM_003970.2 Y581Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:24432455 G>A maps to ENST00000330966 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr1:24400759 C>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:40275399 C>G maps to NM_015460.2 V652V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr3:40192544 G>T maps to NM_015460.2 L113L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr17:47869336 A>C maps to NM_007067.4 T35T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr10:76735645 C>G maps to NM_012330.2 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr20:62839307 C>A maps to NM_004535.2 G253G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr2:1947093 A>T maps to ENST00000399161 C55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr21:30248727 G>A maps to NM_013240.3 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr11:89924821 C>T maps to NM_005467.3 N710N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:13247127 C>T maps to NM_052876.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr9:138903667 G>A maps to NM_144653.3 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr1:1684500 T>A did not map to a codon.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr11:71194033 G>T maps to NM_018161.4 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr11:71164371 C>T maps to NM_018161.4 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr13:101717808 G>A maps to NM_052867.2 Y1517Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr23:92928274 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:48018104 G>A maps to NM_003827.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:47996380 G>A maps to NM_003827.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr15:60741045 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr8:18079882 C>T maps to NM_001160176.1 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr11:34156834 C>T maps to NM_024662.2 S675S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:3526269 C>T maps to NM_024845.2 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:201777650 G>A maps to ENST00000367296 K1317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:20072840 G>C maps to ENST00000396087 P1504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr11:20070456 C>A maps to ENST00000396087 L1385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:20065564 C>T maps to ENST00000396087 S1005S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr13:36223859 G>A maps to ENST00000400445 K2592K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr2:203972518 G>T maps to NM_001114132.1 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr2:203942511 T>G maps to NM_001114132.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr1:16907297 C>T maps to NM_017940.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr8:102731521 T>C maps to NM_032041.2 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:6636084 C>T maps to NM_014865.3 F921F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:158486168 G>A maps to NM_017760.5 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr7:74197916 C>T maps to NM_000265.4 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr22:37273720 G>A maps to NM_000631.4 G292G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5YA-01A-11D-A29N-09 chr2:133554263 A>G maps to NM_207363.2 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2J-01A-11D-A387-09 chr2:24985626 A>C maps to NM_003743.4 T1379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr20:46279838 G>A maps to NM_181659.2 Q1255Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr17:16004982 C>T maps to ENST00000395857 T773T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:55420787 G>A maps to NM_004829.5 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr19:55420622 C>A maps to NM_004829.5 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:160326886 C>T maps to NM_015331.2 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr8:134266811 C>T maps to NM_006096.3 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr5:149901310 C>T maps to NM_001543.4 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr4:115792053 A>T maps to NM_022569.1 L530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr4:115749049 C>A maps to NM_022569.1 V847V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:115856465 A>G maps to NM_022569.1 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr7:140402734 C>T maps to NM_004546.2 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr11:67378982 G>A maps to NM_007103.3 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr2:152463200 G>A maps to NM_001164507.1 D4222D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr2:152425137 G>A maps to NM_001164507.1 L5876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:152477456 C>T maps to NM_001164507.1 K3512K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr2:152582032 T>G maps to NM_001164507.1 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr2:152521903 G>A maps to NM_001164507.1 Y1727Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr2:152426885 A>G maps to NM_001164507.1 H5713H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr2:152512816 G>T maps to NM_001164507.1 T2115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MO-A47R-01A-11D-A24N-09 chr2:152581368 A>C did not map to a codon.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr2:152521284 G>A maps to NM_001164507.1 I1777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:152521284 G>A maps to NM_001164507.1 I1777I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:152512420 G>A maps to NM_001164507.1 Y2204Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr2:152527712 A>G maps to NM_001164507.1 L1444L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr10:21129757 C>T maps to ENST00000430741 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:11185839 C>T maps to NM_006403.3 W687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr22:29885938 G>A maps to NM_021076.3 A770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr8:24774754 G>T maps to NM_005382.2 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr4:170482981 C>T did not map to a codon.
Sequencing variant TCGA-K1-A42W-01A-11D-A24N-09 chr3:27393954 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:127088703 G>A maps to NM_001166171.1 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr11:20939732 C>T maps to NM_006157.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:212617711 C>T maps to NM_013349.4 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KU-01A-32D-A24N-09 chr18:70450952 T>A maps to NM_153181.2 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:74716820 C>T maps to NM_006656.5 Q224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr2:242756291 G>A maps to NM_001167599.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A850-01A-11D-A351-09 chr2:242755770 G>T maps to NM_001167599.1 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:182543167 G>A maps to NM_002500.2 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr12:55420484 C>T maps to NM_021191.2 R88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:29588839 C>T maps to NM_001042492.2 N1563N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr17:29576110 C>T maps to NM_001042492.2 R1362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr22:30032859 A>T maps to NM_181832.2 K79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr22:30032849 C>T maps to NM_181832.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr18:77170841 C>T maps to NM_172387.1 Y176Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:145659073 G>A maps to NM_013432.4 L1152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X2-A95T-01A-11D-A37C-09 chr8:145660402 G>A maps to NM_013432.4 D1001D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr11:129739601 G>A maps to NM_006165.3 T1131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr10:115661628 C>T maps to NM_198514.3 H448H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:17739679 C>T did not map to a codon.
Sequencing variant TCGA-MB-A5Y8-01A-11D-A29N-09 chr23:17742526 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr23:71359469 C>G did not map to a codon.
Sequencing variant TCGA-JV-A5VE-01A-11D-A29N-09 chr23:71359450 A>T did not map to a codon.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr1:236142370 C>T maps to NM_002508.2 K1182K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr20:25457262 C>T maps to NM_025176.4 T888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr4:48038017 A>G maps to NM_207330.1 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AK-01A-21D-A24N-09 chr1:24776052 C>T maps to NM_020448.4 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr1:24779929 C>T maps to NM_020448.4 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J0-01A-11D-A21Q-09 chr6:124979411 G>A maps to NM_001040214.1 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr16:50666203 C>T maps to NM_033119.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr5:172661846 G>T maps to NM_004387.3 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr3:173997209 G>A maps to NM_014932.2 A473A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K8-01A-11D-A21Q-09 chr3:173322870 G>T maps to NM_014932.2 P161P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr17:7320562 C>A maps to NM_020795.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr23:70389118 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:70387096 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr23:6069225 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:5810946 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr24:16952664 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr2:32449834 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BK-01A-11D-A37C-09 chr17:5436696 C>T maps to NM_033004.3 A1020A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr11:7981532 C>T maps to NM_176821.3 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr19:56329268 C>T did not map to a codon.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr19:54327233 C>A maps to ENST00000391773 G65G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JL-01A-11D-A36J-09 chr19:56416318 T>C maps to NM_176810.2 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:56443431 C>T maps to NM_176810.2 W82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr11:7059831 A>G maps to NM_176822.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:55481484 C>T maps to NM_017852.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr19:55494499 C>T maps to NM_017852.3 S478S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:55501974 G>A maps to NM_017852.3 G881G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:247587614 C>T maps to NM_004895.4 I290I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr19:56369583 G>T maps to NM_134444.4 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr19:56369982 G>A maps to NM_134444.4 W408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:56392905 C>T maps to NM_134444.4 L980L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr19:56539566 C>T maps to NM_153447.4 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:55450637 G>A maps to ENST00000446217 Q545*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:119043612 C>T maps to NM_024618.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr3:160960404 A>T maps to ENST00000472947 I327I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:169272384 G>A maps to NM_013330.3 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2P-01A-11D-A387-09 chr5:43702777 A>G maps to NM_182977.2 Q1017Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr16:69783470 C>T maps to NM_014062.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr7:144096230 G>A maps to ENST00000467773 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr12:132632203 T>A maps to NM_024078.1 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:30490911 G>A maps to NM_006092.2 A707A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:6586797 G>T maps to NM_024654.4 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V2-01A-11D-A32I-09 chr1:6585913 T>C maps to NM_024654.4 *703W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:6675464 C>T maps to ENST00000382421 K92K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:117723053 C>T maps to ENST00000338101 G458G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr12:117710225 G>A maps to ENST00000338101 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr17:26107794 G>A maps to NM_000625.4 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr7:150696415 G>A maps to NM_000603.4 R365R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr9:139407471 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr9:139417640 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr19:15285084 G>A maps to NM_000435.2 R1510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr19:15271748 G>T maps to NM_000435.2 P2230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr19:15276876 A>G maps to NM_000435.2 A1796A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr17:79916828 C>T maps to NM_178493.5 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:100104374 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:89177368 G>A maps to NM_016931.3 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr14:34263251 T>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:34269006 C>T maps to NM_001164749.1 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr1:5924039 G>T maps to NM_015102.2 I1350I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr19:36330256 G>T maps to NM_004646.3 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr19:36322587 G>A maps to NM_004646.3 V1081V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr22:39222585 G>A maps to NM_014293.2 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr4:156135354 C>T maps to NM_000910.2 F88F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr23:30326645 G>A did not map to a codon.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr23:30326653 T>C did not map to a codon.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr12:100926315 C>T maps to ENST00000392986 R176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:100934549 T>G maps to ENST00000392986 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:119530563 G>A maps to NM_022002.2 K209K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr12:95422247 T>C maps to NM_003297.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr4:149356398 C>T maps to ENST00000511528 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr10:115423584 G>T maps to ENST00000369358 I19I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr7:129367101 C>G maps to ENST00000393231 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr5:139251346 G>A maps to NM_013982.2 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr10:84744598 C>A maps to ENST00000404547 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:83635332 G>A maps to ENST00000404547 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr23:105153296 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:33474610 C>A maps to NM_003873.5 G792G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr10:33510662 G>A maps to NM_003873.5 Y422Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BN-01A-11D-A37C-09 chr2:206588536 G>T maps to NM_201266.1 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr5:176638414 C>T maps to NM_022455.4 L1005L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:176721766 G>A maps to NM_022455.4 K2466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr8:59548024 A>G did not map to a codon.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr8:59499074 G>A maps to NM_001144772.1 T827T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr2:18767588 T>C maps to ENST00000455492 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr12:104181306 T>G did not map to a codon.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr12:96180806 G>A maps to NM_021229.3 S165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr1:156837904 G>A maps to NM_002529.3 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr9:87563474 C>A maps to NM_006180.3 G621G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr23:51076292 C>T did not map to a codon.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr23:51075933 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr3:131101008 C>A maps to NM_152395.2 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:154042843 C>T maps to NM_207308.2 W820*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr4:77038822 G>A maps to ENST00000458189 I464I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr17:73228048 T>A maps to NM_024844.3 C457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr19:16918667 C>T maps to ENST00000438489 I1336I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr19:16860068 A>C maps to ENST00000438489 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:62568889 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:62568586 G>A maps to NM_006362.4 I295I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr17:708473 G>A maps to NM_022463.3 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr17:47656468 C>A maps to ENST00000513748 S189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EO-01A-11D-A36J-09 chr23:108781278 T>A did not map to a codon.
Sequencing variant TCGA-DX-A7EO-01A-11D-A36J-09 chr12:113425105 C>T maps to NM_016817.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr12:56618714 G>A maps to NM_024068.3 E25E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr1:228466603 C>T maps to NM_001098623.1 T2358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr1:228463524 C>G maps to NM_001098623.1 T2006T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr1:228521395 C>T maps to NM_001098623.1 V5323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ER-01A-11D-A36J-09 chr1:228494136 C>A maps to NM_001098623.1 T3908T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:228476584 G>A maps to NM_001098623.1 V3445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:228506747 C>T maps to NM_001098623.1 D4765D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-MB-A8JK-01A-11D-A36J-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:228404936 C>T maps to NM_001098623.1 T867T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:228466450 T>G maps to NM_001098623.1 G2307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr1:228451850 G>A maps to NM_001098623.1 A1540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:48834667 G>A maps to NM_001168254.1 E14E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr7:97616380 T>G maps to NM_006188.3 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:123630961 A>G did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:123637444 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:123526041 T>C did not map to a codon.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr23:123518623 A>T did not map to a codon.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr23:123780639 T>A did not map to a codon.
Sequencing variant TCGA-IE-A4EH-01A-11D-A24N-09 chr23:124097513 C>G did not map to a codon.
Sequencing variant TCGA-IE-A4EH-01A-11D-A24N-09 chr23:124097496 G>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:123699272 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr5:167654984 C>T maps to NM_001122679.1 S1781S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr5:167642245 G>A maps to NM_001122679.1 K1340K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr5:167552020 C>T maps to NM_001122679.1 C725C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A850-01A-11D-A351-09 chr5:167622270 C>T maps to NM_001122679.1 Y948Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr4:183268044 A>G maps to NM_001080477.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EK-01A-11D-A24N-09 chr4:183267831 A>T maps to NM_001080477.1 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr11:78497987 T>A maps to NM_001098816.2 K774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:78387280 G>A maps to NM_001098816.2 I1804I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr11:78383116 G>A maps to NM_001098816.2 F1918F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr23:13771530 G>C did not map to a codon.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr10:50953841 A>G did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:50944094 G>A maps to NM_018245.2 T961T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:50944181 C>T maps to NM_018245.2 E932E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:70787568 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:70775129 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:70787567 C>T did not map to a codon.
Sequencing variant TCGA-RN-A68Q-01A-11D-A307-09 chr19:9965242 G>A maps to NM_058164.2 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr13:53624758 G>A maps to NM_006418.3 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:29622770 G>A maps to NM_002544.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr11:76814247 C>T maps to NM_006189.1 D121D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr3:193372785 T>A maps to NM_130837.2 T716T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr10:98109508 T>G maps to NM_033207.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:132306559 C>A maps to NM_002545.3 E260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr23:67283812 C>A did not map to a codon.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr8:145110769 G>A maps to ENST00000360660 A723A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M4-01A-11D-A21Q-09 chr8:145111872 G>A maps to ENST00000360660 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23V-01A-11D-A29N-09 chr23:153492788 G>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:88419678 G>A maps to NM_001030015.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:88419684 T>C maps to NM_001030015.2 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr10:88418323 C>T maps to NM_001030015.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr8:54163588 G>A maps to NM_000912.3 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EK-01A-11D-A24N-09 chr1:203468846 A>G maps to NM_014359.3 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:48596331 C>T maps to NM_001004134.1 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr1:159283693 G>A maps to NM_001004467.1 H252H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5YA-01A-11D-A29N-09 chr1:159504981 A>T maps to NM_001004469.1 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr1:158435374 G>A maps to NM_001004473.1 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:158435386 C>T maps to NM_001004473.1 F12F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:158369022 G>A maps to NM_001004475.1 I78I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:158548921 G>A maps to NM_001004477.1 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr1:158577163 A>G maps to NM_001004478.1 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr6:29395184 T>A maps to NM_013937.2 A78A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:16449126 G>A maps to NM_001005239.1 F226F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr14:20711360 C>T maps to NM_001004479.1 C137C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:20692108 C>T maps to NM_001004480.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr6:29365078 G>T maps to NM_013936.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr6:29365078 G>T maps to NM_013936.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr6:29342524 C>T maps to NM_030959.2 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr9:107298239 G>T maps to NM_001001961.1 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr9:107288553 T>G maps to NM_001001919.1 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr9:107360877 A>G maps to NM_001004482.1 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr9:107331951 C>T maps to NM_001004483.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr9:107457046 T>A maps to NM_001004484.1 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr9:107456941 C>A maps to NM_001004484.1 I80I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QU-01A-11D-A27P-09 chr1:247835650 C>T maps to NM_001005487.1 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YU-01A-12D-A33E-09 chr17:2996237 G>T maps to NM_002548.2 S18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB35-01A-21D-A417-09 chr16:3254695 G>T maps to NM_012360.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:125273337 G>A maps to ENST00000444856 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X2-A95T-01A-11D-A37C-09 chr11:57982689 A>T maps to NM_001004458.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VF-01A-11D-A29N-09 chr11:57970681 G>C maps to NM_001004459.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:143826480 C>T maps to NM_001001659.1 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr7:143826691 C>T maps to NM_001001659.1 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:6807179 C>T maps to NM_001004489.2 V304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr6:29054539 C>T maps to NM_001005226.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr7:143658016 A>G maps to NM_012369.2 *318W. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr7:143633089 G>A maps to NM_001004685.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr6:29141720 C>T maps to NM_030905.2 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:248202180 C>T maps to NM_001004686.2 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:248224294 G>A maps to NM_001004687.1 S104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr1:248367160 T>C maps to NM_001004689.1 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr1:248308469 C>T maps to NM_001004690.1 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:248309348 A>C maps to NM_001004690.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:248487738 G>A maps to NM_001004691.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr1:248458734 C>T maps to NM_001004692.1 W49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr1:248637397 C>T maps to NM_001005495.1 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:248436693 C>T maps to NM_001004695.1 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr1:248737311 G>A maps to NM_001001821.1 H249H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr1:248525878 C>T maps to NM_001004696.1 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:248551772 C>T maps to NM_001005471.1 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr1:248084654 C>T maps to NM_001005522.1 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:180582382 G>A maps to NM_206880.1 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr5:180582646 G>A maps to NM_206880.1 W235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:8842040 C>T maps to NM_001004699.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr11:48510418 T>A maps to NM_001005512.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:49974639 C>T maps to NM_001001955.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3NK-01A-11D-A21Q-09 chr11:55322429 T>C maps to NM_001001920.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:55322123 C>T maps to NM_001001920.1 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr11:55340373 A>C maps to NM_001004701.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr11:48347058 T>G maps to NM_001004702.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:51516171 G>A maps to NM_001004703.1 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr11:59271503 C>A maps to NM_001004706.1 G152G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr11:123810991 C>T maps to NM_001001965.1 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr11:123810922 G>A maps to NM_001001965.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:59283137 C>T maps to NM_001004711.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr15:102346824 A>T maps to NM_001005326.1 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr14:20482731 A>T maps to NM_001004712.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr14:20443866 T>C maps to NM_001005486.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr14:20388806 G>T maps to NM_001005483.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ET-01A-11D-A36J-09 chr14:20249200 C>G maps to NM_001005500.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr15:22368625 A>G maps to NM_001004719.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr14:20296161 C>T maps to NM_001004723.1 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr11:48267305 G>C maps to NM_001004727.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:48266852 C>T maps to NM_001004727.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:4976385 G>A maps to NM_001004748.1 V186V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:4967670 G>A maps to NM_001005329.1 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:4929471 C>T maps to NM_001004749.1 Y291Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:5363995 C>T maps to NM_001005567.1 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr11:4842932 C>T maps to NM_001004753.1 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KU-01A-32D-A24N-09 chr11:4944761 G>A maps to NM_001005237.1 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J0-01A-11D-A21Q-09 chr11:5474865 C>T maps to NM_001004754.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr11:4869964 A>G maps to NM_001004758.1 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:5905836 T>C maps to NM_001005165.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:5878605 G>A maps to NM_001005168.1 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:4470781 C>T maps to NM_001005172.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2L-01A-32D-A417-09 chr11:6007449 G>A maps to NM_001005173.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr11:4566605 C>G maps to NM_001004137.1 Y62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:5842311 C>T maps to NM_001005174.1 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:5841993 C>T maps to NM_001005174.1 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A3PN-01A-11D-A228-09 chr11:6221370 A>G maps to NM_001005178.1 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BV-01A-11D-A37C-09 chr11:5969151 C>T maps to NM_001003443.2 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:5758027 C>T maps to NM_001005180.2 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr3:97806243 A>C maps to NM_054106.1 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr11:56757026 C>T maps to NM_001005323.1 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr11:55798715 G>T maps to NM_001001921.1 V274V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:55563414 C>T maps to NM_001004735.1 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr11:55761684 G>T maps to NM_003697.1 T139T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr3:97852059 A>T maps to NM_001005338.1 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:97851549 G>A maps to NM_001005338.1 E3E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr3:97868429 T>A maps to NM_001005514.1 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr11:55944512 G>A maps to NM_001005492.1 K140K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:55579025 C>T maps to NM_001004738.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr11:55579034 C>T maps to NM_001004738.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:56380051 G>A maps to NM_001004740.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:56310061 G>A maps to NM_001005245.1 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr11:7817739 G>T maps to NM_153444.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:56000262 G>A maps to NM_001004746.1 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:6816612 G>A maps to NM_003696.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:143701181 C>T maps to NM_001005281.1 F31F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:55846089 C>T maps to NM_054105.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2P-01A-11D-A387-09 chr12:55725939 C>A maps to NM_054104.1 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:55688131 C>T maps to NM_001005493.1 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr12:55759379 G>T maps to NM_001005497.1 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:55759634 C>T maps to NM_001005497.1 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:247875340 G>A maps to NM_001005286.1 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:247875799 C>T maps to NM_001005286.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr1:158725396 C>A maps to NM_001005184.1 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr1:158735722 G>A maps to NM_001005185.1 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr19:14939049 C>A maps to NM_017506.1 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr19:14910159 T>C maps to NM_198944.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:9325174 G>A maps to NM_001005191.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr19:9225932 G>T maps to ENST00000293614 C169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr19:9213640 C>T maps to NM_001005193.1 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr11:124413016 A>G maps to NM_001005195.1 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr11:124294277 G>A maps to NM_001005196.1 R164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr11:56057791 G>T maps to NM_001005199.1 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:55890477 C>T maps to NM_001005201.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr11:56113792 G>T maps to NM_001002907.1 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:55927454 G>A maps to NM_001004058.2 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr12:48920301 G>A maps to NM_001005203.2 K296K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:48919764 G>A maps to NM_001005203.2 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr11:56510852 C>T maps to NM_001005284.1 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr12:55524484 G>A maps to NM_001005243.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:57958888 G>A maps to NM_001005283.2 K309K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LW-01A-21D-A21Q-09 chr12:58112179 G>A maps to NM_006812.3 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr12:58113951 G>C maps to NM_006812.3 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr12:58111996 G>A maps to NM_006812.3 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr22:31266575 C>T maps to NM_030758.3 D338D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr7:24902872 C>T maps to NM_015550.2 S272S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:24903198 G>A maps to NM_015550.2 A231A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr11:3113682 G>T maps to NM_020896.3 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:179260225 C>T maps to ENST00000392505 T940T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr17:45891081 G>A maps to NM_145798.2 D490D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UD-01A-11D-A307-09 chr19:54598509 G>A maps to NM_130771.3 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr19:54598485 T>G maps to NM_130771.3 *268C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2F-01A-11D-A387-09 chr16:21702928 C>T maps to ENST00000286149 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HZ-01A-11D-A38Z-09 chr2:26750773 C>T maps to NM_194248.2 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr2:26698229 G>A maps to NM_194248.2 S1041S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr2:26698259 G>A maps to NM_194248.2 I1031I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr2:26687735 C>T did not map to a codon.
Sequencing variant TCGA-DX-A7EQ-01A-11D-A387-09 chr17:72927064 C>T maps to NM_178160.2 D445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr17:72937677 A>G maps to NM_178233.1 Q88Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:63764972 C>T maps to ENST00000422031 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr15:31819494 G>A maps to ENST00000382902 H223H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XQ-01A-11D-A37C-09 chr2:63283300 T>A maps to NM_014562.3 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:7723022 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr11:65562101 A>T maps to NM_004561.2 K138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BN-01A-11D-A37C-09 chr12:133197921 G>A maps to NM_170683.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:133196051 C>T maps to NM_170683.2 Y67Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr11:57135557 C>T maps to NM_002559.2 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:21380900 C>T maps to NM_005446.3 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:78216518 C>T did not map to a codon.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr23:69479069 C>T did not map to a codon.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr23:69479427 G>T did not map to a codon.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr11:73990431 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr11:47199922 G>A maps to NM_016223.4 R385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr1:17531792 G>A maps to NM_013358.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:17563877 G>A maps to NM_013358.2 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr1:17413051 G>T maps to NM_007365.2 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:17422424 C>T maps to NM_007365.2 V130V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:17607194 G>T maps to NM_016233.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:17593269 C>T maps to NM_016233.2 D155D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr1:17707594 C>A maps to NM_207421.3 C163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:42804232 G>A maps to NM_001145940.1 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr23:55248261 T>A did not map to a codon.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr23:55248255 G>A did not map to a codon.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr23:110390986 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:110366498 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:110366497 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr1:100154946 G>A maps to NM_017734.4 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2IZ-01A-11D-A21Q-09 chr12:56718436 C>T maps to NM_001127460.2 K552K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:93912978 C>T maps to NM_015368.3 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr10:135197626 G>A maps to NM_152911.2 E344E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr5:78944892 C>T maps to NM_173797.3 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr9:119065138 C>T maps to NM_002581.3 F1019F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr9:119130030 G>T maps to NM_002581.3 E1535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr1:176679191 A>G maps to NM_020318.2 V1177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr1:176526054 C>A maps to NM_020318.2 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr15:69682068 C>A maps to NM_017705.3 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr3:142681479 G>A maps to NM_198504.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:14702153 G>A maps to NM_002582.2 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr22:44395416 G>A maps to NM_001003828.1 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr22:44543774 C>T maps to NM_001003828.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr23:150840782 G>C did not map to a codon.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr23:150840062 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:150842500 C>T did not map to a codon.
Sequencing variant TCGA-SI-AA8C-01A-11D-A387-09 chr23:150789981 A>G did not map to a codon.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr2:242046864 G>A maps to ENST00000358649 R1246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr2:242054558 G>A maps to ENST00000358649 Q1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr2:242047681 C>A maps to ENST00000358649 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr2:242062176 C>T maps to ENST00000358649 W1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:21695440 G>A maps to NM_006192.3 *535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr7:127253882 C>A maps to NM_006193.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:127253566 A>G maps to NM_006193.2 Y186Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr7:127251687 C>A maps to NM_006193.2 E264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:127255453 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:52595908 G>A maps to ENST00000296302 L1388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:134071954 G>A maps to NM_032961.1 G220G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EN-01A-11D-A38Z-09 chr23:91642818 G>A did not map to a codon.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr24:4967351 G>T did not map to a codon.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr24:4925425 T>A did not map to a codon.
Sequencing variant TCGA-DX-A7ER-01A-11D-A36J-09 chr24:4925492 T>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr24:4925405 C>T did not map to a codon.
Sequencing variant TCGA-DX-A6B9-01A-12D-A32I-09 chr5:141334715 G>A maps to NM_016580.2 Q901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5Y8-01A-11D-A29N-09 chr10:56129014 G>A maps to NM_001142763.1 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr4:138452381 A>G maps to NM_019035.3 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr23:99662488 G>C did not map to a codon.
Sequencing variant TCGA-X9-A971-01A-11D-A387-09 chr13:61986223 G>A maps to NM_022843.3 R670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:67802371 A>T maps to NM_203487.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr5:140166037 G>T maps to NM_018900.2 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr5:140165937 C>T maps to NM_018900.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71O-01A-12D-A33E-09 chr5:140167899 G>A maps to NM_018900.2 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr5:140236982 C>T maps to NM_018901.2 N450N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140250307 C>T maps to NM_018902.3 G540G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140250272 C>T maps to NM_018902.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140250271 G>A maps to NM_018902.3 E528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr5:140257090 G>A maps to NM_018903.2 T678T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr5:140186933 G>A maps to NM_018907.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr5:140202745 C>T maps to NM_018908.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5Y9-01A-11D-A29N-09 chr5:140202721 C>T maps to NM_018908.2 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr5:140202595 G>A maps to NM_018908.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr5:140209097 C>T maps to NM_018909.2 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr5:140208761 C>T maps to NM_018909.2 D362D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr5:140208143 C>T maps to NM_018909.2 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr5:140214123 G>A maps to NM_018910.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr5:140221826 T>C maps to NM_018911.2 N307N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr5:140222279 C>T maps to NM_018911.2 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140229444 C>T maps to NM_031857.1 F455F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr5:140230347 G>A maps to NM_031857.1 Q756Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr5:140307700 C>A maps to NM_018898.3 I408I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr5:140348243 C>T maps to NM_018899.5 D631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr5:140431714 G>A maps to NM_013340.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140580723 C>T maps to NM_018931.2 F459F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140590362 G>A maps to NM_018932.3 R628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr5:140595647 G>T maps to NM_018933.2 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr5:140595443 C>A maps to NM_018933.2 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr5:140605260 C>T maps to NM_018934.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr5:140604756 C>T maps to NM_018934.2 F560F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr5:140626729 G>A maps to NM_018935.2 E528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr5:140475384 C>T maps to NM_018936.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr5:140476098 C>T maps to NM_018936.2 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr5:140481897 C>T maps to NM_018937.2 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr5:140503454 C>A maps to NM_018938.2 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr5:140503385 G>A maps to NM_018938.2 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140516692 C>T maps to NM_015669.2 F559F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr5:140531233 C>T maps to NM_018939.2 L466L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140531766 G>A maps to NM_018939.2 K643K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140554452 C>T maps to NM_018940.2 D679D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140554453 C>T maps to NM_018940.2 Q680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr5:140559084 G>A maps to NM_019120.2 S490S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BV-01A-11D-A37C-09 chr5:140710511 G>A maps to NM_018912.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140710481 G>A maps to NM_018912.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140794682 A>G maps to NM_018913.2 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr5:140720139 G>A maps to NM_018915.2 A534A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr5:140720409 C>T maps to NM_018915.2 G624G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr5:140724709 C>T maps to NM_018916.3 D370D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140773132 C>T maps to NM_032088.1 V251V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr5:140784396 G>A maps to NM_018921.2 V626V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr5:140769481 C>T maps to NM_003736.2 P677P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:140767510 C>T maps to NM_003736.2 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr11:82879707 C>T maps to NM_015885.3 S777S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr11:82880376 C>T maps to NM_015885.3 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:113845240 A>G maps to ENST00000246505 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr7:82581541 G>A maps to NM_033026.5 V2909V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr7:82585950 C>A maps to NM_033026.5 E1440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr7:82545960 G>A maps to NM_033026.5 R3781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr7:82544713 A>G maps to NM_033026.5 I4196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr7:82584754 C>T maps to NM_033026.5 P1838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:82545982 C>T maps to NM_033026.5 V3773V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr21:47848500 C>T maps to NM_006031.5 Q2563*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr21:47836527 G>A maps to NM_006031.5 K2232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:233134993 G>A maps to NM_014801.3 S1820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:65401772 C>T maps to NM_032223.2 S1549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:100202810 C>T maps to NM_002593.3 S187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr20:17339054 C>T maps to NM_002594.2 N122N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr19:1486914 G>A maps to NM_017573.3 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr2:70504005 G>T maps to NM_016297.3 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr2:70486510 T>C maps to NM_016297.3 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:105203054 C>T maps to NM_014976.1 L1697L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:34900199 C>T maps to NM_032346.1 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr2:178592478 C>T maps to NM_016953.3 W650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:57543203 G>A maps to NM_177966.5 E366E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr2:183095804 C>T maps to NM_005019.3 E173E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:183032973 T>G maps to NM_001003683.1 *536Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr7:31864524 G>A maps to NM_001191057.1 I454I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:31887592 C>T maps to NM_001191057.1 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:31877577 G>A maps to NM_001191057.1 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr1:66834586 C>A maps to NM_001037341.1 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr19:18327582 G>A maps to NM_000923.3 R485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:144931146 G>A maps to NM_001002811.1 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr4:120549676 G>A maps to NM_001083.3 T50T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:149247672 C>T maps to NM_000440.2 W728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr5:149245771 T>C maps to NM_000440.2 Q773Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr8:66701115 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:136508237 C>T maps to NM_018945.3 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr5:76709034 C>T maps to NM_003719.3 I604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr7:550607 C>T maps to NM_002607.5 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KU-01A-32D-A24N-09 chr16:335672 C>T maps to NM_006849.2 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr7:148705271 C>A maps to NM_004911.4 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr7:148701071 G>A maps to NM_004911.4 D584D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPF-01A-11D-A38Z-09 chr4:95506839 C>T maps to NM_006457.3 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:94934286 C>T maps to NM_001161778.1 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB30-01A-11D-A38Z-09 chr6:107475957 G>A maps to NM_020381.3 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr13:28498561 C>A maps to NM_000209.3 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:1961226 C>T maps to NM_024411.4 K169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr5:32089052 G>A maps to NM_178140.2 K1833K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:73433538 G>A maps to NM_015009.1 F726F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr12:41961622 C>T maps to NM_001164595.1 F502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr19:57333111 C>T maps to NM_006210.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr19:57327589 A>T maps to NM_006210.2 P740P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:57326182 C>T maps to NM_006210.2 R1209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr11:66243175 G>A maps to NM_145065.2 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr8:57353920 G>A maps to NM_001135690.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HZ-01A-11D-A38Z-09 chr2:239170423 G>C maps to NM_022817.2 A454A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr4:152600964 C>T maps to NM_004564.2 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr17:8167127 G>A maps to NM_012393.2 W555*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr23:54978377 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr21:45738391 G>T maps to NM_002626.4 E326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr21:45742860 C>T maps to NM_002626.4 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr12:48535749 C>T maps to NM_001166686.1 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:50724595 G>A maps to ENST00000515869 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr19:15580568 A>G maps to NM_052890.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr19:15586655 G>A maps to NM_052890.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:64104442 C>T maps to NM_002633.2 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr4:37831662 C>T maps to NM_018290.3 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr11:100996759 G>C maps to NM_000926.4 V589V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr1:33820032 C>G maps to ENST00000419414 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr3:169863249 C>T maps to NM_024947.3 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr23:22231039 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr23:22196423 T>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:133914742 G>A maps to ENST00000448712 K763K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr8:133851692 C>A maps to ENST00000395386 C752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr23:133527619 T>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:79707141 A>G maps to NM_017934.5 A730A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ET-01A-11D-A36J-09 chr23:71855040 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr23:71800879 A>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:71813107 A>T did not map to a codon.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr23:18959719 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:118499009 C>A maps to NM_015157.2 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:111632167 G>A maps to NM_001134438.1 E446E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr8:22079105 G>A maps to NM_014759.3 R251R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr22:21084216 G>A maps to NM_058004.2 P1399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr1:151288731 C>A maps to NM_002651.2 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr2:46842276 T>C maps to NM_002643.3 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr16:624229 G>A maps to NM_148920.1 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr1:207110638 G>A maps to NM_002644.3 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:44045317 C>T maps to NM_015937.4 Q117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr10:98363807 T>A did not map to a codon.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr10:98386534 T>A maps to NM_152309.2 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr11:17121489 A>G maps to NM_002645.2 L1345L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:204438495 C>T maps to NM_002646.3 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr3:138478101 G>C maps to NM_006219.1 G28G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U5-01A-11D-A228-09 chr1:9783347 G>A maps to ENST00000361110 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:67590974 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:8726793 G>A maps to NM_001010855.2 S512S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr2:209215654 C>A maps to NM_015040.3 A1865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr23:48771548 C>A did not map to a codon.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr23:48772491 G>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:48771445 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:48771444 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:9949264 C>A maps to NM_006221.2 S71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:71417245 C>T did not map to a codon.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr7:142829268 C>T maps to NM_002652.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2P-01A-11D-A387-09 chr11:67263035 C>T maps to NM_004910.2 E785E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr11:67261232 G>A maps to NM_004910.2 D1028D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr17:6381306 G>A maps to NM_031220.3 I296I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr17:6380416 C>T maps to NM_031220.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr8:22145079 G>A maps to NM_001135721.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr8:22138935 G>A maps to NM_001135721.1 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr16:2153896 C>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr7:47835733 G>C maps to NM_138295.3 L2736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr5:137226242 C>A maps to ENST00000230643 Y35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr22:46655313 G>A maps to NM_006071.1 N1302N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr6:51930780 G>C maps to NM_138694.3 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:51890773 G>A maps to NM_138694.3 F1278F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr6:51701241 G>A maps to NM_138694.3 V2711V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr6:51776644 C>A maps to NM_138694.3 E2148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr8:110456115 C>T maps to ENST00000426474 L1592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr8:110527529 C>T maps to ENST00000426474 Y3896Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr8:110453570 G>A maps to ENST00000426474 G1389G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr1:155265485 C>T maps to ENST00000423816 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5Y9-01A-11D-A29N-09 chr19:14581436 C>T maps to NM_213560.1 N835N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr12:32977077 G>A maps to NM_004572.3 G569G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr1:20474782 C>A maps to NM_022819.3 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr15:42448729 C>T maps to ENST00000397272 W6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr15:42444922 C>T maps to ENST00000397272 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:42437880 C>T did not map to a codon.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr1:20416374 C>T maps to NM_000929.2 G93G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:20416383 C>T maps to NM_000929.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:8722147 G>A maps to NM_015192.2 V817V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr15:40591137 C>T maps to NM_004573.2 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr20:9370584 C>T maps to NM_001172646.1 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr10:96022443 C>T maps to ENST00000371380 C1336C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr10:96012078 G>T maps to ENST00000371380 G1035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr10:96058262 C>A maps to ENST00000371380 A1765A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A3PN-01A-11D-A228-09 chr20:39792473 G>T did not map to a codon.
Sequencing variant TCGA-DX-A240-01A-32D-A27P-09 chr1:2411239 C>T maps to NM_014638.2 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:198949936 C>T maps to NM_006226.3 R566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr2:198948488 C>G maps to NM_006226.3 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr23:215828 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:18889210 A>G maps to ENST00000266505 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr8:144995432 G>A maps to NM_201380.2 G2989G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:144991327 G>A maps to NM_201380.2 Q4358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:144991328 G>A maps to NM_201380.2 D4357D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr8:38827159 C>T maps to NM_021623.1 F379F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr2:179365892 A>G maps to NM_019091.3 E255E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr12:45567095 C>G maps to ENST00000256692 V351V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L4-01A-12D-A26G-09 chr19:39911413 C>T maps to NM_022835.2 L441L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr16:67315958 C>G maps to NM_001129729.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:67318356 G>A maps to NM_001129729.1 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:6533331 G>A maps to NM_198681.2 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr17:43530772 C>T maps to NM_014798.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:43528022 C>T maps to NM_014798.2 P868P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr1:16054147 G>T maps to ENST00000420314 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr1:16045047 C>T maps to ENST00000420314 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:16057088 C>T maps to ENST00000420314 S860S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr1:150131552 G>T maps to ENST00000443480 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr9:19116353 T>C maps to NM_001122.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:4512774 C>T maps to NM_001080400.1 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr20:21142510 G>A did not map to a codon.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr4:128812804 C>T maps to NM_014264.4 N669N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:142403135 C>T maps to NM_001172312.1 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr23:114863596 A>T did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr20:44539884 G>A maps to NM_006227.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr17:37226189 G>A maps to NM_020405.4 V434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr3:126748377 C>T maps to NM_032242.3 Y1623Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr1:208390562 C>G maps to NM_025179.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:153692616 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5V2-01A-11D-A32I-09 chr23:153696279 C>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:131825506 C>T maps to NM_020911.1 K1763K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:132070005 G>A maps to NM_001105543.1 R474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr3:48465045 G>C maps to NM_001130082.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:48461036 G>A maps to NM_001130082.1 I886I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr22:50717057 C>T maps to NM_012401.2 R1538R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr22:50719042 G>A maps to NM_012401.2 F1350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:50717401 G>A maps to NM_012401.2 A1476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N1-A6IA-01A-12D-A32I-09 chr23:153044435 T>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VD-01A-42D-A38Z-09 chr23:153033836 G>T did not map to a codon.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr1:205811877 A>G maps to NM_152491.4 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr16:72166710 C>A maps to NM_031293.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr16:72162647 G>T maps to NM_031293.2 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr15:74290385 C>T maps to NM_033238.2 C57C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ET-01A-11D-A36J-09 chr17:15134332 C>T maps to NM_000304.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr7:102949430 G>A maps to NM_004279.2 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr6:160238166 C>T maps to NM_173516.1 L370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:118351373 G>A maps to NM_006229.2 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr14:74180000 C>T maps to NM_006029.4 W114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr23:152226126 G>C did not map to a codon.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr23:152159720 T>G did not map to a codon.
Sequencing variant TCGA-DX-A3UD-01A-11D-A307-09 chr22:44333048 G>A maps to NM_025225.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr22:44335889 A>T maps to NM_025225.2 K333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr23:7894059 T>G did not map to a codon.
Sequencing variant TCGA-DX-AB2J-01A-11D-A387-09 chr19:7622126 C>T maps to NM_001166111.1 D1128D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr9:140379045 G>A maps to NM_001098537.1 S780S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr9:140437932 T>A maps to NM_001098537.1 K153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr9:140409906 C>T maps to NM_001098537.1 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EH-01A-11D-A24N-09 chr7:131190688 G>A maps to NM_001018111.2 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr23:84560868 C>A did not map to a codon.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr23:84614562 G>C did not map to a codon.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr1:166810313 G>T maps to NM_017542.3 E41*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:113333218 C>T maps to NM_019014.4 I1107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr17:7414574 G>T maps to NM_000937.4 L1285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:621792 C>T maps to NM_005035.3 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr7:53103957 C>T maps to NM_182595.3 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr7:94992146 G>A maps to NM_000940.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EN-01A-11D-A38Z-09 chr23:48372970 G>T did not map to a codon.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr23:48374460 G>A did not map to a codon.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr23:48370297 C>T did not map to a codon.
Sequencing variant TCGA-DX-A2J4-01A-32D-A21Q-09 chr18:14542899 A>G maps to ENST00000444806 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr18:14537922 G>A maps to ENST00000444806 G229G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr18:14538211 T>A maps to ENST00000444806 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr21:14983025 C>T maps to NM_174981.3 V159V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr2:131976100 C>T maps to NM_001083538.1 N42N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VD-01A-42D-A38Z-09 chr2:132022030 C>T maps to NM_001083538.1 G1001G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr2:130877845 G>A maps to NM_001099771.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:130869581 C>T maps to NM_001099771.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr2:130832536 G>A maps to NM_001099771.2 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr14:20007610 G>A maps to ENST00000439503 D444D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J4-01A-32D-A21Q-09 chr3:87322590 C>A maps to NM_001122757.1 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C7-01A-11D-A36J-09 chr19:42626728 C>T did not map to a codon.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr1:38511692 C>T maps to NM_002699.3 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr6:99283813 G>A maps to NM_005604.2 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr4:147561227 G>A maps to NM_004575.2 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr4:147560579 G>A maps to NM_004575.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A8OO-01A-11D-A36J-09 chr5:145719325 C>T maps to NM_002700.2 H112H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr5:93076579 C>T maps to NM_153216.1 Q230Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr7:39247148 C>A maps to NM_007252.3 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr19:288082 G>T maps to NM_177543.1 Y68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr9:134183430 C>T maps to NM_032728.3 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23V-01A-11D-A29N-09 chr22:46594477 G>C maps to NM_001001928.2 S66S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BK-01A-11D-A37C-09 chr3:12458564 C>G maps to NM_015869.4 P394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:23803470 G>A maps to NM_013261.3 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr5:149216578 C>G maps to NM_133263.3 S854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:18725933 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:76808019 G>A maps to NM_006239.2 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:49649427 C>T maps to NM_003660.2 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr11:7669672 G>T maps to NM_003621.2 E568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr11:7669671 G>T maps to NM_003621.2 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:64452345 G>A maps to NM_000942.4 F100F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I3-01A-11D-A38Z-09 chr5:102486983 C>A maps to ENST00000451606 R312R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr2:44429141 G>A maps to NM_002706.4 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:202544233 C>T maps to ENST00000367270 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:202318210 C>T maps to ENST00000367270 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr1:202385934 G>A maps to ENST00000367270 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr14:104202498 C>T maps to NM_015316.2 A1024A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:49376798 C>T maps to NM_014330.3 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr1:204378835 A>G maps to NM_032833.3 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr10:93390508 G>A maps to NM_005398.4 Y43Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V2-01A-11D-A32I-09 chr23:49142964 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr17:48213001 G>A maps to NM_032595.3 F770F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X2-A95T-01A-11D-A37C-09 chr8:26218554 T>G maps to NM_001177591.1 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr5:146080607 C>T maps to ENST00000394414 E122E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:295210 G>A did not map to a codon.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr11:64695299 G>A maps to NM_006244.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr14:102359441 C>G maps to NM_002719.3 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr14:102359442 C>T maps to NM_002719.3 Q266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr6:42974818 G>T maps to NM_006245.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:104356750 C>T maps to NM_147180.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr19:46891838 G>A maps to NM_006247.2 V402V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:8563135 G>A maps to NM_032152.4 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:12954685 C>T maps to NM_001039361.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:12954571 G>A maps to NM_001039361.3 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:12888397 G>A maps to NM_001146344.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:12887196 G>A maps to NM_001146344.1 F220F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr1:13038326 G>T maps to NM_001100631.1 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr11:129785665 G>A maps to NM_020228.2 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr11:45203361 C>T maps to NM_020229.2 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr8:70981630 C>T maps to NM_024504.2 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr1:3329295 G>A maps to NM_022114.3 A845A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr1:3342726 G>T maps to NM_022114.3 S1074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr1:14106017 T>G maps to NM_012231.4 T576T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr16:90128854 A>T maps to NM_001098173.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:23526340 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr20:47274766 C>A did not map to a codon.
Sequencing variant TCGA-PC-A5DN-01A-12D-A27P-09 chr1:186277601 C>T maps to NM_005807.3 D917D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:186276983 G>A maps to NM_005807.3 G711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:186281400 G>A maps to NM_005807.3 T1296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr13:28562732 G>A maps to NM_001105577.1 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:62195065 G>A maps to NM_001037335.2 I1703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:64085356 G>A maps to NM_198859.3 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr5:40765099 C>T maps to NM_206907.3 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr9:71628288 G>A maps to NM_002732.3 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:71628255 G>A maps to NM_002732.3 I251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2G-01A-11D-A38Z-09 chr16:24192128 C>T maps to NM_002738.6 N471N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr3:53218938 C>T maps to NM_212539.1 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr19:54409604 C>A maps to NM_002739.3 S600*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr19:54403678 C>T maps to NM_002739.3 Y460Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr19:54395786 G>A maps to NM_002739.3 E237E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UD-01A-11D-A307-09 chr3:169988341 T>A maps to NM_002740.5 L195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr10:6540469 G>A maps to NM_006257.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JL-01A-11D-A36J-09 chr1:2077515 C>T maps to NM_002744.4 D201D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr14:30046617 G>A maps to NM_002742.2 I855I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr8:48733395 G>A maps to NM_006904.6 Q3073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr8:48845609 T>G maps to NM_006904.6 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JK-01A-11D-A36J-09 chr8:48739409 G>A maps to NM_006904.6 Q2863*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr8:48866456 G>A maps to NM_006904.6 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr10:52751153 G>T maps to NM_001098512.1 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:179315107 C>T maps to NM_003690.4 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr5:35084605 G>A maps to NM_000949.4 F113F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UC-01A-11D-A307-09 chr21:48083354 A>T maps to NM_206962.1 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr12:3678669 C>A maps to NM_019854.3 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EI-01A-11D-A33E-09 chr19:36297634 C>T maps to NM_021232.1 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:71830638 G>A maps to NM_001126128.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr20:5294712 C>T maps to NM_144773.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr19:54625278 C>T maps to NM_015629.3 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr12:50036711 G>A maps to NM_001031698.1 Q685Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr20:62614399 C>T maps to NM_012469.3 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AK-01A-21D-A24N-09 chr17:1559968 G>T maps to NM_006445.3 T1864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:1557275 G>A maps to NM_006445.3 R2008*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr19:50100900 G>A maps to NM_020719.1 A1103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr5:120021755 C>T maps to NM_016644.1 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr19:5783471 G>A maps to NM_001134316.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr16:29824914 G>A maps to NM_145239.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr7:142459861 C>T maps to ENST00000486171 N160N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr7:142459735 G>T maps to ENST00000486171 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr6:84234188 G>A maps to NM_153362.2 S343S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DX-A1L0-01A-11D-A24N-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-JV-A5VF-01A-11D-A29N-09 chr16:31097416 G>A maps to NM_001039503.2 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:79321686 G>A maps to NM_015225.2 Q1835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr19:40900052 G>T maps to NM_181882.2 P1402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MO-A47R-01A-11D-A24N-09 chr19:40902641 C>T maps to NM_181882.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:104171536 C>T maps to NM_002779.3 Q623Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr10:104174765 G>T maps to NM_002779.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr5:139216823 G>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:227071404 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr19:43383688 C>T maps to NM_006905.2 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MO-A47R-01A-11D-A24N-09 chr19:43262152 C>T did not map to a codon.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr8:87076844 A>T maps to ENST00000276616 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr6:32808750 C>G maps to NM_148919.3 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr7:102988197 G>T maps to NM_002803.2 E14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr16:74339213 T>A maps to NM_002811.3 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr2:54152726 C>T maps to NM_014614.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr21:40552219 G>A maps to NM_003720.2 S128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr13:20325549 T>C maps to NM_001042414.1 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr7:99017739 A>G maps to NM_001198879.1 I700I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48K-01A-11D-A307-09 chr7:99022879 G>A maps to NM_001198879.1 A474A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UC-01A-11D-A307-09 chr23:23397789 A>G did not map to a codon.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr23:23410953 T>A did not map to a codon.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr1:11579881 G>A maps to NM_020780.1 E715E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VF-01A-11D-A29N-09 chr6:42893005 G>A maps to NM_138296.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:16553078 C>T maps to NM_030664.3 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr1:117509803 G>A maps to NM_020440.2 E637E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DN-01A-12D-A27P-09 chr2:209302605 G>A maps to NM_005048.2 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr8:27296913 C>T maps to NM_004103.3 F611F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr6:43113068 T>C maps to NM_002821.3 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr9:96860234 G>T maps to ENST00000434261 E463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DL-01A-11D-A26G-09 chr4:87685825 C>A maps to NM_080685.2 I1366I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:214556692 G>A maps to NM_005401.4 S835S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr1:114372222 T>A maps to NM_015967.5 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr3:47452008 G>A maps to NM_015466.2 P907P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr9:112172682 C>T maps to NM_002829.3 E442E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:18759454 C>T maps to NM_032781.3 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:202127346 C>A maps to ENST00000309017 E174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:3016352 C>T maps to NM_002836.3 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:3017817 G>A maps to NM_002836.3 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr12:70988328 C>T maps to NM_001109754.1 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr12:70988262 C>T maps to NM_001109754.1 W500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:198685877 G>A maps to ENST00000271610 T453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:67203473 G>A maps to NM_005608.2 H117H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr1:44054429 C>T maps to NM_002840.3 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:62189326 C>T maps to NM_002841.3 Q620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:48177362 C>T maps to NM_002843.3 S1080S. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-PC-A5DL-01A-11D-A26G-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr18:8380422 C>T maps to NM_001105244.1 Q1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:220164891 G>A maps to NM_002846.3 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:157931049 G>A maps to NM_002847.3 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:157959836 C>T maps to NM_002847.3 K232K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr20:40735527 G>A maps to ENST00000373198 A1118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr20:41306779 A>T maps to ENST00000373198 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr1:29630535 C>T maps to NM_005704.4 Y892Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:29611336 C>T maps to NM_005704.4 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:121668615 C>T maps to NM_002851.2 Q1667*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:121668614 C>T maps to NM_002851.2 F1666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71P-01A-12D-A33E-09 chr21:46276196 G>A maps to NM_004339.2 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:45162065 C>T maps to NM_006505.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr19:45150756 C>T maps to NM_006505.3 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr21:45539346 G>A maps to NM_005049.2 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr8:52321891 G>A maps to NM_144651.4 P764P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr8:52321600 G>C maps to NM_144651.4 L861L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr8:52321338 G>A maps to NM_144651.4 Q949*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr8:52287284 G>A maps to NM_144651.4 Y1188Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr8:52284448 C>T maps to NM_144651.4 W1295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr8:144688240 C>T maps to NM_023078.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ET-01A-11D-A36J-09 chr15:55838427 G>A maps to NM_015617.1 N351N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DK-01A-11D-A27P-09 chr12:9311087 C>T maps to NM_002864.2 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:9305771 G>A maps to NM_002864.2 L1314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr20:3146262 C>T maps to NM_014731.2 K401K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr17:74283965 G>A maps to NM_032134.1 Q1105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr17:74288738 A>T maps to NM_032134.1 L524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr11:32955584 C>A maps to NM_001076786.1 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr3:113804663 C>T maps to ENST00000485050 Y399Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr2:136373730 C>T maps to ENST00000409606 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J1-01A-11D-A21Q-09 chr12:57693913 G>A maps to ENST00000438036 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr12:57674221 C>T maps to ENST00000438036 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr8:61496780 C>T maps to NM_002865.1 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr18:9815150 G>A maps to NM_006868.3 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:87908393 C>T maps to NM_022337.2 W53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:41292579 C>T maps to ENST00000419646 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:16222761 G>A maps to NM_005370.4 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23V-01A-11D-A29N-09 chr23:103080613 G>T did not map to a codon.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr23:103080662 C>A did not map to a codon.
Sequencing variant TCGA-DX-A6BH-01A-12D-A307-09 chr17:5253800 G>A maps to NM_004703.4 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:114398550 C>T maps to ENST00000409875 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr7:4917281 C>T maps to NM_018059.4 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:4862079 G>A maps to NM_018059.4 I520I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr11:36615529 A>T maps to NM_000536.3 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:17701766 C>T maps to ENST00000395776 V1835V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ER-01A-11D-A36J-09 chr14:36277945 G>T maps to NM_194301.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr20:20620467 G>T maps to NM_020343.3 C209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr8:85800007 G>A maps to NM_001100391.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr2:109384557 T>A maps to NM_006267.4 V2521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr19:5918596 G>C maps to NM_007322.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:21938037 C>T maps to NM_001145658.1 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr23:131351129 A>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:48131350 C>T maps to NM_001098531.2 *924*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:22259604 C>T maps to ENST00000344041 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr11:47460329 C>T maps to NM_005055.3 K373K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr3:25622050 C>T maps to NM_000965.3 D208D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:167929063 C>T maps to NM_002887.3 F337F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr6:88228562 C>A maps to NM_020320.3 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:85597672 C>T maps to NM_152573.2 K714K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:179564926 G>A maps to NM_175062.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr15:79310204 G>A maps to NM_002891.4 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr15:79350741 G>A maps to NM_002891.4 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:49225153 G>A maps to NM_017805.2 A883A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr13:27847333 C>T maps to NM_206827.1 I144I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr12:26218074 A>T maps to NM_001164747.1 K250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:86198701 C>T maps to NM_005447.3 K362K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr12:86198967 T>A maps to NM_005447.3 K274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr13:48947562 C>T maps to NM_000321.2 Q384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr13:48955393 C>T maps to NM_000321.2 Q504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I0-01A-11D-A38Z-09 chr13:48919299 T>A maps to NM_000321.2 Y155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I3-01A-11D-A38Z-09 chr13:49050979 G>A did not map to a codon.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr13:49037971 G>A did not map to a codon.
Sequencing variant TCGA-DX-A7EN-01A-11D-A38Z-09 chr13:49033885 G>T maps to NM_000321.2 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr13:48953786 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr13:48939107 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr13:48947628 G>A did not map to a codon.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr13:48953729 C>T maps to NM_000321.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr13:48947578 T>G maps to NM_000321.2 L389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr13:48954209 C>T maps to NM_000321.2 Q471*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr13:49039373 C>T maps to NM_000321.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr13:48955537 C>T maps to NM_000321.2 R552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48U-01A-11D-A307-09 chr7:5104322 A>G maps to NM_021163.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:5104175 C>T maps to NM_021163.3 H363H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr23:16875808 C>A did not map to a codon.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr23:16875793 C>G did not map to a codon.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr23:47039356 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr23:47035946 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:66384353 C>T maps to NM_001198845.1 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr6:155152086 G>A maps to NM_014892.3 P724P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr12:114384226 A>G maps to NM_016196.3 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr23:48434969 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:155473577 C>T maps to NM_053043.2 I181I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr7:155457899 C>T maps to NM_053043.2 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:50152991 G>A maps to NM_005778.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K6-01A-11D-A21Q-09 chr11:7110542 C>T maps to NM_014469.4 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr11:7110701 C>A maps to NM_014469.4 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X2-A95T-01A-11D-A37C-09 chr10:48389029 G>A maps to NM_002900.2 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:66612481 C>T maps to NM_005133.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr14:103059660 C>T maps to NM_015156.2 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:55568078 C>T maps to NM_001145971.1 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr5:112222763 G>T maps to NM_005669.4 V156V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LU-01A-11D-A21Q-09 chr11:65429467 G>A maps to NM_021975.3 S42S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr7:103276803 G>T maps to ENST00000428762 Y727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr7:103183202 G>A maps to ENST00000428762 R2216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr7:103183260 G>A maps to ENST00000428762 I2196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:103301974 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr7:103301847 C>T maps to ENST00000428762 G472G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DX-A1L1-01A-11D-A24N-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:8601373 C>T maps to NM_012102.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr10:43615161 C>A maps to NM_020975.4 S859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:108476005 G>A maps to NM_032579.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr6:111688529 G>T maps to NM_002912.3 S2154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2IZ-01A-11D-A21Q-09 chr6:111680106 A>C maps to NM_002912.3 S2330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr6:111688939 T>C maps to NM_002912.3 E2017E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr19:1819987 C>T maps to NM_020695.3 V865V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr9:136272154 C>T maps to NM_020385.2 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr9:136272960 C>A maps to NM_020385.2 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr16:74662524 G>A maps to NM_018124.3 A598A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:117198533 C>T maps to NM_173560.3 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EH-01A-11D-A24N-09 chr23:109695943 A>T did not map to a codon.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr23:71349948 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr6:33263136 G>A maps to NM_004761.3 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42W-01A-11D-A24N-09 chr19:11526772 G>A maps to NM_001161616.1 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:24034330 G>A maps to ENST00000382833 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr2:108479403 G>T did not map to a codon.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr2:108487750 A>G maps to NM_182588.2 R1097R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:121275050 G>A maps to NM_001005339.1 H123H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr1:192127850 A>T maps to NM_130782.2 S28S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3NJ-01A-11D-A21Q-09 chr1:192778204 C>T maps to NM_002923.3 Q2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:101065131 G>A maps to NM_015668.3 L529L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr9:116359103 G>A maps to NM_144488.4 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr9:116356456 C>A maps to NM_144489.2 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr14:72924985 A>C maps to NM_004296.4 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:74474926 C>T maps to NM_024599.5 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr3:129249824 C>T maps to NM_000539.3 G156G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:49413013 G>A maps to NM_001664.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr23:119293220 G>A did not map to a codon.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr12:130919311 G>A maps to NM_015347.4 D723D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BK-01A-11D-A37C-09 chr12:130921758 G>A maps to NM_015347.4 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:130926492 C>T maps to NM_015347.4 K451K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr22:20458607 C>A maps to NM_015672.1 P898P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EK-01A-11D-A24N-09 chr6:72960726 C>T maps to NM_014989.4 R826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr11:66101438 C>A maps to NM_004292.2 R514R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr14:93107612 C>T maps to NM_024832.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr14:93119341 C>T maps to NM_024832.3 Q650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr18:21055004 C>T maps to NM_003831.3 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:155874290 T>A maps to ENST00000368322 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr1:40661332 G>A maps to NM_012421.3 G168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:73812543 G>A did not map to a codon.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr23:73812715 C>A did not map to a codon.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr23:73812193 A>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:5300361 C>T maps to NM_134441.1 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr16:67685130 G>A maps to NM_001013838.1 E742E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr14:21058864 T>A maps to NM_001024822.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr1:182544664 A>G maps to NM_021133.3 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2P-01A-11D-A387-09 chr5:31526228 G>A maps to NM_013235.4 R271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:59323146 C>T maps to ENST00000434298 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J0-01A-11D-A21Q-09 chr23:119005265 C>T did not map to a codon.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr18:29648271 A>T maps to NM_017831.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr23:105970350 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:74521251 G>A maps to NM_001098638.1 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr17:78338307 C>G maps to NM_020914.4 P3991P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr17:78360609 C>T maps to NM_020914.4 T4996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr17:78272138 G>A maps to NM_020914.4 V726V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr9:36390529 G>A maps to NM_022781.4 F32F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:56600344 G>A maps to NM_194359.1 I280I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr12:117217131 C>T maps to NM_001109903.1 I287I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:494992 G>A maps to NM_203389.1 A396A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-QC-A7B5-01A-11D-A33E-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr3:77638019 G>A maps to ENST00000332191 L873L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr11:124766915 G>A maps to NM_019055.5 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr11:62381817 C>T maps to NM_000327.3 Q227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr9:94499671 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:151780028 G>A maps to ENST00000392697 I546I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr8:55541921 C>G maps to NM_006269.1 S1827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr8:55534122 C>T maps to NM_006269.1 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:10465862 G>A maps to NM_178857.5 A1915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:10468037 C>T maps to NM_178857.5 T1190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:10465861 G>A maps to NM_178857.5 Q1916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XQ-01A-11D-A37C-09 chr17:1782516 T>A maps to NM_002945.3 Y256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr23:96140082 G>C did not map to a codon.
Sequencing variant TCGA-3B-A9HZ-01A-11D-A38Z-09 chr16:53691421 C>T maps to NM_015272.2 E508E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr12:113327845 C>A maps to NM_001143854.1 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:8706303 C>T maps to NM_000990.4 Y61Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:55898032 T>G maps to NM_001136135.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr23:100646801 C>T did not map to a codon.
Sequencing variant TCGA-MJ-A68J-01A-11D-A307-09 chr23:100646747 C>T did not map to a codon.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr16:2003014 C>T maps to NM_005061.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:150444276 C>T maps to NM_015203.3 T951T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:58904509 C>T maps to NM_001009.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:26878195 C>T maps to NM_001006665.1 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr14:75375802 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr1:152128044 G>A maps to NM_001122965.1 H510H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr1:152127867 A>G maps to NM_001122965.1 Y569Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:99131847 G>A maps to NM_015179.3 T775T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr11:6621897 C>T did not map to a codon.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr23:18660177 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:48562158 C>T maps to NM_018346.1 T422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:48560723 C>T maps to NM_018346.1 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:48560722 C>T maps to NM_018346.1 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr11:77378473 G>A maps to NM_016578.3 R1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr15:55483212 A>G maps to NM_016304.2 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr21:43905898 G>A maps to NM_080860.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:38082234 G>A maps to NM_001038633.2 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A67I-01A-31D-A307-09 chr14:101348434 G>A maps to NM_001134888.2 T897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr14:101350315 G>A maps to NM_001134888.2 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr14:60193760 C>A maps to NM_021136.2 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr3:46539581 A>G maps to NM_031440.1 Q10Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr18:67671406 G>A maps to NM_173630.3 Q2221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42W-01A-11D-A24N-09 chr18:67836096 C>A maps to NM_173630.3 G561G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V2-01A-11D-A32I-09 chr6:45390498 G>T maps to ENST00000359524 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr1:25229149 C>T maps to NM_001031680.2 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr1:25291021 G>T maps to NM_001031680.2 S14*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr9:35560482 C>T maps to NM_001135999.1 I1282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr19:49514350 G>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr6:33162789 G>A maps to ENST00000374685 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr19:38951108 C>T maps to NM_000540.2 R819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr19:39077991 G>T maps to NM_000540.2 E5017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr19:39075731 C>T maps to NM_000540.2 I4932I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DN-01A-12D-A27P-09 chr19:38954157 C>T maps to NM_000540.2 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr19:38959745 C>T maps to NM_000540.2 S1174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:38937390 G>A maps to NM_000540.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:39034457 G>A maps to NM_000540.2 W3985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LU-01A-11D-A21Q-09 chr1:237551405 T>C maps to NM_001035.2 D232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr1:237863630 G>A maps to NM_001035.2 Q3077Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr1:237527673 T>A did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:237758893 G>A maps to NM_001035.2 V1511V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr1:237806667 C>T maps to NM_001035.2 S2421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:237758909 C>T maps to NM_001035.2 L1517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:237829882 C>T maps to NM_001035.2 D2836D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:237811831 G>A maps to NM_001035.2 G2477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:237754097 C>T maps to NM_001035.2 L1322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:33928629 G>A maps to NM_001036.3 G1145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:34030742 C>T maps to NM_001036.3 H2536H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71P-01A-12D-A33E-09 chr15:33954924 C>T maps to NM_001036.3 L1732L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr15:34042400 C>A maps to NM_001036.3 T2771T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr15:34028477 C>G maps to NM_001036.3 L2489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:153580150 C>T maps to NM_080388.1 K57K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I3-01A-11D-A38Z-09 chr1:153430302 G>A maps to NM_002963.3 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:33292386 T>C maps to NM_022753.2 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr1:101704602 C>T maps to NM_001400.4 N21N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr11:18257398 G>A maps to NM_006512.3 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr13:23912515 G>A maps to NM_014363.4 S1833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr19:5616450 G>A maps to NM_014649.2 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr2:234255545 C>T maps to NM_000541.4 D402D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:134990643 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:51171430 G>A maps to ENST00000251020 T1189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr16:51175550 G>A maps to ENST00000251020 N194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:21993213 C>T maps to NM_005407.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr18:76753934 G>A maps to NM_171999.2 P648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr10:76936170 G>A maps to ENST00000372690 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JK-01A-11D-A36J-09 chr7:92735359 C>T maps to NM_017654.3 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UA-01A-12D-A307-09 chr10:71921381 T>C maps to NM_020150.4 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UC-01A-11D-A307-09 chr9:136594925 G>A maps to NM_007101.3 H292H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr17:26708339 G>T maps to ENST00000379061 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr1:109777944 G>A maps to ENST00000369923 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:108939019 G>A maps to NM_014706.3 S208S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr6:148869495 G>T maps to NM_015278.3 V1182V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr3:18390963 G>A maps to ENST00000332610 Q698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr23:84363260 C>T did not map to a codon.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr23:84349149 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9I0-01A-11D-A38Z-09 chr19:1111505 C>G maps to NM_014963.2 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr15:75305126 C>T maps to ENST00000361900 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr6:28540108 A>T maps to NM_052923.1 L1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr3:47470001 C>T did not map to a codon.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr12:125267312 C>T maps to NM_005505.4 K482K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:1538894 G>A maps to NM_003693.2 A550A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr22:20780111 G>A maps to NM_153334.4 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:83601975 G>A maps to NM_001037582.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr13:78130761 G>A maps to NM_144777.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:78171700 C>T maps to NM_144777.2 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B7-01A-11D-A307-09 chr14:31091600 G>A maps to ENST00000311943 Q27Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U7-01A-11D-A29N-09 chr11:62066449 C>G maps to NM_206998.1 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3NK-01A-11D-A21Q-09 chr6:25701445 C>T maps to NM_006998.3 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:38835492 G>A maps to NM_006514.2 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:38835267 G>A maps to NM_006514.2 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:38768306 C>T maps to NM_006514.2 E959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:38783838 G>A maps to NM_006514.2 A683A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr3:38938440 G>A maps to ENST00000302328 C766C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr3:38991679 G>T maps to ENST00000302328 A58A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:38938428 G>A maps to ENST00000302328 I770I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:166850926 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:166848834 G>A maps to NM_001165963.1 I1650I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr2:166168533 G>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:38645321 T>A maps to NM_001099404.1 K591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr2:167263046 C>T maps to NM_002976.2 K1364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:167301397 C>T maps to NM_002976.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr12:52159700 C>T maps to NM_014191.2 R931*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr12:52145166 G>A maps to NM_014191.2 P720P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr2:167138318 C>A did not map to a codon.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr12:6464554 C>T maps to NM_001159576.1 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:23197732 C>T maps to NM_001039.3 S47S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:53516324 C>T maps to NM_002979.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr2:175287647 C>T maps to NM_024583.4 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:43715969 G>A maps to NM_173050.2 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr8:97620691 C>T maps to NM_002998.3 L146L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr11:61205585 G>T did not map to a codon.
Sequencing variant TCGA-DX-A23T-01A-11D-A26G-09 chr7:4091395 C>T maps to NM_152744.3 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr7:4169646 C>G maps to NM_152744.3 Y1349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr17:71431718 G>C maps to NM_001144952.1 T355T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr17:71415396 G>A maps to NM_001144952.1 I698I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:192700930 G>A maps to NM_004657.5 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr12:57317652 T>C maps to NM_148897.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K6-01A-11D-A21Q-09 chr12:57327964 G>A maps to NM_148897.2 Y27Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr12:113875882 G>T maps to NM_138432.2 *330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:75186901 C>T maps to NM_001039573.2 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:30863007 C>T maps to NM_174975.4 L160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr22:30887888 C>T maps to NM_174977.3 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JK-01A-11D-A36J-09 chr16:5061241 C>A maps to NM_014692.1 Y649*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr16:5047001 G>C maps to NM_014692.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:177936954 C>T maps to NM_033127.2 G54G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr1:145112519 G>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:108222574 C>T maps to NM_007214.4 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr9:91964805 C>T maps to NM_024077.3 H618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V2-01A-11D-A32I-09 chr15:49301540 G>T maps to NM_001193489.1 L633L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr4:25806366 C>T maps to NM_015187.3 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:169697009 G>A maps to NM_000450.2 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr1:169572297 C>T maps to NM_003005.3 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2G-01A-11D-A38Z-09 chr1:169586353 G>A maps to NM_003005.3 C131C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr7:83739785 C>T maps to NM_006080.2 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:52473940 G>A maps to NM_020163.1 I439I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:90767144 C>T maps to NM_198925.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EQ-01A-11D-A387-09 chr9:92006298 T>C maps to NM_006378.3 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr5:9202170 C>A maps to NM_003966.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr5:9063188 C>A maps to NM_003966.2 G776G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr5:115822488 G>A maps to ENST00000257414 N306N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DO-01A-11D-A26G-09 chr5:115838003 C>T maps to ENST00000257414 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr15:48055235 G>T maps to NM_153618.1 E228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LT-01A-12D-A21Q-09 chr3:185316762 A>T maps to ENST00000427465 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:30456070 G>A maps to ENST00000478753 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr1:67891959 G>A maps to NM_001018067.1 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:79439605 G>A maps to NM_001174072.1 F422F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:94756285 C>T maps to NM_001100607.1 G215G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:95085652 G>A maps to ENST00000393080 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr14:95030337 C>T maps to NM_006215.2 Y173Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr14:94772437 G>A maps to NM_001756.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:105279333 C>T did not map to a codon.
Sequencing variant TCGA-DX-A2IZ-01A-11D-A21Q-09 chr6:2840712 T>G maps to NM_030666.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr18:61328303 A>C maps to NM_006919.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5Y8-01A-11D-A29N-09 chr6:2890726 A>G maps to NM_004155.4 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr22:21133932 G>A maps to NM_000185.3 G111G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr17:1657572 C>T maps to NM_000934.3 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:57381829 C>T maps to ENST00000403558 L470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr2:64863597 G>C maps to NM_014755.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:30977487 C>T maps to NM_014712.1 S762S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:30976496 G>A maps to NM_014712.1 E478E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:30978302 G>A maps to NM_014712.1 K868K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr14:99865105 G>T maps to NM_032233.2 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EH-01A-11D-A24N-09 chr3:9476151 C>T maps to ENST00000407969 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:150923308 C>T maps to NM_001145415.1 F652F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr22:26688804 C>T maps to NM_021115.4 S176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:26743808 C>T maps to NM_021115.4 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr22:26736437 C>T maps to NM_021115.4 Y684Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr22:26707839 C>T maps to NM_021115.4 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V2-01A-11D-A32I-09 chr16:29891248 G>T maps to NM_201575.2 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:65826321 C>T maps to NM_006842.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:65826320 C>T maps to NM_006842.2 N329N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MO-A47R-01A-11D-A24N-09 chr16:70595540 C>G maps to NM_012426.4 A714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2L-01A-32D-A417-09 chr3:52941738 G>T maps to NM_016329.3 Y639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr21:33057902 G>A maps to NM_020706.2 F729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:46357926 G>A maps to NM_004719.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr13:23853609 A>T maps to NM_000231.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr3:153909092 C>A maps to NM_015595.3 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A3OV-01A-11D-A228-09 chr3:153935689 G>A maps to NM_015595.3 K626K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr8:8234394 G>A maps to NM_001080826.1 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr2:201437696 T>A maps to NM_152524.5 C876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UD-01A-11D-A307-09 chr22:25251312 C>T maps to NM_001039948.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:25251312 C>T maps to NM_001039948.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr17:2268615 C>T maps to NM_014853.2 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr1:156777008 G>A maps to NM_001161441.1 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5YA-01A-11D-A29N-09 chr1:21053558 G>A maps to ENST00000444387 R74*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:78393344 C>T maps to NM_001101404.1 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:78390432 C>T maps to NM_001101404.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr23:80532630 T>C did not map to a codon.
Sequencing variant TCGA-WK-A8XS-01A-11D-A37C-09 chr5:171766854 C>T maps to NM_001017995.2 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:145439744 C>T maps to NM_152550.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:8221203 C>T maps to NM_018986.3 G353G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr19:51219978 G>A maps to ENST00000391814 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:70666653 G>A maps to ENST00000338508 C437C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr11:70332047 C>A maps to ENST00000338508 S1444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr8:145154475 C>T maps to NM_030974.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr17:7534624 C>T maps to NM_001040.3 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U8-01A-11D-A29N-09 chr13:26621169 G>A maps to NM_001007538.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr4:42403179 A>C maps to NM_001080505.1 T143T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr4:42403080 C>T maps to NM_001080505.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr23:601771 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr3:157820520 G>A maps to NM_003030.4 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X2-A95T-01A-11D-A37C-09 chr3:157816013 C>T maps to NM_003030.4 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr23:9905383 G>C did not map to a codon.
Sequencing variant TCGA-DX-AB36-01A-11D-A417-09 chr23:9862479 G>A did not map to a codon.
Sequencing variant TCGA-JV-A5VF-01A-11D-A29N-09 chr23:9905319 A>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:9863007 C>T did not map to a codon.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr23:9905684 C>G did not map to a codon.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr23:50350910 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:164739171 C>T did not map to a codon.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr3:113325931 C>T maps to ENST00000393830 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr11:117064672 C>T maps to NM_001040455.1 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:405991 C>T maps to NM_021805.2 E379E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:52002722 G>A maps to NM_053003.2 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr19:52031484 A>G maps to NM_001245.5 G345G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2J-01A-11D-A387-09 chr19:52031507 C>T did not map to a codon.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr19:51649284 C>T maps to NM_014385.2 L312L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:51647684 C>T maps to NM_014385.2 I152I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:51960874 C>T maps to NM_014442.2 W191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr19:51629010 C>A maps to NM_014441.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr21:44839072 C>T maps to NM_173354.3 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K6-01A-11D-A21Q-09 chr21:44836771 A>T maps to NM_173354.3 I734I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr21:44839292 G>A maps to NM_173354.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr12:56355453 G>A maps to NM_006928.3 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr12:56355131 C>T maps to NM_006928.3 Q101Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:100898229 G>A maps to ENST00000262901 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr6:100868710 C>A maps to ENST00000262901 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LW-01A-21D-A21Q-09 chr15:75722671 G>A maps to NM_001145357.1 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:72152077 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:232568108 G>A maps to NM_020808.3 P1380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:38682898 G>A maps to NM_015073.1 K1515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:38682937 G>A maps to NM_015073.1 E1528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:1460519 G>A maps to NM_001122962.1 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr20:1460498 G>A maps to NM_001122962.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:69648753 G>A maps to NM_012238.4 W221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:39371790 G>A maps to NM_012237.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr11:218992 G>A maps to NM_012239.5 R340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:35650021 C>T maps to NM_014450.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr6:31931479 G>A maps to NM_006929.4 K539K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr5:54624534 G>A maps to NM_015360.4 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:54654444 G>A maps to NM_015360.4 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr13:78318544 C>T maps to ENST00000389459 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr4:48380034 C>T maps to NM_020846.1 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:160589631 C>T maps to NM_003037.2 T266T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DO-01A-11D-A26G-09 chr23:153717081 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr4:87744873 G>A maps to NM_197965.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr16:56901058 C>T maps to NM_000339.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C3-01A-11D-A36J-09 chr16:56914082 C>T maps to NM_000339.2 F495F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr16:67985100 G>A maps to NM_005072.4 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr20:44669253 G>A maps to ENST00000372315 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr20:44685179 C>T maps to NM_001134771.1 I1052I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr5:1075559 G>A maps to NM_006598.2 F631F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr5:1081839 G>A maps to NM_006598.2 Y383Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:26817365 G>A maps to NM_001145975.1 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VD-01A-42D-A38Z-09 chr7:135377096 G>C maps to NM_012450.2 V398V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:121634084 G>A maps to NM_021082.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:121647305 C>T maps to NM_021082.3 F415F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:73744246 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr23:73641839 T>A did not map to a codon.
Sequencing variant TCGA-UE-A6QT-01A-12D-A32I-09 chr17:66267496 G>A maps to NM_004694.4 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr6:25862062 G>A maps to NM_001098486.1 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3B-01A-11D-A417-09 chr6:25777119 C>T maps to NM_005495.2 L401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V2-01A-11D-A32I-09 chr8:20004810 G>T maps to NM_001135691.2 L474L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr21:46951893 G>A maps to NM_194255.1 Q120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:228563863 G>A maps to NM_025243.3 F189F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr2:113414762 C>T maps to NM_005415.3 F241F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr6:160575835 C>T maps to NM_003057.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:63057945 G>A maps to NM_001039752.3 G103G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48L-01A-11D-A307-09 chr14:23818511 A>G maps to NM_020372.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:62863493 G>A maps to NM_001136506.1 R347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:62849037 G>A maps to NM_001136506.1 T462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:62931544 C>T maps to NM_199352.3 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:131719896 C>T maps to ENST00000435065 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr9:19516345 A>G maps to NM_020344.2 A597A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:172712395 G>A maps to NM_003705.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr12:98989562 C>A maps to NM_213611.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr12:98987854 C>T maps to NM_213611.2 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr8:104417073 C>T maps to NM_030780.3 K107K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:6433608 G>A maps to NM_173637.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:1505533 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:1508617 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr7:107353039 G>A maps to NM_000441.1 T764T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr7:107330648 G>A maps to NM_000441.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr6:35945037 G>A maps to NM_052961.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EQ-01A-11D-A387-09 chr1:205897158 C>T maps to NM_134325.2 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr1:205898418 G>T maps to NM_134325.2 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr1:205897104 G>A maps to NM_134325.2 I342I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr15:50515325 T>C maps to NM_003645.3 G379G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr9:131107638 C>T maps to NM_005094.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68J-01A-11D-A307-09 chr5:128302183 C>T maps to NM_001017372.1 F118F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:45559940 G>A maps to NM_004212.3 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr9:86909132 G>A maps to NM_022127.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr7:5336736 C>A maps to NM_153247.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr9:136340689 C>T maps to NM_017585.3 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr9:136343453 T>C maps to NM_017585.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:27480069 G>A maps to NM_003459.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr4:42003738 G>A maps to NM_006345.3 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J1-01A-11D-A21Q-09 chr9:115923900 C>T maps to ENST00000394724 I118I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr20:37356948 C>T maps to NM_080552.2 R415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr5:176815282 C>T maps to NM_003052.4 D282D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2H-01A-11D-A38Z-09 chr3:112300121 G>A maps to NM_017945.2 R386R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr5:150696515 G>A maps to NM_181776.2 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U5-01A-11D-A228-09 chr23:48321357 A>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:48318259 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:84070430 G>A maps to NM_001080442.1 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr9:108123580 C>T maps to NM_080546.3 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr9:108120649 A>T maps to NM_080546.3 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr1:75669435 T>C maps to NM_001130058.1 E710E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr17:19618455 C>T maps to NM_152908.3 E66E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr17:19611113 G>A maps to NM_152908.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr17:42327872 C>A maps to NM_000342.3 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr2:162719572 G>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:162821568 C>T maps to NM_001178015.1 A1015A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr2:162735639 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:162751302 C>T maps to NM_001178015.1 R437*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LT-01A-12D-A21Q-09 chr4:72412085 T>A maps to NM_001098484.2 L821*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2H-01A-11D-A38Z-09 chr4:72332162 C>T maps to NM_001098484.2 G500G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr4:72412065 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:74480150 G>A maps to NM_021196.3 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr5:139743760 C>T maps to ENST00000507527 F483F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr16:24895406 C>T maps to NM_052944.2 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr16:24918470 G>T maps to NM_052944.2 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr21:35469188 A>G maps to NM_006933.4 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:27428923 C>T maps to NM_021095.2 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr5:1238114 C>G maps to NM_182632.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr5:1238153 C>T maps to NM_182632.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr5:1244845 G>A maps to NM_182632.2 W540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QT-01A-12D-A32I-09 chr3:45801482 G>T maps to NM_020208.3 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42X-01A-11D-A24N-09 chr5:1432616 G>A maps to NM_001044.4 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr3:14487300 C>G maps to NM_001134367.1 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48U-01A-11D-A307-09 chr3:170216673 C>T did not map to a codon.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr23:70147135 G>A did not map to a codon.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr22:21385528 G>C maps to NM_004173.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:33353369 G>A maps to NM_014270.4 Q201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:33333196 G>A maps to NM_014270.4 I367I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:40405533 C>T maps to NM_021097.2 E636E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:70515508 G>A maps to NM_183002.1 F794F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr3:111887770 G>A maps to NM_183061.1 R1064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:173490499 G>A maps to NM_178527.3 T893T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QU-01A-11D-A27P-09 chr2:103148831 C>T maps to NM_001011552.3 S694S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:142985704 C>A maps to NM_173653.3 E593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:21428333 G>A maps to NM_134431.3 S545S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:21450398 G>A maps to NM_134431.3 F338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:21370150 G>A maps to NM_006446.4 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr12:21370180 C>G maps to NM_006446.4 V542V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr12:21028280 G>A maps to NM_019844.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:20905386 C>T maps to NM_017435.4 F688F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr11:74911336 G>A maps to NM_007256.4 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr5:101834501 G>C maps to NM_173488.3 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A8OO-01A-11D-A36J-09 chr17:33806525 G>A maps to ENST00000361112 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:33767961 G>A maps to NM_144682.5 N782N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr17:33772390 C>T maps to NM_144682.5 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr17:33592429 T>G maps to NM_144975.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr17:33592321 C>T maps to NM_144975.3 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr4:20525451 T>C maps to ENST00000273739 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:20544138 C>T maps to ENST00000273739 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr5:168123306 A>T maps to NM_003062.2 P1024P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr5:168671749 G>A maps to NM_003062.2 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:168244461 G>A maps to NM_003062.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-AA9N-01A-11D-A38Z-09 chr5:168244434 G>A maps to NM_003062.2 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr13:86368333 T>C maps to NM_032229.2 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr18:12427222 C>T maps to NM_006553.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:59182581 G>A maps to NM_024755.2 R659R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr8:143823299 G>T maps to NM_020427.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr9:2161706 G>T maps to NM_003070.3 E1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VE-01A-11D-A29N-09 chr9:2097413 C>T maps to NM_003070.3 N1007N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:95194790 C>T maps to NM_001128429.1 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr2:217279859 C>T maps to NM_014140.3 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A240-01A-32D-A27P-09 chr12:56565570 G>A maps to NM_003075.3 Q662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr9:106888986 G>A maps to NM_001042550.1 Q839Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:160135716 C>T maps to NM_005496.3 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A3PN-01A-11D-A228-09 chr18:2656091 C>T maps to NM_015295.2 G6G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr16:18840639 G>A maps to ENST00000389467 Q3191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J0-01A-11D-A21Q-09 chr17:2203217 C>A maps to NM_017575.4 G277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:2090027 G>A maps to NM_017575.4 V1028V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:2075957 C>T maps to NM_017575.4 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:183519982 C>T maps to ENST00000367537 S1074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr6:109764230 C>T maps to NM_003080.2 Q226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:68405670 G>A maps to NM_018667.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr1:28282223 G>C maps to NM_014474.2 G240G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:31493283 A>T maps to ENST00000454496 K792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr7:98633222 C>A maps to NM_020429.2 T668T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr2:88387479 C>T maps to NM_198274.3 H138H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr17:1686393 G>C maps to NM_052928.2 R732R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:1704153 G>A maps to NM_052928.2 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr20:48600634 T>C maps to NM_005985.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr20:48600505 C>T maps to NM_005985.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr20:10273569 C>T maps to NM_003081.2 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:10280020 C>T maps to NM_130811.1 I171I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:21224623 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr6:84368741 T>C maps to NM_014841.2 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr6:84290166 A>T did not map to a codon.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr5:176048271 T>C maps to NM_003085.3 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:242002275 C>T maps to NM_001080437.1 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:1079274 G>A maps to NM_018968.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:1371200 C>T maps to NM_018968.3 F525F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr7:17861149 G>A maps to ENST00000417048 H657H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr2:27599043 C>T maps to NM_014748.2 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr4:186180113 G>A maps to NM_031953.2 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:186231898 C>T maps to NM_031953.2 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ER-01A-11D-A36J-09 chr15:75942420 C>G maps to NM_153271.1 Y326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:99157161 G>A maps to NM_015976.4 R182R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr1:179322766 C>A maps to NM_003101.4 Y548*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:76355017 G>A maps to NM_003955.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr9:138586906 C>T maps to NM_001101677.1 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:138588518 C>T maps to NM_001101677.1 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr13:36748879 G>A maps to ENST00000511166 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr13:36765960 C>T maps to ENST00000511166 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:97099063 G>A maps to NM_001034954.1 L897L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr10:108924056 G>T maps to NM_001013031.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr10:107023092 C>T maps to NM_014978.1 S1210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr10:106970990 C>T maps to NM_014978.1 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr10:106974337 G>A maps to NM_014978.1 G838G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:107016626 C>T maps to NM_014978.1 L1130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:121367754 G>A maps to NM_003105.5 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr11:121429443 G>A maps to NM_003105.5 T936T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr14:50623781 G>T maps to NM_006939.2 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr14:50585355 C>T maps to NM_006939.2 Q1235Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr20:307371 C>T maps to NM_006943.2 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr8:55372038 G>A maps to NM_022454.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr23:139586762 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr12:23998926 G>A maps to NM_006940.4 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr8:10584159 C>T maps to ENST00000354846 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr8:10583913 G>A maps to ENST00000354846 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr16:1033835 G>A maps to NM_014587.3 K177K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr2:231152613 G>A maps to NM_007237.4 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:22680839 C>T maps to ENST00000376603 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:22680840 C>T maps to ENST00000376603 Q473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:49075914 C>T maps to ENST00000376407 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr23:140335819 T>A did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr23:140336557 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:140785771 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:140786495 C>T did not map to a codon.
Sequencing variant TCGA-VT-A80J-01A-11D-A36J-09 chr23:140786505 G>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:142795315 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:24797072 C>T maps to ENST00000424834 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DO-01A-11D-A26G-09 chr17:48628216 C>G maps to NM_022827.2 S441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr17:3366053 G>T maps to NM_001170695.1 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr6:44336209 A>C maps to NM_145026.3 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr5:35753863 G>A did not map to a codon.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr2:220353596 G>A maps to NM_005876.4 T2708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:220333749 G>A maps to NM_005876.4 R1157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:16261245 C>T maps to NM_015001.2 I2837I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr15:44876712 G>T maps to NM_025137.3 S1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr15:44925816 G>A maps to NM_025137.3 Q541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr19:49129288 C>T maps to NM_020126.3 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:49129293 C>T maps to NM_020126.3 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr2:228973607 C>T maps to NM_001142644.1 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr23:62570181 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:147692066 C>T maps to NM_032566.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr3:48369804 G>T maps to NM_001080525.1 I9I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr17:4389837 C>T maps to NM_182538.4 Y470Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:32280232 C>T maps to NM_144569.4 G234G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:167675836 G>A maps to NM_016950.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB36-01A-11D-A417-09 chr2:73115590 C>T maps to NM_003124.4 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr15:38641682 C>T maps to NM_152594.2 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr15:38641681 G>T maps to NM_152594.2 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71O-01A-12D-A33E-09 chr19:38886199 C>A maps to NM_001042522.1 G216G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:124322808 G>A maps to NM_199327.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr23:155003565 A>T did not map to a codon.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr23:155003890 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr1:158583575 G>T maps to NM_003126.2 P2308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr1:158585052 C>T maps to NM_003126.2 Q2247Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr14:65253406 G>A maps to ENST00000389723 S1096S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BK-01A-11D-A37C-09 chr14:65234022 A>T maps to ENST00000389723 T2093T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:65240024 C>T maps to ENST00000389723 R1701R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr2:54855379 C>T maps to NM_003128.2 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:54856751 C>T maps to NM_003128.2 I827I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr2:54839467 C>T maps to NM_003128.2 F157F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:41063224 C>T maps to NM_020971.2 T1862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr15:42154052 C>T maps to ENST00000320955 A2539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:30740867 C>T maps to NM_006662.2 D2034D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr22:42276778 A>G maps to NM_004599.2 A607A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J4-01A-32D-A21Q-09 chr12:64377911 C>T maps to NM_020762.2 Q85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:62173582 C>T maps to NM_080823.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr14:35480756 A>G maps to NM_003136.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr7:104844171 T>A maps to ENST00000336613 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:38033464 G>A did not map to a codon.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr23:38031203 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:2806481 G>A maps to NM_016333.3 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr12:119592119 G>T maps to NM_194286.2 R488R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr7:100482416 C>T maps to NM_015908.5 D333D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr18:23612404 T>C maps to ENST00000415083 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr2:182786787 A>G maps to NM_001130445.1 Q1108Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:27958926 C>T maps to NM_033389.2 Q1068Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr11:67075388 G>A maps to NM_017857.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr7:149480379 C>T maps to NM_198455.2 F754F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr7:149506540 T>A maps to NM_198455.2 S3108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr7:149509071 G>A maps to NM_198455.2 R3209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:38679637 G>A maps to NM_001049.2 E348E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr22:37603368 C>T maps to NM_001051.2 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:23017085 C>T maps to NM_001052.2 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr23:48125796 G>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:48117236 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr23:52681340 C>T did not map to a codon.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr23:52682510 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr11:130060352 C>T maps to NM_021978.3 S213S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr8:53073947 T>C maps to NM_014682.2 P527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:53079526 C>T maps to NM_014682.2 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:8747716 G>A maps to NM_005418.3 S460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr3:186760952 G>A maps to NM_003032.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:130670789 G>A maps to NM_175039.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:77510052 G>A maps to NM_030965.1 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr3:52535686 C>A maps to NM_015136.2 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:52538552 C>T maps to NM_015136.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr12:104015857 C>T maps to NM_017564.9 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:36570341 G>A maps to NM_003149.1 G325G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EQ-01A-11D-A387-09 chr3:136261013 G>A maps to NM_005862.2 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr10:17747637 C>T maps to NM_003473.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr10:17738848 C>A maps to NM_003473.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr13:33700361 G>A maps to NM_178007.2 F638F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:67939183 G>A did not map to a codon.
Sequencing variant TCGA-DX-A3LT-01A-12D-A21Q-09 chr12:56743278 C>T maps to NM_005419.3 V424V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UC-01A-11D-A307-09 chr12:56749494 T>C maps to NM_005419.3 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:56740714 C>T maps to NM_005419.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:191919251 C>T maps to NM_003151.2 K405K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:47746545 A>G maps to NM_001048166.1 N528N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AK-01A-21D-A24N-09 chr11:63965442 G>A maps to ENST00000358794 Q387Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C5-01A-11D-A36J-09 chr5:171583762 A>G maps to NM_005990.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:1220482 C>T maps to NM_000455.4 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr2:220473311 C>G maps to NM_052902.2 L548L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:31948443 C>T maps to NM_032454.1 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr8:99539035 G>T maps to ENST00000354930 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr10:134059420 T>A maps to NM_173575.2 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr6:36492186 C>T maps to NM_007271.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:48808300 C>T maps to NM_172311.2 R177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:81837491 G>A maps to NM_033104.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:79977183 C>T maps to ENST00000392359 K72K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr2:37126758 G>A maps to NM_003162.2 F234F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:31658538 C>T maps to NM_178862.1 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr11:59540715 G>A maps to NM_004177.4 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr9:130438120 C>T maps to NM_003165.3 I383I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr9:130438151 C>T maps to NM_003165.3 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:120840490 C>T maps to NM_014980.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr10:104357025 C>T maps to NM_016169.3 Q296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr8:70476321 C>T maps to NM_001128206.1 R38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr8:70533466 G>A maps to NM_001128206.1 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:46300963 G>A maps to NM_001161841.1 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:108881354 C>T maps to NM_001008743.1 I232I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr19:48386832 C>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:44221919 C>T maps to NM_014351.3 K272K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:4452606 C>T maps to NM_182760.3 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:4452605 C>T maps to NM_182760.3 W299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:114804166 G>A maps to NM_022486.3 F741F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:24581169 G>A maps to NM_019601.3 E297E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:33194380 G>A maps to NM_015551.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr23:48559060 C>T did not map to a codon.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr9:113170709 A>T maps to ENST00000374463 G2393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr7:138344682 C>T maps to NM_001139456.1 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:138313073 G>A maps to NM_001139456.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr19:39694753 G>A maps to NM_001080468.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr1:115419371 G>T maps to NM_003176.2 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr1:115487552 C>T maps to NM_003176.2 R702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr6:10935391 G>A maps to NM_001040274.2 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr9:93650107 C>T maps to NM_003177.5 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr9:93606230 C>T maps to NM_003177.5 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr6:152466655 T>C maps to NM_033071.2 V8266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr6:152485348 G>C maps to NM_182961.2 V7913V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB36-01A-11D-A417-09 chr6:152697664 G>A maps to NM_182961.2 Q3059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:152570313 G>A maps to NM_182961.2 P6518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HI-01A-11D-A387-09 chr14:64445578 C>T maps to NM_182914.2 N472N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr14:64465046 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr21:34003352 C>T maps to NM_003895.3 T1597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr6:158485871 G>A maps to NM_003898.3 K458K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr15:99670638 C>T maps to ENST00000336292 L691L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr5:150028886 G>A maps to NM_001166209.1 K594K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr1:110019409 C>T maps to NM_001040709.1 I89I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr12:33538211 C>T maps to NM_198992.3 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:46967596 C>T maps to NM_031912.3 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr10:46965864 G>A maps to NM_031912.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EN-01A-11D-A38Z-09 chr14:62542039 G>A maps to NM_031914.2 E308E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr14:62567268 C>T maps to NM_031914.2 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BK-01A-11D-A37C-09 chr19:51140535 G>T maps to NM_001160329.1 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr18:40853562 G>A maps to NM_020783.3 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-AB3D-01A-12D-A417-09 chr18:40853553 T>C maps to NM_020783.3 R280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr1:114641798 G>C maps to ENST00000369545 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X2-A95T-01A-11D-A37C-09 chr1:114646325 T>C maps to ENST00000369545 G363G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr11:1856622 G>A maps to NM_138567.3 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:7324339 C>T maps to NM_175733.3 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr11:7334913 C>A maps to NM_175733.3 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:99956528 T>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr6:132938843 A>G maps to NM_001033080.1 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr6:132945356 T>A maps to NM_001033080.1 K20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr6:132892362 T>C maps to NM_175067.1 Y301Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:123996962 C>T maps to NM_206862.2 S2727S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr10:123845785 C>T maps to NM_206862.2 S1257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr4:7055967 G>A maps to NM_152293.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A8OO-01A-11D-A36J-09 chr23:70587350 A>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:70595091 C>T did not map to a codon.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr23:70598811 C>T did not map to a codon.
Sequencing variant TCGA-Z4-AAPF-01A-11D-A38Z-09 chr9:32635502 G>A maps to NM_153809.2 S25S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr9:32632964 G>A maps to NM_153809.2 F871F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr9:32632976 G>C maps to NM_153809.2 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:61498205 C>T maps to ENST00000389520 A1631A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:234561433 G>A maps to NM_005646.3 I1143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr15:102215838 G>A maps to NM_152334.2 F584F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr1:6637054 C>T maps to NM_138697.3 R507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr1:19181393 G>A maps to NM_152232.2 H190H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:19166797 G>A maps to NM_152232.2 F605F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:19166407 G>A maps to NM_152232.2 D735D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr7:141673291 G>A maps to NM_176817.4 F66F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:142880795 C>T maps to NM_176881.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:141491050 G>A maps to NM_018980.2 W297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr4:38016302 C>T maps to NM_015173.2 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr4:38119813 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:131554811 C>T maps to NM_018201.3 F114F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB36-01A-11D-A417-09 chr12:72291722 T>A did not map to a codon.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr15:78316557 C>T maps to NM_144572.1 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EI-01A-11D-A24N-09 chr23:106061980 A>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr23:106117041 G>T did not map to a codon.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr1:235577819 G>A maps to NM_003193.3 K86K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr16:2027653 C>T maps to NM_006453.2 R628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:124502103 A>G maps to NM_032811.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:124495737 A>T maps to NM_032811.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr17:59477917 C>T maps to NM_005994.3 I127I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:45819978 G>A maps to NM_013351.1 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:79286458 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr12:115109882 C>T maps to NM_016569.3 A665A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42W-01A-11D-A24N-09 chr12:115112626 G>A maps to NM_016569.3 S371S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr14:92251694 C>A maps to NM_001128596.1 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:102529111 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:102529110 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:2825482 G>A maps to NM_207013.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr1:24078270 G>A maps to NM_003198.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A76Y-01A-11D-A351-09 chr1:24080853 A>G maps to NM_003198.2 S591S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EH-01A-11D-A24N-09 chr18:44559799 C>T maps to NM_016427.2 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr18:44559472 C>T maps to NM_016427.2 A721A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2P-01A-11D-A387-09 chr5:145890059 T>G maps to NM_006706.3 L1051*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr1:152084914 A>G maps to NM_007113.2 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr1:152057568 A>G maps to NM_001008536.1 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HR-01A-11D-A387-09 chr11:67818125 G>A maps to NM_006019.3 L803L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:59629150 T>A maps to NM_001062.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr5:149755996 G>T maps to ENST00000451292 V718V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr5:149758814 C>T maps to ENST00000451292 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr6:44253991 C>T maps to NM_182539.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr4:156835542 G>C maps to NM_005651.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ET-01A-11D-A36J-09 chr9:100240848 A>G maps to NM_014290.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr12:3121376 C>T maps to NM_003213.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:3147171 C>T maps to NM_003213.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr11:120989345 C>T maps to NM_005422.2 A374A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:121030983 C>T maps to NM_005422.2 I1610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr17:6719280 C>T maps to NM_053285.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr17:15215788 C>T maps to NM_031898.2 V296V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:20848596 C>T maps to NM_007110.4 E1600E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr14:20848392 C>G did not map to a codon.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr5:1293551 G>A maps to NM_198253.2 N483N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr1:45811024 A>C maps to NM_007170.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr10:70405281 T>C maps to NM_030625.2 A932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:70450580 C>T maps to NM_030625.2 T1807T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr2:74273484 G>A maps to ENST00000409262 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Q-01A-11D-A38Z-09 chr23:69830389 C>T did not map to a codon.
Sequencing variant TCGA-DX-A23V-01A-11D-A29N-09 chr23:104464404 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:104463703 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr23:107224535 G>T did not map to a codon.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr8:30695393 A>G maps to NM_031271.3 T2419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr3:133467271 C>T maps to NM_001063.3 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr6:50791449 C>A maps to ENST00000263046 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:50810894 C>T maps to ENST00000263046 I400I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr16:4308076 C>A maps to NM_003223.2 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr2:122000042 C>T maps to NM_014553.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr13:114294575 C>T maps to NM_007111.4 D409D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr23:132351354 G>A did not map to a codon.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr23:132352120 T>A did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr7:100224889 G>A maps to NM_003227.3 L664L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr3:195785482 C>A maps to NM_001128148.1 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:133923743 C>T maps to NM_003235.4 I1375I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:95230401 G>A maps to NM_014305.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:41854265 G>A maps to NM_000660.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:30713641 C>T maps to NM_001024847.2 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:105897046 C>A maps to NM_004257.4 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB30-01A-11D-A38Z-09 chr2:105886142 G>A maps to NM_004257.4 G664G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr23:89177281 C>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:89177804 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr14:24731501 G>A maps to NM_000359.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:36760822 G>A maps to NM_004613.2 A565A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr20:2298098 A>G maps to NM_003245.3 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UC-01A-11D-A307-09 chr3:44943113 C>A maps to NM_003241.3 I252I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPF-01A-11D-A38Z-09 chr8:56737231 C>T maps to NM_024831.6 D844D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:71184584 G>A maps to NM_020147.3 H9H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr16:67876993 T>C maps to NM_020457.2 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr5:79351686 G>A maps to NM_003248.4 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LU-01A-11D-A21Q-09 chr5:79355568 C>T maps to NM_003248.4 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr5:79351743 C>G maps to NM_003248.4 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr23:122756708 T>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:175387066 G>A maps to NM_032361.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr17:38240108 C>T maps to NM_003250.5 Q82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:36752121 C>T maps to NM_005119.3 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:36752122 C>T maps to NM_005119.3 Q98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3A-01A-11D-A417-09 chr3:24169080 G>A maps to NM_001128177.1 D351D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr3:24164566 A>G maps to NM_001128177.1 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr3:24164569 A>G maps to NM_001128177.1 D397D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr7:11633080 G>T maps to ENST00000423059 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr7:11676214 G>A maps to ENST00000423059 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr7:11446545 G>T maps to ENST00000423059 C1351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L0-01A-11D-A24N-09 chr2:138378228 C>T maps to ENST00000272643 C1247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:137814296 G>A maps to ENST00000272643 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:138414697 G>A maps to ENST00000272643 W1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr2:137814608 G>T maps to ENST00000272643 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:138414658 G>A maps to ENST00000272643 W1438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UD-01A-11D-A307-09 chr10:121337183 C>T maps to NM_001033925.1 V224V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr21:32598230 G>A maps to NM_003253.2 T540T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr19:4816505 C>T maps to NM_182919.2 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:43785015 G>A maps to NM_005424.2 T1011T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr19:7998994 C>T maps to NM_006351.3 A174A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:47446024 C>T did not map to a codon.
Sequencing variant TCGA-SG-A6Z7-01A-12D-A32I-09 chr3:156396349 C>T maps to NM_015508.4 H288H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr15:30033626 C>T maps to NM_003257.3 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr23:153537745 G>T did not map to a codon.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr23:153537792 A>T did not map to a codon.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr4:164393215 G>T maps to NM_032136.4 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr9:84228346 G>A maps to NM_005077.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr4:166910545 C>T maps to ENST00000507499 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr4:166915614 C>A maps to ENST00000507499 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M2-01A-21D-A228-09 chr15:63097815 C>T maps to NM_015059.2 D2165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr15:62945392 C>T maps to NM_015059.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X2-A95T-01A-11D-A37C-09 chr15:63055878 C>T maps to NM_015059.2 D1693D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr4:38776299 C>T maps to NM_030956.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr4:187003982 G>A maps to NM_003265.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:12939946 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:149089529 G>A maps to ENST00000383054 Q180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr8:105367286 G>A maps to NM_030788.2 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:66531762 G>A maps to ENST00000286424 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr12:50156675 A>G maps to NM_001098576.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:81654618 G>A maps to ENST00000454937 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr17:76113989 C>T maps to NM_007267.6 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:38229551 G>A maps to NM_152453.2 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr12:124069230 C>T maps to NM_006815.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr17:72832222 C>T maps to NM_017728.3 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr7:12271552 T>C maps to NM_018374.3 Y259Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:133099898 C>T maps to NM_001136469.1 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:133099028 C>T maps to NM_001136469.1 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:21102020 A>G maps to NM_003876.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:108985901 C>T maps to NM_181724.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr2:98428882 C>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:126128722 C>T maps to NM_052907.2 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB30-01A-11D-A38Z-09 chr17:32957124 C>T maps to NM_207313.1 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr7:142983669 G>C maps to NM_153345.1 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr2:135470827 T>A maps to NM_030923.4 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:150500763 C>T maps to NM_018487.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr2:103414355 G>A maps to NM_144632.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:202984050 C>T maps to NM_001079809.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr22:38620870 C>T maps to NM_012264.4 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:166006748 C>T maps to NM_001100389.1 E222E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr4:166000893 G>T maps to NM_001100389.1 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:220412612 C>T maps to NM_001005209.1 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr9:74319670 G>A maps to NM_013390.2 R1012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr9:74365129 G>T maps to NM_013390.2 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:140099806 G>A maps to NM_053045.1 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2H-01A-11D-A38Z-09 chr6:37186251 C>A maps to NM_145316.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr23:100349694 G>A did not map to a codon.
Sequencing variant TCGA-3B-A9HL-01A-11D-A387-09 chr3:12778113 G>A maps to ENST00000431022 F196F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:194337952 G>A maps to NM_001166305.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:92032476 G>A maps to NM_018710.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr14:77697933 C>T maps to NM_020431.2 D118D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr17:7758592 C>T maps to NM_203411.1 C67C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr9:136384034 G>A maps to NM_001080483.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:24524038 G>A maps to NM_024893.1 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:154721288 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr23:154736706 G>C did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:69100304 C>T maps to NM_182502.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr4:69343293 T>C maps to NM_014058.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:69344606 C>T maps to NM_014058.3 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr4:68939711 G>A maps to NM_207407.2 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2F-01A-11D-A387-09 chr21:19732161 G>A maps to NM_002772.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr21:19647611 G>A maps to NM_002772.2 L936L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr21:19698791 C>T maps to NM_002772.2 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr21:43815480 G>A maps to ENST00000380399 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr22:37480402 G>A maps to ENST00000381792 A376A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr12:83455573 G>A maps to NM_152588.1 E765E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48N-01A-11D-A307-09 chr13:101264681 T>C maps to NM_032813.2 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5YA-01A-11D-A29N-09 chr11:57505880 C>G maps to NM_015959.3 Y140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr9:117825394 C>T maps to NM_002160.2 T1278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A971-01A-11D-A387-09 chr9:117808687 C>G did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:4652150 C>T maps to NM_152362.2 F90F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr8:22888374 G>T maps to NM_003842.4 I87I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr8:119945326 T>C maps to NM_002546.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:24233222 C>T maps to NM_018647.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr1:12251942 G>T maps to NM_001066.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:12186065 C>T maps to NM_001243.3 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr17:7460465 G>A maps to NM_003809.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MJ-A68H-01A-11D-A307-09 chr19:6669984 C>T maps to NM_003807.3 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:170875362 C>T maps to NM_015028.2 R369R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr3:195609096 C>A maps to NM_001010938.1 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:175063124 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:11362867 C>T maps to NM_005425.4 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KY-01A-11D-A24N-09 chr7:128619087 A>C maps to ENST00000471166 V704V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LT-01A-12D-A21Q-09 chr7:128640524 A>C maps to ENST00000471166 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr1:175372357 C>T maps to NM_003285.2 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr1:175325479 G>A maps to NM_003285.2 G1031G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JL-01A-11D-A36J-09 chr7:5353374 G>A maps to NM_001080495.2 R2383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr17:76047368 A>G maps to NM_001142640.1 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr17:76045613 A>G maps to NM_001142640.1 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I3-01A-11D-A38Z-09 chr6:32014048 G>T maps to ENST00000375244 T3503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:32039914 C>T maps to ENST00000375244 R1614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:32053874 A>G maps to ENST00000375244 L934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB30-01A-11D-A38Z-09 chr6:32064924 G>A maps to ENST00000375244 C235C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DL-01A-11D-A26G-09 chr6:32041700 G>T maps to ENST00000375244 A1468A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:32017937 G>A maps to ENST00000375244 V3092V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:32017936 G>A maps to ENST00000375244 Q3093*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:45806841 C>T maps to NM_025077.3 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr11:1311570 C>T maps to ENST00000382211 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr3:25675376 T>C maps to ENST00000264331 K327K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:25668162 T>C maps to ENST00000264331 Q704Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr20:42635239 A>T maps to ENST00000348077 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LU-01A-11D-A21Q-09 chr16:52473154 C>T maps to ENST00000407228 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr17:7579413 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HU-01A-11D-A38Z-09 chr17:7577497 C>T did not map to a codon.
Sequencing variant TCGA-3B-A9HY-01A-11D-A38Z-09 chr17:7577539 G>A maps to NM_001126112.1 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J1-01A-11D-A21Q-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr17:7576851 C>A did not map to a codon.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr17:7578289 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr17:7578369 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BK-01A-11D-A37C-09 chr17:7578289 C>G did not map to a codon.
Sequencing variant TCGA-DX-A8BV-01A-11D-A37C-09 chr17:7578211 G>A maps to NM_001126112.1 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr17:7578430 G>A maps to NM_001126112.1 Q167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr17:7574002 G>A maps to NM_001126112.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr17:7579414 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr17:7576896 G>A maps to NM_001126112.1 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr17:7579310 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr17:7577045 C>A maps to NM_001126112.1 E298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr17:7577539 G>A maps to NM_001126112.1 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr17:7574033 C>G did not map to a codon.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr17:7577136 C>T maps to NM_001126112.1 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr15:43767782 A>G maps to NM_001141980.1 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:3598952 C>T maps to NM_005427.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr20:62500658 G>A maps to NM_199360.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:144463042 C>T maps to NM_022445.3 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr5:666156 C>T maps to NM_007030.2 K131K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:140093978 C>T maps to NM_001128228.2 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr19:48305589 T>C maps to NM_198479.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:1291581 G>A maps to ENST00000461509 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:26937023 G>A maps to NM_003595.3 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr21:10906903 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr21:10916409 C>T maps to NM_199261.2 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:23556109 G>A maps to NM_013293.3 R70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:123667462 G>A maps to NM_001190945.1 F362F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr14:103369713 G>A maps to NM_145725.2 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:49869410 G>A maps to NM_005879.2 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr3:36874692 G>A maps to NM_014831.2 C2083C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:36875280 G>A maps to NM_014831.2 L1887L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr14:39627486 A>G did not map to a codon.
Sequencing variant TCGA-DX-AB3B-01A-11D-A417-09 chr8:141461085 G>A maps to NM_031466.5 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr6:41121640 C>T maps to NM_178174.2 T77T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:42231057 G>A maps to NM_033502.2 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr12:72866950 C>A maps to NM_013381.2 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr2:12858576 G>C maps to NM_021643.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr7:99490310 C>A maps to NM_033017.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UF-01A-11D-A307-09 chr3:140401654 C>A maps to NM_152616.4 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A3OV-01A-11D-A228-09 chr11:35706845 T>C maps to NM_017583.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr1:155154487 C>T maps to NM_025058.3 G583G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr11:55036762 G>A maps to ENST00000357530 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:248023941 A>G maps to NM_015431.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr5:180622663 C>T maps to NM_203293.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr5:180622492 C>T maps to NM_203293.1 V403V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:32932837 C>T maps to NM_001039111.1 I714I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr4:189063510 G>T maps to NM_178556.3 E204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A75J-01A-11D-A32I-09 chr4:189012787 A>T maps to ENST00000326754 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr4:189026035 A>T maps to ENST00000326754 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2S-01A-11D-A38Z-09 chr5:14487870 C>T maps to NM_007118.2 P2378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N8-01A-11D-A26G-09 chr5:14405991 G>A maps to NM_007118.2 K1584K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr5:14359549 G>T maps to NM_007118.2 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B7-01A-11D-A307-09 chr22:38155237 G>A maps to NM_001039141.2 E2097E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr22:38121163 C>T maps to NM_001039141.2 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr22:38121466 C>T maps to NM_001039141.2 T968T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr2:230683115 C>T maps to ENST00000389044 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:230723647 C>T maps to ENST00000389044 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr7:100470807 G>A maps to NM_003302.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ES-01A-31D-A38Z-09 chr23:54956773 A>G did not map to a codon.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr23:54950978 A>G did not map to a codon.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr8:72975031 A>T did not map to a codon.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr4:122824165 G>T maps to NM_001130698.1 S768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:38266463 G>A maps to NM_003306.1 A302A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EF-01A-11D-A33E-09 chr23:111090650 C>T did not map to a codon.
Sequencing variant TCGA-HB-A3L4-01A-11D-A21Q-09 chr23:111078202 T>G did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:101362322 G>A maps to NM_004621.5 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6B7-01A-11D-A307-09 chr15:31339352 G>A maps to NM_002420.4 N553N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:31294645 G>A maps to NM_002420.4 N1397N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:31319223 G>A maps to NM_002420.4 P1108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr21:45858990 G>A maps to ENST00000397932 K1453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr9:73376618 C>T maps to ENST00000419692 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XY-01A-11D-A37C-09 chr9:73376521 C>A maps to ENST00000419692 E389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:49674906 C>T maps to NM_017636.3 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:49674905 C>T maps to NM_017636.3 C310C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:2432960 G>A maps to ENST00000452833 V839V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:2442421 C>T maps to ENST00000452833 W102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr9:77377881 C>T maps to NM_017662.4 E1235E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L1-01A-11D-A24N-09 chr8:116616854 G>C maps to NM_014112.2 Y447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:142612505 C>T maps to NM_019841.4 T419T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr7:98569419 A>G did not map to a codon.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr7:98602904 C>T maps to ENST00000359863 L3549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:141952290 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:135782742 A>G maps to NM_000368.4 D426D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:99634675 G>A maps to NM_025244.2 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A75J-01A-11D-A32I-09 chr18:72998201 C>T maps to NM_005786.4 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:51870917 G>A maps to NM_173485.5 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:51872432 C>T maps to NM_173485.5 S812S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr19:31769389 G>A maps to NM_020856.2 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:231696970 G>A maps to NM_005999.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr17:79612350 C>T maps to NM_031945.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48P-01A-11D-A307-09 chr11:2334969 G>A maps to NM_139022.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr23:99890553 C>A did not map to a codon.
Sequencing variant TCGA-DX-A48V-01A-11D-A307-09 chr24:9304679 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr24:6115640 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr5:112769636 G>A maps to NM_032028.3 P300P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IE-A3OV-01A-11D-A228-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-FX-A48G-01A-11D-A24N-09 chr15:43044956 C>T maps to ENST00000263802 Q1234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EM-01A-11D-A36J-09 chr5:159492026 C>G maps to NM_003314.1 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:159491940 A>T maps to NM_003314.1 K250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A8JB-01A-23D-A37C-09 chr2:3391676 G>T maps to NM_016030.5 G95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:130485606 C>T maps to NM_144965.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:15909808 C>T maps to NM_017775.2 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:39172546 G>A maps to ENST00000301819 K849K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XZ-01A-11D-A37C-09 chr21:38563713 G>T maps to NM_003316.3 E1702*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr5:94864705 T>C maps to NM_014639.3 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:20768977 C>A did not map to a codon.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr6:80721151 A>T maps to NM_003318.4 A205A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C7-01A-11D-A36J-09 chr9:124801569 A>T maps to NM_001139442.1 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:9876575 C>T maps to NM_001025930.3 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr17:46876979 G>A maps to NM_001130918.1 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:46865261 C>T maps to NM_001130918.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr22:50485695 G>A maps to NM_001080447.1 Y98Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I3-01A-11D-A38Z-09 chr2:179569021 G>T maps to NM_133378.4 G8781G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr2:179641958 G>A maps to NM_133378.4 V1577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48R-01A-11D-A307-09 chr2:179431619 A>G maps to NM_133378.4 D23845D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YZ-01A-12D-A351-09 chr2:179604054 C>A maps to NM_133437.3 V4464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr2:179554617 C>A maps to NM_133378.4 E9346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:179637974 G>A maps to NM_133378.4 I2572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:179485011 G>A maps to NM_133378.4 C12844C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:179458059 C>T maps to NM_133378.4 W17057*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2H-01A-11D-A38Z-09 chr2:179427806 C>T maps to NM_133378.4 V25116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr2:179596645 G>C maps to NM_133378.4 Y4408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr2:179539092 G>T maps to NM_133378.4 I10251I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:179637995 C>T maps to NM_133378.4 W2565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:179463271 G>A maps to NM_133378.4 I16456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:179584941 C>T maps to NM_133378.4 G6565G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:179452028 C>T maps to NM_133378.4 V18735V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:179606001 G>A maps to NM_133437.3 I3815I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:179498050 G>A maps to NM_133378.4 R11749*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr2:179655563 C>T maps to NM_133378.4 Q557Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr2:179594529 C>T maps to NM_133378.4 Q4906Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr2:179417020 G>A maps to NM_133378.4 Y27634Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:63985640 T>A maps to NM_000370.3 K71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr19:54940505 G>A maps to ENST00000391739 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23U-01A-11D-A26G-09 chr7:2696138 C>T maps to NM_025250.2 C407C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr2:132238231 C>T maps to NM_080386.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr2:132240192 G>A maps to NM_080386.2 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr2:220116778 T>C maps to NM_006000.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr10:5435602 G>A maps to NM_024803.2 Y406Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr6:30692041 G>A maps to NM_178014.2 E401E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr6:3155011 G>A maps to NM_001069.2 G141G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BH-01A-11D-A37C-09 chr6:3225062 G>T maps to NM_178012.4 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr19:6495615 G>A maps to NM_006087.2 N298N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr19:6501349 A>G maps to NM_006087.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BF-01A-11D-A307-09 chr10:95172 C>T maps to NM_177987.2 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr6:112393215 G>A maps to NM_016262.4 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A4EJ-01A-11D-A24N-09 chr6:158924150 T>A maps to NM_020245.3 S1152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr6:158915856 C>T maps to NM_020245.3 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr8:15508301 G>A maps to NM_006765.2 E135E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr6:139564103 G>C maps to ENST00000358430 L538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr6:7884717 A>G maps to NM_030810.3 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr3:138037030 T>A maps to ENST00000333911 K76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr2:99944044 C>T maps to NM_005783.3 K87K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:104714904 G>A maps to NM_001093771.1 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WC-01A-12D-A351-09 chr22:19907111 C>A maps to NM_006440.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr19:10463144 G>A maps to NM_003331.4 L1095L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:10467268 A>T maps to NM_003331.4 R864R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-A71Q-01A-12D-A33E-09 chr19:10463609 G>A maps to NM_003331.4 P1064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr15:41854856 G>A maps to NM_006293.3 W174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr9:139975206 C>T maps to NM_207309.2 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr23:47060957 C>T did not map to a codon.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr3:69105347 G>C maps to NM_003968.3 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1L2-01A-22D-A24N-09 chr17:16285593 C>T maps to NM_018955.2 Q125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z2-01A-12D-A36J-09 chr12:125396493 C>T maps to NM_021009.5 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:57327818 G>A maps to NM_004223.3 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:74395723 C>T maps to NM_022066.3 Q478Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr12:109949044 C>T maps to NM_183415.1 D631D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QU-01A-11D-A27P-09 chr12:109948258 C>T maps to NM_183415.1 R618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr12:109921779 T>C maps to NM_183415.1 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BQ-01A-11D-A37C-09 chr7:157013393 C>G maps to NM_014671.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:11346010 C>T maps to NM_013319.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:11345887 C>T maps to NM_013319.2 S239S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BG-01A-12D-A417-09 chr7:138916590 C>A maps to NM_173569.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr23:56592113 C>G did not map to a codon.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr23:56590840 C>A did not map to a codon.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr11:5529534 C>T maps to NM_017481.2 E418E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HL-01A-11D-A387-09 chr6:42583800 G>A maps to NM_015255.2 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BU-01A-11D-A37C-09 chr1:19511666 G>T maps to ENST00000375267 R622R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr1:20517767 C>T maps to NM_152376.3 H238H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr8:30601705 C>T did not map to a codon.
Sequencing variant TCGA-X9-A971-01A-11D-A387-09 chr20:62587647 C>T maps to NM_017859.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr4:141489847 G>T maps to NM_021833.4 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:73717403 C>T maps to NM_003356.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:39515777 G>A maps to NM_003359.3 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr13:96511889 T>A maps to NM_020121.3 P1260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr2:234638179 C>A maps to NM_019093.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UE-01A-11D-A307-09 chr2:234622416 C>T maps to NM_019078.1 D260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr4:69519759 G>A maps to NM_001076.2 D436D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr5:35957293 G>C maps to NM_152404.3 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A6Z4-01A-22D-A33E-09 chr5:35965700 G>A maps to NM_152404.3 F210F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr5:36035964 C>T maps to NM_174914.3 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr5:36039666 C>T maps to NM_174914.3 W329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr4:115585185 T>C maps to NM_003360.3 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr6:34827036 C>T maps to NM_017754.3 G968G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr12:100451838 T>C maps to NM_015054.1 P1072P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A973-01A-11D-A387-09 chr6:150290441 A>T maps to NM_025218.2 K191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HO-01A-11D-A387-09 chr12:132399937 G>A maps to NM_003565.2 E527E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr15:75130778 A>G did not map to a codon.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr21:43531404 G>T maps to NM_173568.3 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr21:43557615 C>T maps to NM_173568.3 F1409F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QU-01A-11D-A27P-09 chr3:124456887 C>T maps to NM_000373.3 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr3:124457072 A>G maps to NM_000373.3 K323K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr15:54590063 G>A maps to ENST00000260323 V1348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr15:54590064 G>T maps to ENST00000260323 E1349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr15:54914550 C>T maps to ENST00000260323 Q2045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DN-01A-12D-A27P-09 chr15:54307903 T>G maps to ENST00000260323 L935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:54305771 T>C maps to ENST00000260323 N224N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr15:54305705 C>T maps to ENST00000260323 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr15:54592541 T>C maps to ENST00000260323 Y1413Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:91479207 C>T maps to NM_018671.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr17:33477088 C>T maps to NM_173167.2 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr5:176301365 C>T maps to NM_133369.2 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr8:35544126 G>A maps to ENST00000416672 R328R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr6:167728837 G>T maps to NM_018974.3 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr11:67766693 G>A maps to NM_030930.2 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr7:1273219 C>G maps to NM_001080461.1 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A42W-01A-11D-A24N-09 chr3:118909893 T>C maps to NM_006952.3 N137N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:118905608 T>A maps to NM_006952.3 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr7:43918206 C>T maps to NM_001077663.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr3:126236445 C>T maps to NM_001165974.1 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2T-01A-11D-A387-09 chr11:17542933 C>T maps to NM_153676.3 K348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:72915946 T>A maps to NM_173477.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr1:216246285 C>T maps to ENST00000366943 S1934S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:215990401 C>T maps to ENST00000366943 K3169K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C2-01A-11D-A36J-09 chr1:216062046 G>T maps to ENST00000366943 T2648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:17362811 G>A maps to NM_031941.3 V569V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr8:11995024 G>A maps to NM_201402.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr8:11995432 G>T maps to NM_201402.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr8:11995495 G>C maps to NM_201402.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BM-01A-11D-A417-09 chr21:17183455 G>T maps to ENST00000285681 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:132161246 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:132160343 T>A did not map to a codon.
Sequencing variant TCGA-DX-A1L3-01A-11D-A24N-09 chr12:109511300 C>G maps to NM_032663.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:219360517 C>T maps to NM_020935.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr3:49373012 G>T maps to NM_003363.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:234442284 G>A maps to NM_018218.2 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr11:11969621 C>T maps to ENST00000399455 S1081S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3LS-01A-11D-A21Q-09 chr1:22073625 T>A maps to NM_032236.5 K309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr15:50835875 T>G maps to ENST00000456636 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr17:5071225 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6B8-01A-11D-A307-09 chr24:14902411 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr13:52603204 C>T maps to NM_021645.5 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr12:101728255 G>A maps to NM_014503.2 L1205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr12:101715332 G>A maps to NM_014503.2 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3M1-01A-11D-A228-09 chr8:117783741 C>T maps to NM_032334.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr4:71555633 C>T maps to NM_020368.2 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr17:30202315 G>A maps to NM_018428.2 I414I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr6:145157026 A>G maps to NM_007124.2 E3259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-N1-A6IA-01A-12D-A32I-09 chr23:47511492 T>G did not map to a codon.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr23:155119267 C>A did not map to a codon.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr1:160394930 G>A maps to NM_020335.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:77242322 C>T maps to NM_014909.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2W-01A-11D-A38Z-09 chr16:77822608 G>A maps to NM_020927.1 E10E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr9:136857267 G>A maps to NM_001134398.1 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AK-01A-21D-A24N-09 chr1:108293736 A>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr1:101196793 C>T maps to NM_001078.3 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:82789386 G>A maps to NM_004385.4 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr23:7811268 G>A did not map to a codon.
Sequencing variant TCGA-DX-A7ET-01A-11D-A36J-09 chr23:8138100 A>T did not map to a codon.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr12:95693941 C>T maps to NM_017599.3 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2O-01A-12D-A38Z-09 chr17:4688743 G>A maps to NM_182566.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr19:53770510 G>T maps to NM_173857.2 I136I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr1:12382757 G>T maps to NM_015378.2 E2624*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr15:41191384 C>T maps to NM_020857.2 Y123Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr16:46696379 A>C maps to NM_018206.4 Y614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr16:69354618 G>A maps to NM_013245.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A2QS-01A-11D-A21Q-09 chr18:61070982 T>C maps to NM_004869.3 K147K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:97313612 C>T maps to NM_003384.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:17830792 C>T maps to NM_003385.4 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr14:74707945 G>A maps to NM_182894.2 K144K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr16:22157663 C>T maps to NM_173615.3 S946S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr2:98804436 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:215279261 C>T maps to NM_001080500.2 F115F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr11:61026599 C>T maps to NM_152718.2 T805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr12:6153546 T>C maps to NM_000552.3 E784E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr12:6078494 C>T maps to NM_000552.3 K2537K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-A68Q-01A-11D-A307-09 chr12:6143931 C>T maps to NM_000552.3 T869T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XQ-01A-11D-A37C-09 chr12:6184681 G>A maps to NM_000552.3 T231T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr12:6078425 G>T maps to NM_000552.3 G2560G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr13:52277757 C>T maps to NM_052950.3 N102N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr4:85701376 G>A maps to NM_014991.4 L1417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr4:85731188 G>A maps to NM_014991.4 S732S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XT-01A-11D-A37C-09 chr4:85758159 C>T maps to NM_014991.4 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr17:9536292 C>T maps to NM_145054.4 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr4:177094498 T>G maps to NM_170710.4 L1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:118499756 C>T maps to NM_006784.2 N840N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HS-A5N7-01A-21D-A26G-09 chr1:118496637 G>A maps to NM_006784.2 R759R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3K7-01A-11D-A21Q-09 chr1:118483748 A>C maps to NM_006784.2 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr23:48932826 C>T did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr3:167248901 C>T did not map to a codon.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr1:241907736 G>T maps to NM_144625.4 E495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr12:122398648 G>A maps to NM_144668.4 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:53809907 G>T maps to NM_182758.2 C1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr15:53994474 C>T maps to NM_182758.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XX-01A-11D-A37C-09 chr17:1631291 G>A maps to NM_001163809.1 A1013A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr17:1630731 C>T maps to NM_001163809.1 Q827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:90255294 G>A maps to NM_020212.1 E200E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB35-01A-21D-A417-09 chr2:160112886 C>T did not map to a codon.
Sequencing variant TCGA-DX-A1KW-01A-22D-A24N-09 chr4:1977055 C>T maps to NM_133335.3 L1184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SI-AA8B-01A-11D-A387-09 chr4:1918631 G>A maps to NM_133335.3 Q265Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr12:1009690 C>T maps to NM_001184985.1 T2426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr23:54275145 C>A did not map to a codon.
Sequencing variant TCGA-DX-A8BT-01A-11D-A37C-09 chr23:54263640 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2F-01A-11D-A387-09 chr23:54319435 A>T did not map to a codon.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr23:54264791 G>T did not map to a codon.
Sequencing variant TCGA-IS-A3K6-01A-11D-A21Q-09 chr17:40936572 G>A maps to NM_032387.4 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3B-01A-11D-A417-09 chr7:116960807 G>A maps to NM_003391.2 C41C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:116918430 C>T maps to NM_003391.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:228210562 C>T maps to ENST00000366753 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VE-01A-11D-A29N-09 chr12:1755192 C>T maps to NM_032642.2 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr22:46345805 G>A maps to NM_058238.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr22:46345806 G>A maps to NM_058238.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EU-01A-22D-A36J-09 chr8:31014957 C>G maps to NM_000553.4 G1298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HP-01A-11D-A387-09 chr12:108589815 C>T maps to ENST00000261400 D69D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPF-01A-11D-A38Z-09 chr5:167855147 T>C did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:39230561 G>T maps to NM_194293.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J0-01A-11D-A21Q-09 chr2:168108281 T>C maps to NM_152381.5 D3460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:167760012 C>T maps to NM_152381.5 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:167760078 G>A maps to NM_152381.5 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:168105326 G>A maps to NM_152381.5 T2475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:6669732 C>T maps to NM_207411.4 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2H-01A-11D-A38Z-09 chr1:28293380 C>A maps to NM_018053.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr23:100182985 T>G did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:100177792 G>A did not map to a codon.
Sequencing variant TCGA-KD-A5QT-01A-11D-A27P-09 chr23:128894540 T>G did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr13:21373399 G>A maps to NM_022459.4 F742F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A6FX-01A-11D-A32I-09 chr16:28113176 C>G maps to NM_015171.2 L1012L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr14:104165289 G>A maps to NM_005432.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr22:42018076 C>T maps to NM_001469.3 N23N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:17211524 C>T maps to NM_022166.3 S845S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr16:17451889 C>T maps to NM_022166.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr12:42555464 T>C maps to NM_001190979.1 E109E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AK-01A-21D-A24N-09 chr11:101985017 C>G maps to NM_001130145.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr11:66055129 G>A maps to ENST00000376904 Y126Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr4:44626622 T>A maps to NM_182592.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I1-01A-11D-A38Z-09 chr14:75265722 C>A maps to NM_019589.2 L1241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr14:75266068 C>T maps to NM_019589.2 R1357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RV-01A-11D-A32I-09 chr10:27403537 T>C did not map to a codon.
Sequencing variant TCGA-K1-A6RU-01A-11D-A32I-09 chr1:38269623 C>A maps to NM_024640.3 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7W8-01A-21D-A351-09 chr4:69202907 C>T maps to NM_001031732.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr8:64100287 G>A maps to ENST00000339066 E572E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M6-01A-11D-A21Q-09 chr20:43532647 A>G maps to NM_139323.2 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XQ-01A-11D-A37C-09 chr7:75958929 G>A maps to NM_012479.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KD-A5QS-01A-11D-A27P-09 chr14:100705950 G>T maps to NM_003403.3 E124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:21875571 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:21875570 C>T did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:100350370 C>T maps to ENST00000349350 P881P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr2:98340858 C>T maps to NM_001079.3 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A5W3-01A-11D-A29N-09 chr3:167031768 A>G maps to ENST00000307529 N470N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:167068245 T>A maps to ENST00000307529 K164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr23:2408603 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:101375071 G>A maps to NM_014415.3 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:114069529 G>A maps to NM_001164342.1 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VE-01A-11D-A29N-09 chr11:62520109 G>A maps to NM_024784.3 Q393*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:36207191 C>G maps to NM_014383.1 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:59025633 A>C maps to NM_032792.2 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23Y-01A-11D-A27P-09 chr20:62384158 C>T maps to NM_025224.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr1:203809456 G>T maps to NM_014827.4 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KF-A41W-01A-11D-A24N-09 chr23:64722227 T>A did not map to a codon.
Sequencing variant TCGA-DX-A7EL-01A-12D-A36J-09 chr2:187370519 T>C maps to NM_018471.2 D306D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr16:88643764 C>T maps to ENST00000452588 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-K1-A6RT-01A-32D-A33E-09 chr16:88643647 C>T maps to ENST00000452588 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9I3-01A-11D-A38Z-09 chr8:144621416 C>T maps to NM_015117.2 Q40Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VH-01A-11D-A37C-09 chr23:64140080 G>T did not map to a codon.
Sequencing variant TCGA-IE-A6BZ-01A-11D-A307-09 chr23:117959329 A>T did not map to a codon.
Sequencing variant TCGA-VT-A80J-01A-11D-A36J-09 chr23:117960019 C>T did not map to a codon.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr23:73524387 G>C did not map to a codon.
Sequencing variant TCGA-DX-A3U9-01A-11D-A307-09 chr20:279423 C>T maps to NM_033089.6 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:77913317 G>A did not map to a codon.
Sequencing variant TCGA-DX-A6BA-01A-11D-A307-09 chr9:88924911 A>G maps to NM_024617.3 L1133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A5YA-01A-11D-A29N-09 chr7:100014753 T>C maps to NM_017984.3 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB37-01A-11D-A417-09 chr2:207175935 G>T maps to NM_020923.1 S2228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BO-01A-11D-A417-09 chr16:67432539 G>A maps to NM_013304.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr5:843754 G>A maps to NM_024786.2 L196L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-QQ-A8VH-01A-11D-A37C-09. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DX-A3LY-01B-11D-A27P-09 chr23:74641737 C>G did not map to a codon.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr23:74649795 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr3:113675254 C>T maps to NM_173570.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr3:44968198 C>T maps to NM_016598.2 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:44974450 C>T maps to NM_016598.2 E214E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr7:6621841 A>G maps to NM_018106.3 V110V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr10:114194075 G>A maps to NM_022494.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A8JB-01A-23D-A37C-09 chr10:114194137 G>A maps to NM_022494.1 Q274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:85010005 G>A maps to NM_001145548.1 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DN-01A-12D-A27P-09 chr8:82626244 G>A maps to NM_024699.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr16:72827757 T>A maps to NM_006885.3 G2941G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr16:72832404 C>T maps to NM_006885.3 P1392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BB-01A-12D-A32I-09 chr8:77768254 C>G maps to NM_024721.4 S3033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr8:77766188 A>G maps to NM_024721.4 Q2344Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IW-A3M5-01A-22D-A21Q-09 chr8:77766737 G>A maps to NM_024721.4 P2527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C4-01A-11D-A36J-09 chr6:29640429 A>G maps to NM_001109809.2 S486S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BV-01A-11D-A37C-09 chr5:32379259 G>A maps to NM_016107.3 L932L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr19:3825348 C>T maps to NM_015174.1 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr23:24227113 A>C did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr23:24229431 G>A did not map to a codon.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr23:24197841 C>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr14:73437766 G>A maps to NM_021260.2 L719L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr15:41105990 C>T maps to NM_001077268.1 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2Z-01A-11D-A387-09 chr4:2307169 G>A maps to NM_020972.2 D299D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VA-01A-12D-A32I-09 chr4:2321943 G>A maps to NM_020972.2 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr1:52704474 C>T maps to NM_004799.2 F462F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HQ-01A-11D-A387-09 chr8:123965960 C>T maps to NM_014943.3 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2IZ-01A-11D-A21Q-09 chr20:39833133 G>A maps to NM_015035.3 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr13:100635184 G>A maps to NM_007129.2 V289V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:136652048 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr19:57646927 G>T maps to NM_052882.1 A259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:25255457 G>A maps to NM_001012981.4 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr23:101159270 G>T did not map to a codon.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr23:101153191 C>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:101139136 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr10:81070907 G>A maps to NM_020338.3 Q1021Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:44802945 G>A maps to NM_031449.3 L598L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8Y0-01A-11D-A417-09 chr1:35580502 C>T maps to NM_024772.3 I1024I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2X-01A-11D-A387-09 chr23:70469940 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:70469918 G>A did not map to a codon.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr23:70469917 G>A did not map to a codon.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr23:70462038 G>A did not map to a codon.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr23:70464191 G>T did not map to a codon.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr10:226044 T>C maps to NM_006624.4 I31I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-UE-A6QU-01A-12D-A32I-09 chr12:133733334 G>A maps to NM_015394.4 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A23R-01A-11D-A26G-09 chr19:21910054 G>A maps to NM_173531.3 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr7:6732293 C>T maps to ENST00000330442 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB35-01A-21D-A417-09 chr4:367649 G>A maps to NM_003441.2 *475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB35-01A-21D-A417-09 chr4:367635 G>A maps to NM_003441.2 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:28056767 C>T maps to NM_003447.3 F326F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:57932770 T>G maps to NM_006959.2 P637P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3TO-01A-11D-A228-09 chr19:9491684 T>A maps to NM_001172651.1 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2F-01A-11D-A387-09 chr23:47842771 G>T did not map to a codon.
Sequencing variant TCGA-DX-AB2L-01A-32D-A417-09 chr6:28121012 G>T maps to NM_006298.2 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr16:3191239 C>T maps to NM_001134655.1 T424T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3U7-01A-11D-A29N-09 chr11:6977272 T>A maps to NM_013250.2 Y355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:44470187 C>T maps to NM_013359.2 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:44536291 T>C maps to NM_001129996.1 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr19:44622635 G>T maps to NM_013362.2 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A2J1-01A-11D-A21Q-09 chr19:44934382 C>T maps to NM_014518.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7ET-01A-11D-A36J-09 chr19:44933793 G>A maps to NM_014518.2 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:44512952 C>T maps to NM_006300.3 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:5009421 T>C maps to NM_014519.2 S344S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:44778225 G>A maps to NM_181756.1 Q471Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:44660467 G>A maps to NM_006630.2 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:44660468 G>A maps to NM_006630.2 W100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr19:44653050 G>A did not map to a codon.
Sequencing variant TCGA-HB-A43Z-01A-11D-A24N-09 chr18:74589966 C>G maps to NM_007345.3 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr10:38241129 C>T maps to NM_145011.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:20002338 C>T maps to ENST00000427401 Q31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AATS-01A-12D-A417-09 chr19:22271886 C>A maps to NM_033468.2 Y445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-A9VC-01A-11D-A37C-09 chr19:57724347 G>T maps to NM_003417.4 *628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KU-01A-32D-A24N-09 chr16:31927604 C>A maps to NM_003414.4 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr19:58723008 C>T maps to NM_133502.1 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-SG-A849-01A-11D-A351-09 chr15:56999298 G>A maps to NM_017661.2 D3D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr1:200378098 C>T maps to NM_012482.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JL-01A-11D-A36J-09 chr19:44892205 C>A maps to NM_152354.3 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PT-A8TR-01A-11D-A37C-09 chr19:44892205 C>A maps to NM_152354.3 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr17:16470889 A>G maps to NM_020653.2 F52F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KX-01A-22D-A24N-09 chr21:43412113 G>T maps to NM_020727.4 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YQ-01A-12D-A33E-09 chr5:150282890 A>G maps to NM_001172831.1 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:58030804 C>T maps to NM_020807.1 E455E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr19:58966802 C>T maps to NM_207395.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr20:45131080 C>T maps to NM_018102.3 R299R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr20:44582451 G>A maps to NM_022095.3 Q860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VF-01A-11D-A29N-09 chr20:25657392 C>T maps to NM_015655.2 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3R-A8YX-01A-11D-A37C-09 chr20:32346564 T>C maps to ENST00000375200 C327C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr19:37367975 C>T maps to NM_003419.3 R82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X9-A971-01A-11D-A387-09 chr5:178310889 C>T maps to NM_058230.2 S479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5V9-01A-11D-A32I-09 chr19:7584580 C>T maps to NM_018083.4 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr5:71756677 T>A maps to NM_152625.1 K216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:180348038 G>A maps to NM_152520.4 C210C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr3:21706428 G>A maps to NM_024697.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BX-01A-11D-A37C-09 chr7:148851393 C>T maps to NM_170686.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr19:44378125 G>A maps to ENST00000324394 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FX-A3RE-01A-11D-A228-09 chr19:58084053 T>C maps to NM_017879.1 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:44496723 G>A maps to NM_181489.5 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr6:57017091 C>T maps to NM_001031623.2 F942F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IS-A3KA-01A-11D-A21Q-09 chr6:57017070 G>A maps to NM_001031623.2 L935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6BK-01A-11D-A307-09 chr7:149461817 G>C maps to NM_207336.1 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr7:149462897 C>A maps to NM_207336.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr9:114296582 G>A maps to NM_133464.2 W224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr19:20296805 C>G maps to NM_052852.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr19:20296830 C>T maps to NM_052852.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-WK-A8XO-01A-11D-A37C-09 chr19:20296823 C>T maps to NM_052852.2 I62I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr3:44762542 C>T maps to NM_033210.4 F78F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr4:10447631 C>T maps to NM_053042.2 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr18:22806846 G>A maps to NM_015461.2 S345S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MB-A8JL-01A-11D-A36J-09 chr18:22805727 G>T maps to NM_015461.2 T718T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HT-01A-11D-A38Z-09 chr19:42730291 C>T maps to NM_133444.1 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:52919607 C>T maps to NM_032423.2 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr19:37047080 G>A maps to NM_001145649.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:58115664 G>A maps to NM_020880.3 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VB-01A-11D-A36J-09 chr19:30935047 C>T maps to NM_014717.1 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-LI-A9QH-01A-11D-A37C-09 chr19:36685965 C>T maps to ENST00000355114 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A7WD-01A-21D-A351-09 chr19:37975445 C>A maps to NM_144694.1 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:125989595 G>A maps to NM_152412.2 E362E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr19:53270246 G>A maps to NM_198457.2 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HS-01A-11D-A38Z-09 chr12:133502015 C>A maps to NM_001164715.1 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HR-01A-11D-A387-09 chr19:38189645 T>C maps to NM_032689.4 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HB-A2OT-01A-11D-A21Q-09 chr5:124079848 G>A maps to NM_020747.2 N278N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr19:52869686 C>G maps to NM_001161425.1 V352V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr9:116795003 C>T maps to ENST00000374126 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr8:144733163 C>T maps to NM_014789.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:55994116 C>T maps to NM_033113.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr16:30795099 G>A maps to NM_001080417.1 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HV-01A-11D-A38Z-09 chr23:47920219 G>T did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:47918036 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr2:71650321 T>C maps to NM_014497.3 S1226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-RN-AAAQ-01A-21D-A38Z-09 chr2:71651101 A>C maps to NM_014497.3 I1486I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A1KZ-01A-11D-A24N-09 chr1:40929110 G>A maps to NM_023070.2 R485R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr1:40928207 C>T maps to NM_023070.2 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6Z0-01A-13D-A36J-09 chr23:22291372 G>A did not map to a codon.
Sequencing variant TCGA-DX-A8BZ-01A-11D-A37C-09 chr16:31092309 C>T maps to NM_014699.3 D1555D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HX-01A-11D-A38Z-09 chr9:40772811 T>C maps to NM_033160.5 T821T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YR-01A-33D-A351-09 chr19:53668215 A>G maps to NM_024733.3 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VC-01A-31D-A32I-09 chr19:58238815 C>T maps to ENST00000335820 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB32-01A-11D-A417-09 chr1:249142624 G>A maps to NM_024836.1 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PC-A5DO-01A-11D-A26G-09 chr19:22363459 A>G maps to NM_001001411.2 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-JV-A5VF-01A-11D-A29N-09 chr7:63727245 A>C maps to NM_153363.2 *412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Z4-AAPG-01A-11D-A38Z-09 chr8:81571894 C>T maps to NM_001033723.2 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB3B-01A-11D-A417-09 chr8:144776687 C>T maps to NM_173831.3 H368H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BR-01A-11D-A417-09 chr23:84520143 G>A did not map to a codon.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr7:57529219 C>G maps to NM_001159279.1 L351L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-X6-A8C6-01A-11D-A36J-09 chr7:57522797 A>G maps to NM_001159279.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A3UB-01A-11D-A307-09 chr6:35255450 C>T maps to NM_003427.3 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:12087854 C>T maps to NM_001012753.1 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr16:30567120 G>A maps to NM_033410.3 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr7:148767610 G>A maps to NM_152411.3 I751I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IE-A3OV-01A-11D-A228-09 chr19:37309349 G>A maps to NM_206894.2 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr19:12734575 T>G maps to NM_153358.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BL-01A-11D-A417-09 chr23:47775957 A>G did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr23:47705687 C>T did not map to a codon.
Sequencing variant TCGA-WP-A9GB-01A-11D-A37C-09 chr23:47774882 G>C did not map to a codon.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:57769469 C>T maps to NM_178457.1 S1132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr20:57828126 C>T maps to NM_178457.1 T1374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:12186141 G>A maps to NM_001136501.1 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A7EQ-01A-11D-A387-09 chr7:149545353 C>T maps to NM_001099220.1 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:149547267 C>T maps to NM_001099220.1 L320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr7:149558297 C>T maps to NM_001099220.1 I683I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr19:20228656 G>A maps to NM_007138.1 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BS-01A-11D-A37C-09 chr19:22942485 T>A did not map to a codon.
Sequencing variant TCGA-HB-A3YV-01A-11D-A24N-09 chr11:64884314 G>A maps to NM_014205.2 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BP-01A-11D-A37C-09 chr22:29446775 C>T maps to NM_032173.2 G769G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A6YX-01A-11D-A417-09 chr19:5456438 C>T maps to NM_181710.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48O-01A-11D-A307-09 chr1:238048787 T>G maps to NM_021186.3 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr3:102187921 C>T maps to NM_175056.1 V308V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr2:136029337 C>T maps to NM_032143.2 Q402Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr2:135975069 G>A maps to NM_032143.2 I820I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A8BJ-01A-11D-A417-09 chr19:58549416 G>A maps to NM_182572.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2V-01A-11D-A417-09 chr19:58549272 C>T maps to NM_182572.3 D23D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A8VG-01A-11D-A37C-09 chr19:58596420 G>A maps to NM_001145542.1 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QQ-A5VD-01A-21D-A32I-09 chr15:85165024 C>T maps to NM_181877.3 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr1:33956655 C>T maps to NM_145238.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-A48U-01A-11D-A307-09 chr7:99654809 G>T maps to NM_145914.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IF-A4AJ-01A-11D-A24N-09 chr15:43656521 C>T maps to NM_152455.3 Q427Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QC-A7B5-01A-11D-A33E-09 chr15:43658599 C>T maps to NM_152455.3 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-VT-A80G-01A-11D-A36J-09 chr19:56701297 G>A maps to NM_001080456.2 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DX-AB2E-01A-11D-A38Z-09 chr20:44506222 T>C maps to NM_080752.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-3B-A9HJ-01A-11D-A387-09 chr19:13919957 G>A maps to NM_023072.2 Q312Q. Only missense variants will be evaluated by CHASM.
