5022 NP_001070868 H778R not found in SNVbox database
5726 NP_705833 E584K not found in SNVbox database
6515 NP_705833 G776S not found in SNVbox database
9368 NP_705833 I714K not found in SNVbox database
209 NP_001070868 K360Q not found in SNVbox database
438 NP_001070868 E650G not found in SNVbox database
877 NP_705833 S703A not found in SNVbox database
1278 NP_705833 E822Q not found in SNVbox database
1335 NP_001070868 Y730H not found in SNVbox database
1550 NP_705833 G713R not found in SNVbox database
3490 NP_001070868 I713K not found in SNVbox database
4606 NP_001070868 F749L not found in SNVbox database
4832 NP_001070868 R224K not found in SNVbox database
4849 NP_001070868 Q386P not found in SNVbox database
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:62978868 G>T maps to NM_015059.2 V329V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:71293805 A>T maps to ENST00000376535 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:47845306 C>T maps to NM_017895.7 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:103090669 T>G maps to NM_001080463.1 L2953L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:61034969 C>T maps to NM_152718.2 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr7:20685386 C>T maps to NM_001163941.1 I229I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr15:33990172 C>T maps to NM_001036.3 N2075N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:16257093 C>T maps to NM_015001.2 S1453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:26407899 A>T maps to NM_007048.5 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:66259192 C>T maps to NM_005700.3 Y318Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:54635835 A>G did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr7:84694821 A>G maps to NM_152754.2 D212D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr12:57962798 C>T maps to NM_004984.2 N256N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr18:23759095 T>C did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:20370790 C>T maps to NM_174924.1 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:56043917 C>T maps to NM_001004745.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr19:34887246 A>G maps to NM_000175.3 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr2:177034057 C>T maps to NM_006898.4 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr9:101748354 C>T maps to NM_001855.3 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr16:18866182 T>C maps to ENST00000389467 L1426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr20:56099192 C>T maps to ENST00000423479 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:17958925 C>T maps to NM_018125.3 L565L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr8:27605730 G>C maps to NM_018246.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:138643656 A>C maps to ENST00000394800 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:94980699 A>G did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr1:158576524 C>T maps to NM_001004478.1 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr11:65123662 A>G maps to NM_145719.2 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:117663707 C>A did not map to a codon.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr17:54969321 G>A maps to NM_005082.4 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr6:42975222 C>T maps to NM_006245.2 I235I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5737-01A-11D-1576-08 chr5:21755849 G>A maps to NM_004061.3 Q579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr22:33260925 T>C maps to NM_003490.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr1:203316789 C>T maps to NM_002023.3 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr1:203819751 G>A maps to NM_014827.4 V683V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr4:54424151 C>A did not map to a codon.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr17:18137335 C>T maps to NM_004140.3 D187D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr19:53270591 A>C maps to NM_198457.2 Y139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr19:51219978 G>A maps to ENST00000391814 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chrX:84561265 G>T maps to ENST00000373145 S413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr21:16338591 G>T maps to NM_003489.3 S641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chr22:30688747 G>A maps to ENST00000403477 C388C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5738-01A-11D-1576-08 chrX:151869831 C>T maps to NM_005363.2 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:128408803 G>A maps to NM_005291.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:3990603 G>A maps to NM_152744.3 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr15:65685845 G>A maps to NM_020962.1 R580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr17:40474447 A>G maps to NM_139276.2 A651A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:68906684 T>C did not map to a codon.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr13:47269053 G>T maps to NM_001164211.1 E383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:201846108 G>A maps to NM_173822.3 Q493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:89531567 T>C maps to NM_020358.2 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:9595848 C>G maps to NM_016207.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr2:68882251 G>T maps to NM_138964.2 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr7:141635652 T>C maps to NM_013252.2 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr8:139788237 G>A maps to NM_152888.1 R592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr11:62038407 G>C maps to NM_002411.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:235950606 A>G maps to NM_000081.2 N1585N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5739-01A-11D-1576-08 chr1:23650123 T>C maps to ENST00000414299 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr15:101938638 A>C maps to NM_002570.3 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr12:50349300 G>A maps to NM_000486.5 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr1:107961229 G>A maps to NM_001113228.1 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr12:125398089 C>T maps to NM_021009.5 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr13:25376710 T>A did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr1:236760201 C>G maps to NM_018072.5 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr6:76604977 G>A did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr8:103664290 T>A did not map to a codon.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr17:26680001 G>A maps to NM_015584.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr6:52285246 G>A maps to NM_018100.3 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr20:30584458 C>T maps to NM_001011718.1 R313R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5740-01A-11D-1576-08 chr20:30904101 C>T maps to NM_004798.3 R496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chrX:70471026 C>A did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:101946633 G>T maps to NM_032930.2 E156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:5905956 C>T maps to NM_001005165.1 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:124705462 G>A maps to NM_001003954.1 R247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr1:24676594 C>G maps to NM_021180.3 Y564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:54791831 A>T maps to NM_170587.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr1:39798823 A>G maps to ENST00000289893 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr11:88781127 G>A did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr17:900588 C>A maps to NM_013337.2 C69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr10:118441314 G>T maps to NM_025015.2 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr19:54760065 G>T maps to NM_001081442.1 T165T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr18:14757888 C>G maps to NM_001145029.1 V231V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr10:61827717 G>A maps to NM_020987.2 A4098A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr8:145150821 G>A maps to NM_001916.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr4:20751287 G>A maps to ENST00000382152 F142F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr1:67206952 A>T did not map to a codon.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr14:102474612 C>A maps to NM_001376.4 S1972S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr19:3600347 C>T maps to NM_201636.2 W95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr12:81647349 T>C maps to NM_024560.2 A632A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chr2:127958779 G>T maps to NM_001001665.3 G102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5741-01A-11D-1576-08 chrX:9912814 C>T maps to NM_001649.2 P1482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5743-01A-21D-1576-08 chr11:43876381 C>A maps to NM_016142.2 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:17950418 T>A maps to NM_000215.3 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:58565059 C>A maps to NM_182572.3 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr1:197313414 A>G maps to NM_201253.2 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:123893784 C>T maps to NM_001001953.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr11:123909642 G>A maps to NM_001004463.1 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:51102012 G>A maps to NM_004947.4 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr19:50248601 C>T maps to NM_021733.1 V348V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chrX:70280883 C>A maps to NM_013346.2 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr3:51101985 G>A maps to NM_004947.4 E141E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr12:101876610 A>G maps to ENST00000299272 Q84Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr17:26961607 A>G maps to NM_014680.2 P999P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5744-01A-11D-1576-08 chr1:181725166 C>T maps to ENST00000357570 Y1355Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr17:10430103 G>A maps to NM_017534.5 N1333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr16:27782956 G>A maps to NM_015202.2 P1394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr16:11785488 G>A maps to ENST00000356957 F546F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr14:105414188 A>T maps to NM_138420.2 I2533I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CH-5745-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr2:136630396 C>A maps to NM_005915.4 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr3:197497067 G>A maps to NM_032288.6 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr19:7964265 A>C maps to NM_025061.3 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr8:144995012 G>T maps to NM_201380.2 I3129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr17:37830250 G>A maps to NM_033419.3 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5745-01A-11D-1576-08 chr6:3850734 C>T maps to NM_012135.1 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr10:27436414 C>T did not map to a codon.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr22:24622216 C>A maps to NM_001099781.1 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr5:133914475 G>A maps to ENST00000448712 G674G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr1:26691328 C>A maps to ENST00000436292 L236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5746-01A-11D-1576-08 chr19:11558390 G>A maps to ENST00000436195 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr16:3786755 A>G maps to NM_004380.2 H1485H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr12:7177942 C>T maps to NM_001734.3 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr6:87725480 C>A maps to NM_000865.2 I143I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:59282921 C>T maps to NM_001004711.1 C179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr2:193056698 T>C maps to NM_016192.2 E63E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr1:55457538 C>T maps to NM_182532.1 Y132Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr4:8235131 G>A maps to NM_018986.3 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr17:33462275 C>T maps to NM_018096.3 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr11:108032026 A>G maps to NM_002519.2 S1262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr4:48994015 T>C maps to NM_025087.2 Y140Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr13:39262557 T>C maps to NM_207361.4 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr9:94495689 C>T maps to NM_004560.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr22:44892838 G>A maps to NM_032287.2 R200*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-CH-5748-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr20:4770304 G>A maps to NM_014737.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:100971251 G>A maps to NM_018421.3 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr20:61525226 G>A maps to NM_033081.2 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr2:79349166 C>T maps to NM_002909.4 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chrX:140985037 C>T maps to NM_138702.1 F498F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr6:28227391 C>T maps to NM_001007531.1 Y81Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:88650292 A>G maps to ENST00000376023 A344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr6:160237000 T>C maps to NM_173516.1 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr17:6673969 T>C maps to NM_017523.2 C172C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:19041571 T>C maps to NM_024847.3 F246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr1:108247661 A>G maps to NM_006113.4 Y508Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr16:31499067 G>A maps to ENST00000431354 W291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr8:113657356 A>T maps to NM_198123.1 V1097V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr7:27565970 G>A maps to NM_152740.3 D291D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:131531125 C>A maps to NM_001142599.1 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr12:32764088 T>C maps to NM_139241.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr13:21557699 G>A maps to NM_014572.2 A715A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:149755318 C>T maps to ENST00000451292 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr10:51584845 G>A maps to NM_001145260.1 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr9:116858373 C>A maps to ENST00000259410 L279L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr17:1840947 G>A maps to NM_178568.2 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr5:41382447 G>A maps to NM_001005473.2 R98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5750-01A-11D-1576-08 chr19:10335296 A>T maps to NM_004230.3 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr5:140865885 C>T maps to NM_018928.2 N382N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr11:65793238 G>A maps to NM_053054.3 H204H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chrX:112058795 C>T maps to NM_001113490.1 Q394Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr14:66208992 G>C maps to NM_178155.1 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr12:22035726 G>A maps to NM_005691.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr6:25472739 G>T maps to NM_017640.5 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr6:33377449 C>T maps to NM_002263.3 Q669*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr11:28058050 A>G maps to NM_031217.3 I703I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr8:21768189 C>T maps to NM_003974.2 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5751-01A-11D-1576-08 chr1:115005787 G>A maps to NM_015906.3 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr8:53045684 G>A maps to NM_014682.2 C792C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:43926837 C>T maps to ENST00000372754 S507S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:62178594 G>A maps to NM_080823.2 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr2:131096731 G>C maps to NM_032357.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:177022270 C>T maps to NM_017510.4 R188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr22:39421245 C>T maps to NM_152426.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:27755319 G>A maps to NM_006990.2 C27C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr5:9629678 G>A maps to NM_019599.2 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr3:176755960 C>G did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:158612200 C>T maps to NM_003126.2 K1579K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr6:129601259 C>T maps to NM_000426.3 C835C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr16:84906611 C>T maps to NM_031476.3 C332C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr15:89074915 G>A maps to NM_017996.3 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr6:52400645 T>A did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr20:34389528 T>G did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr10:17032434 C>T maps to NM_001081.3 E1416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr2:171862700 A>G maps to ENST00000360843 G641G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr13:27649443 T>A maps to NM_182488.3 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr19:58863781 C>T maps to NM_130786.3 E160E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr3:45761022 A>G maps to NM_014016.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr14:102891313 A>T did not map to a codon.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr11:61111397 G>A maps to NM_015533.3 R351R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr7:87082327 A>G maps to NM_018849.2 A156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5752-01A-11D-1576-08 chr1:89587610 G>C maps to NM_004120.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr3:50879109 G>A maps to NM_004947.4 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr9:139651557 C>T maps to ENST00000371689 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr17:60654068 G>A did not map to a codon.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr8:113277664 C>T maps to NM_198123.1 W3221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr8:11667247 G>A maps to NM_004462.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr15:33835895 C>T maps to NM_001036.3 D240D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr7:98460808 G>A maps to NM_001134450.1 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr16:3190969 G>A maps to NM_001134655.1 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr16:2827128 C>T did not map to a codon.
Sequencing variant TCGA-CH-5753-01A-11D-1576-08 chr15:43896962 G>A maps to NM_153700.2 R1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:38618224 G>A maps to NM_001099404.1 N1146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:5948525 G>A maps to NM_032807.3 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:100775171 G>A maps to NM_000602.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:34072055 C>A maps to NM_139285.2 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr9:129595972 C>T maps to NM_014007.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:74421956 G>T maps to NM_015424.3 I123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:67173157 G>A maps to NM_198517.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:38172079 A>G maps to NM_000759.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr17:26851603 C>T maps to NM_003593.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr15:35185965 G>C maps to NM_014691.2 G823G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chrX:47039693 C>G maps to NM_005676.3 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:2419085 C>A maps to NM_014638.2 Y388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr6:56341000 T>C maps to ENST00000361203 K7059K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr14:71514562 G>A maps to NM_014982.2 L1400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr4:162577599 A>G maps to NM_020116.3 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr2:220348802 C>T maps to NM_005876.4 P2206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:99474213 G>T maps to NM_001005276.1 S148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:100775169 T>C maps to NM_000602.3 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:30935326 C>T maps to NM_014717.1 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr14:45639924 T>G maps to NM_020937.2 S712S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr8:121554094 T>A maps to NM_021021.3 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:50979131 G>A maps to ENST00000391816 D106D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr19:9071590 G>T maps to NM_024690.2 P5285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:194126842 C>T maps to NM_024524.3 E1162E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr11:92570899 C>T maps to ENST00000298047 V3432V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr22:46658214 G>T maps to NM_006071.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr16:31498983 C>G maps to ENST00000431354 Y263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr3:36524553 C>T maps to NM_003149.1 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:179638342 T>C maps to ENST00000444136 N888N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr7:135106937 A>C maps to NM_001190850.1 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:92262993 A>T maps to NM_003243.4 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr1:10231329 G>A maps to NM_001105562.2 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:99655148 G>A maps to NM_018058.4 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5754-01A-11D-1576-08 chr10:48390796 C>A maps to NM_002900.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr6:118598701 G>A maps to NM_001029858.3 W280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr16:47189689 C>A did not map to a codon.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr15:45695157 G>A maps to NM_024063.2 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:212251656 C>A maps to NM_005235.2 V1134V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:184075850 G>T maps to NM_004366.4 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:64065642 C>T maps to ENST00000422670 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:36874131 C>T maps to NM_014831.2 L2270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:50147120 G>A maps to NM_005778.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr9:123805396 C>T maps to NM_001735.2 V102V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86663023 G>A maps to NM_012193.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:141754595 C>T maps to ENST00000475668 L1068L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr1:234556447 C>T maps to NM_005646.3 Q1185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:227729678 G>A maps to NM_001167608.1 W90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr4:57272693 G>A maps to NM_002703.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:120381667 C>A maps to NM_012281.2 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr16:46943651 C>T maps to NM_133443.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:9482198 G>A maps to ENST00000407969 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr3:2613234 C>A maps to NM_175607.1 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr15:91549290 T>A did not map to a codon.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86662612 G>A maps to NM_012193.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr11:86662879 G>A maps to NM_012193.2 F306F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr17:46622153 C>G maps to NM_002145.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr2:242066483 C>A maps to ENST00000358649 E616*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chrX:32380925 T>C maps to ENST00000357033 S1768S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chrX:5821236 G>C maps to ENST00000381093 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr7:87476438 T>A did not map to a codon.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr8:101589257 G>A maps to NM_152628.3 Q406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chrX:153940642 G>C maps to NM_001081573.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr9:95784667 A>C maps to NM_033086.2 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr14:21250157 C>T maps to NM_005615.4 N100N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:128399722 C>A maps to NM_017980.4 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr10:74034534 G>A maps to NM_019058.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr11:77911273 C>T maps to NM_020798.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:160710868 A>T did not map to a codon.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:11214314 T>A maps to ENST00000422992 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr11:66192367 C>T maps to NM_178864.3 D669D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr10:101120670 G>A maps to NM_020348.2 T599T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:10292481 C>T maps to ENST00000377086 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr18:40853619 T>A maps to NM_020783.3 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:116457670 C>T maps to NM_015335.4 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:110217412 C>G maps to ENST00000369830 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr7:43659291 C>T maps to NM_004760.2 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:133428222 C>T maps to NM_001161344.1 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr1:45484151 G>A maps to NM_020883.1 L1178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr2:209302259 A>T did not map to a codon.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr12:18237548 C>A maps to NM_024730.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr15:65502036 C>A maps to NM_003613.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr6:47650244 G>A maps to NM_153839.6 K582K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr1:240977012 C>A maps to ENST00000407727 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr22:21322167 G>A did not map to a codon.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr4:122075726 A>G maps to ENST00000509841 C234C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr2:183846058 A>G maps to NM_205842.1 H424H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr12:116446660 C>A maps to NM_015335.4 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr9:131503067 C>T maps to NM_006336.2 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr11:5529390 T>C maps to NM_017481.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr12:133197606 T>C maps to NM_170683.2 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5763-01A-11D-1576-08 chr17:48193047 C>T maps to NM_174920.2 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr7:91631336 A>G maps to NM_005751.4 L702L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:16257157 C>T maps to NM_015001.2 R1475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr12:64173823 C>T maps to NM_014254.1 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr3:183547481 G>A maps to NM_018622.5 Y348Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr5:137485405 G>A maps to NM_139199.1 G1067G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr2:209190766 C>T maps to NM_015040.3 R1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr5:5303542 G>A maps to NM_139056.2 Q984Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr1:51826840 A>G did not map to a codon.
Sequencing variant TCGA-CH-5764-01A-21D-1576-08 chr22:19467484 C>A did not map to a codon.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:157504476 T>C maps to NM_031281.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr17:39881380 G>A maps to ENST00000310778 R530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:56539872 A>G maps to NM_153447.4 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:23828654 C>T maps to NM_005864.2 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr14:26917260 T>C maps to ENST00000449198 G493G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr11:59608633 A>G maps to NM_005142.2 S225S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:216052410 G>A maps to ENST00000366943 N2751N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr12:122825727 C>A maps to ENST00000302528 E675*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr8:131792812 G>A maps to NM_001115.2 A1193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr2:179477936 A>G maps to NM_133378.4 P13965P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr1:247695756 G>A maps to NM_198074.4 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr19:44564708 G>A maps to NM_013361.4 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr2:191922751 G>A maps to NM_003151.2 R400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr13:29599665 C>T maps to NM_001033602.2 S287S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr16:2506606 C>T maps to NM_001761.2 C649C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5765-01A-11D-1576-08 chr4:122063931 C>A did not map to a codon.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr9:138651632 G>A maps to ENST00000298480 T321T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:134911532 G>C maps to NM_004441.4 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr5:139744178 C>T maps to ENST00000507527 Y564Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr1:24083515 G>T maps to NM_003198.2 E746*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr1:245849236 C>A maps to NM_018012.3 S984S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr21:47421897 G>A maps to NM_001848.2 A660A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr11:1904666 C>T maps to ENST00000381758 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr12:3390976 C>T maps to ENST00000407263 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr19:41062019 G>A maps to NM_020971.2 V1705V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:38135138 T>C maps to NM_007335.2 G600G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr3:13542246 C>T maps to NM_024827.3 G149G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr14:64580249 C>T maps to NM_182914.2 D4267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr2:179585678 G>A maps to NM_133378.4 D6445D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr17:79873381 G>A maps to NM_016538.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr16:70508757 C>T maps to NM_145059.2 R741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr7:73604628 C>T maps to NM_022170.1 F154F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr19:39334539 A>G maps to ENST00000221419 N274N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr5:112876725 T>C maps to NM_022828.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr4:9783991 C>T maps to NM_000798.4 C113C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr11:44626915 C>T maps to NM_002231.3 F91F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr19:52130799 G>A maps to ENST00000222107 H399H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr1:120539833 A>T maps to NM_024408.2 C179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5767-01A-11D-1786-08 chr6:38548003 G>A maps to NM_052893.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chrX:128599697 G>T maps to NM_003069.3 Y943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr10:26581401 C>T maps to NM_001134366.1 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr12:133249851 C>T maps to ENST00000455752 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr1:158368836 C>T maps to NM_001004475.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:29295480 G>A maps to NM_001029883.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr19:31769516 C>T maps to NM_020856.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr10:127737878 G>A maps to NM_003474.4 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr14:21796692 C>A maps to NM_020366.3 Y1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr12:6964974 G>A maps to NM_001098536.1 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:170677647 G>A maps to NM_014168.2 F120F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr8:142226016 G>A maps to NM_001080431.1 Y543Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr2:189874961 T>C maps to NM_000090.3 C1294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chrX:117700565 G>T maps to ENST00000276204 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr16:2903246 G>A maps to NM_022119.3 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr5:171299982 C>A maps to NM_012300.2 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr19:17571712 G>A did not map to a codon.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr7:137082143 A>T maps to NM_004717.2 L987*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5768-01A-11D-1576-08 chr17:15976857 A>C maps to ENST00000395857 T1248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:7075114 C>T maps to NM_024341.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:63175049 G>A maps to NM_139318.3 Q715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:89480251 G>A maps to NM_018284.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr12:8804282 G>T maps to NM_003480.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:62393500 C>T maps to NM_176877.2 Q1224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:22415643 C>T maps to NM_005775.4 S139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:108861450 C>T maps to NM_001098268.1 K722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:1616603 C>T maps to ENST00000357934 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr18:77896568 T>C maps to NM_014913.3 F1091F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:94756666 T>C maps to NM_001100607.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:149885320 C>T maps to NM_014849.3 K24K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:228456387 C>T maps to NM_001098623.1 R1673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr9:139401817 G>A maps to NM_017617.3 N1194N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr7:143771566 G>A maps to NM_001004488.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:7723411 G>T did not map to a codon.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:55339543 G>A maps to NM_138962.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:5033902 C>T maps to NM_004505.2 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:231830154 T>C maps to NM_001164537.1 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr15:66618501 C>T maps to NM_001143688.1 H667H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr9:101980872 G>A maps to NM_033087.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr8:22051964 C>T maps to NM_006129.4 C435C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:58121388 C>T maps to NM_022070.4 P1027P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr16:2239047 G>A maps to NM_020764.3 N199N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:42636102 G>A maps to NM_001466.3 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:40811927 C>T maps to NM_016437.2 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:18313412 C>T maps to NM_002866.4 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr17:65026807 G>A maps to NM_014405.3 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:170938347 C>T maps to ENST00000442603 L1917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:91647608 T>C maps to NM_001102368.1 C270C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr19:1068741 C>T maps to NM_012292.2 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr13:111156529 G>T maps to NM_001846.2 G1441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr1:185269160 A>G maps to NM_006469.4 L491L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr14:90650707 C>T maps to NM_022054.2 Y196Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr2:101656774 G>A maps to NM_001102426.1 H300H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr3:46724744 C>A maps to NM_147129.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chrX:153587626 G>A maps to NM_001110556.1 G1430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5769-01A-11D-1576-08 chr20:25195564 C>T maps to NM_001247.2 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr20:57290252 C>T maps to NM_024663.3 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr5:75427790 C>T maps to NM_014979.1 D72D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr8:55540710 T>A maps to NM_006269.1 C1423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr20:1276942 C>A maps to ENST00000381876 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr14:96800091 G>A maps to NM_018036.5 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr16:418563 C>T maps to NM_006428.4 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5771-01A-21D-1576-08 chr12:123834910 A>G maps to NM_001167856.1 I26I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:215890473 G>A maps to NM_173076.2 R404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr2:80530233 C>A maps to NM_178839.4 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140237081 G>A maps to NM_018901.2 A483A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr19:57175471 G>A maps to NM_001005850.1 H387H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr10:105798242 G>A maps to NM_000494.3 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:153391727 C>T maps to NM_176823.3 A83A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-CH-5772-01A-11D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr22:26701984 C>T maps to NM_021115.4 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr7:43484981 C>T maps to NM_015052.3 D737D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chrX:99662412 G>A maps to NM_001184880.1 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:155028576 C>T maps to NM_207197.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr19:45656260 C>A maps to NM_198478.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr4:69693266 G>A did not map to a codon.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:63543827 A>G maps to NM_000706.3 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chrX:24516990 C>T maps to NM_001142386.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr9:130630298 G>A maps to ENST00000223836 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:66469125 G>A maps to NM_006946.2 A915A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr19:22154451 A>G maps to NM_007153.3 L1128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140794394 G>A maps to NM_018913.2 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr12:13717456 G>T maps to NM_000834.3 A905A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:48557075 T>C maps to NM_018346.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr17:8792522 C>T maps to NM_001142633.1 G276G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:133712383 G>A maps to NM_174927.1 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr6:1390757 G>A maps to NM_001452.1 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:25617206 G>A maps to ENST00000357542 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr15:89871739 G>A maps to NM_002693.2 D399D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:128844093 C>A maps to NM_001142685.1 E986*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr5:140720421 G>A maps to NM_018915.2 T628T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr16:83704516 G>C maps to ENST00000268613 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr20:44869812 G>A maps to NM_021248.1 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr11:92088334 C>A maps to ENST00000298047 V1019V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:248551358 C>T maps to NM_001005471.1 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5772-01A-11D-1576-08 chr1:212274087 T>C maps to NM_016448.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:98192173 C>T maps to NM_001270.2 Q1681Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr7:99631795 C>T maps to NM_003439.1 G556G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:128428779 A>C maps to NM_001159542.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:67305046 C>T maps to NM_004594.2 T875T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr1:202245637 C>T maps to NM_001017403.1 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr19:57065113 G>A maps to NM_020828.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr19:15756623 C>A maps to NM_000896.2 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:67234422 G>A maps to NM_024712.3 W214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr10:124376759 T>G maps to ENST00000368915 S1625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr15:93162647 A>G did not map to a codon.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr2:9484929 G>A did not map to a codon.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr2:74072295 A>G maps to NM_213622.1 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr1:46497979 C>T maps to NM_015112.2 I1106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr12:59283854 G>A maps to NM_153377.3 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr16:3778252 C>T maps to NM_004380.2 A2265A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:23290498 C>T maps to NM_004901.3 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:140553129 C>T maps to NM_018940.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr8:72963063 G>A maps to NM_007332.2 G618G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr11:33373267 T>C maps to NM_005734.3 H974H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr3:47963255 G>A maps to ENST00000426837 Y193Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr7:120385959 C>T maps to NM_012281.2 R532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr22:36960763 G>A maps to NM_006078.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr5:162868106 T>A maps to NM_199246.1 C96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5788-01A-11D-1576-08 chr15:55964736 C>T maps to NM_173814.4 Q649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr11:117864124 G>A maps to NM_001558.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr10:56287577 G>T maps to NM_001142763.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr8:23114022 C>T maps to NM_152272.3 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr14:92608696 T>C did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr2:33172886 T>C did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr20:1433674 C>T did not map to a codon.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr1:237801683 C>T maps to NM_001035.2 L2274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr6:33287899 C>T maps to NM_001350.4 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr19:9075832 C>T maps to NM_024690.2 E3871E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr7:92147135 G>A maps to NM_000466.2 N231N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr7:45744118 C>A maps to NM_021116.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5789-01A-11D-1576-08 chr2:88478452 G>A maps to NM_018271.3 Q241Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr19:33584365 C>T maps to NM_018025.2 A132A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr18:8113636 C>A maps to NM_001105244.1 L670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr8:139278044 G>A maps to NM_015912.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr2:27258871 G>A maps to NM_017727.4 Q224Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr10:32337437 T>C maps to NM_004521.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr20:31427558 C>G maps to NM_012325.2 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:51746688 C>T maps to NM_000839.3 G217G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:10251300 G>A maps to NM_001570.3 P151P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr5:137893675 C>A did not map to a codon.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr6:146480671 C>T maps to NM_000838.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr3:48624752 C>T maps to NM_000094.3 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5790-01A-11D-1576-08 chr16:85936701 T>C maps to NM_002163.2 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr8:77764256 C>T maps to NM_024721.4 H1700H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr17:3992019 C>T maps to NM_015113.3 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr10:101455822 C>T maps to NM_020354.3 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr2:228155517 C>A maps to NM_000091.4 G1042G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr10:89690801 G>A did not map to a codon.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:120615276 G>A maps to NM_006836.1 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:48737262 C>A maps to NM_152320.2 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr2:229890758 T>A maps to NM_017933.4 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr8:133196584 G>A maps to NM_004519.2 A169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr1:196971636 G>A maps to ENST00000367414 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr11:124857793 C>T maps to NM_025004.2 Q558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr12:109290786 C>T maps to NM_001917.4 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr1:230338964 C>T maps to NM_004481.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5791-01A-11D-1576-08 chr21:18924179 G>A maps to NM_001338.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:158576872 C>T maps to NM_001004478.1 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr9:94172249 G>C maps to NM_005384.2 S256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr7:100807836 G>A maps to NM_003378.3 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr1:182550488 G>A maps to NM_021133.3 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr2:48915654 A>T maps to NM_000233.3 Y427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr3:49928942 C>T maps to NM_002447.2 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr20:31424468 A>G maps to NM_012325.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr17:34147367 C>T maps to NM_139215.1 Q73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr19:10089566 C>T maps to NM_015719.3 P988P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr8:3889496 G>A maps to NM_033225.5 H180H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5792-01A-11D-1576-08 chr5:79029069 A>G maps to NM_153610.3 K1494K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr9:104192138 G>A maps to NM_000035.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr19:54754888 T>C maps to ENST00000450632 R582R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr3:49755884 G>A maps to NM_198722.2 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr9:133799130 C>A maps to NM_001145106.1 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr12:110765383 T>A maps to NM_170665.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:45262493 C>T maps to NM_021072.2 P734P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr19:7691146 C>A maps to NM_020196.2 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr19:39965234 G>T maps to NM_003169.3 T967T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:101813485 G>A maps to NM_173488.3 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr7:99686976 C>G maps to NM_006833.4 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr2:182376433 T>C maps to NM_000885.4 F618F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr6:1624709 G>A maps to NM_001500.2 F351F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr5:34826504 C>G maps to NM_001145521.1 S907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5794-01A-11D-1576-08 chr1:158585064 G>A maps to NM_003126.2 D2243D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr18:21426326 C>T maps to ENST00000416669 G1264G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr14:38060571 A>C maps to NM_004496.2 *473E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr5:140554609 C>T maps to NM_018940.2 R732*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chrX:102337711 G>A maps to NM_022052.1 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr5:140188928 C>T maps to NM_018907.2 T719T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr8:86249176 G>A maps to NM_001738.3 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr12:111652017 C>T maps to NM_015267.3 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr4:52861921 G>A maps to NM_001024611.1 N422N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr11:55606580 G>A maps to NM_001005496.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr4:41621298 G>A maps to NM_014988.2 E259E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5494-01A-01D-1576-08 chr12:130935763 G>A maps to NM_015347.4 S143S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr2:105706376 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr11:57182086 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:62946845 G>A maps to ENST00000393630 V1035V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:32023934 G>T maps to ENST00000375244 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr4:175897498 G>T maps to NM_014269.4 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:54735286 T>C maps to NM_001010872.1 D81D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:5964827 C>T maps to NM_015102.2 K664K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:96651186 C>T maps to NM_006581.3 N52N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:8212298 G>A maps to NM_032447.3 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr19:3643242 G>A maps to NM_012398.2 Y549Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:60140572 G>A maps to NM_005121.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr10:48389851 C>T maps to NM_002900.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:21103088 C>G did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr1:16918793 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:7673933 G>A maps to NM_020877.2 K1386K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr7:3681626 A>T maps to NM_152744.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr17:34174029 C>G did not map to a codon.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:160864676 G>A maps to ENST00000392145 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr16:27802747 G>C maps to NM_001109763.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr16:20043983 G>T maps to NM_001002911.2 I45I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr8:99440308 G>T maps to NM_020697.2 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr21:27840879 G>T maps to ENST00000435845 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr20:32379197 G>T maps to ENST00000375200 E814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr12:66725337 A>G maps to NM_033647.2 V1025V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr6:155451341 C>T maps to ENST00000456144 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr19:42312920 G>A maps to NM_001815.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:29314299 A>G maps to NM_001166005.1 E117E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr20:31023727 G>A maps to ENST00000375687 A1071A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr17:42293126 G>A maps to NM_014233.2 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:170913386 C>T maps to NM_021647.6 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr6:119510997 G>A maps to NM_005907.2 I459I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:119576826 G>A maps to NM_015836.3 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:130766662 G>A maps to ENST00000514667 Q1502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr16:81944187 C>T maps to NM_002661.2 Y599Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr1:27106760 A>G maps to NM_006015.4 K2124K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr17:66267451 T>C maps to NM_004694.4 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:70721016 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:149247705 G>A maps to NM_000440.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr4:123192754 G>A maps to NM_015312.3 V2692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr3:31710252 C>T maps to NM_017784.4 W659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr15:78403581 G>A maps to NM_006383.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5496-01A-01D-1576-08 chr5:74091852 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr20:31021260 C>T maps to ENST00000375687 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr11:134054636 C>T maps to NM_015261.2 K782K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr8:145534872 C>T maps to NM_005526.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr19:14829746 C>T maps to NM_032433.2 C536C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr5:140176552 G>A maps to NM_018905.2 S668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr2:211454903 G>A maps to NM_001122633.1 A268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr5:139201585 G>A maps to NM_032289.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr19:35232874 C>G maps to ENST00000392232 S574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr20:34458922 A>G maps to NM_016436.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5497-01A-02D-1576-08 chr1:24998070 G>A maps to NM_005839.3 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr21:41684281 C>T maps to NM_001389.3 P596P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr9:139847393 G>A maps to NM_178536.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr19:44352237 C>G maps to NM_181845.1 T495T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr15:33954938 C>T maps to NM_001036.3 G1736G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr12:55820711 C>T maps to NM_001005183.1 I225I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:48059589 C>T maps to NM_001190274.1 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr20:35668589 C>T maps to NM_002895.2 K623K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr3:49723303 C>T maps to NM_020998.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr1:197104364 G>C maps to NM_018136.4 P678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr2:143790836 C>T maps to NM_003937.2 R330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr10:106974253 C>T maps to NM_014978.1 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr7:121943287 G>A maps to NM_001024613.2 C293C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr12:97085089 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr3:108112994 G>A maps to NM_014981.1 S1734S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr7:48327659 G>A maps to NM_152701.3 A2980A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr5:140573540 C>T maps to NM_018930.3 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr6:131490306 A>G maps to ENST00000431975 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr6:117645560 C>A maps to NM_002944.2 E1859*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr15:65917479 A>G maps to NM_004727.2 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr1:152732099 G>A maps to NM_001025231.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr14:65239588 G>T maps to ENST00000389723 I1758I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr4:155254245 G>A maps to NM_017639.3 N539N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:22001954 T>G maps to NM_003423.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:11453675 C>A maps to NM_198536.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:42301581 G>A maps to NM_001815.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr19:55106787 G>A maps to NM_006863.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5499-01A-01D-1576-08 chr2:166165900 G>A maps to NM_001040142.1 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:25467185 C>T maps to NM_175629.1 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr12:56552379 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr8:10285773 C>T maps to NM_012331.3 C220C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr20:47692014 C>T maps to NM_001316.2 I431I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:121746684 C>T maps to NM_005270.4 D1065D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr11:133790979 G>A maps to NM_014987.1 A880A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr10:12200104 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr5:2749499 G>A maps to NM_033267.4 D217D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr5:205600 G>A maps to NM_145265.2 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5501-01A-01D-1576-08 chr2:132237010 G>C maps to NM_080386.2 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr2:141259354 G>A maps to NM_018557.2 G2917G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr5:140605444 C>T maps to NM_018934.2 R790*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr17:7240073 C>T maps to NM_014716.3 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chrX:70357095 C>A maps to ENST00000333646 R1871R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5502-01A-01D-1576-08 chr8:28385110 A>T maps to NM_017412.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr17:58009015 G>A maps to NM_003161.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr17:33769198 G>A maps to NM_144682.5 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr11:2182080 G>A maps to NM_001042376.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr6:43400461 C>T maps to NM_033450.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr3:112546283 G>A maps to NM_001008784.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5503-01A-01D-1576-08 chr9:428368 C>A maps to NM_203447.3 S1449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr12:131498746 C>T maps to NM_198827.3 I445I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr3:108347995 A>G maps to NM_014648.3 E223E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr7:121652282 G>A maps to NM_002851.2 E1061E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chrX:14748514 C>T maps to NM_002063.3 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr10:64159481 C>T maps to NM_014951.2 G386G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr2:219353101 G>T maps to NM_020935.2 L505L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr5:173067 C>T maps to NM_052909.3 C1013C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr10:127525311 C>A maps to NM_018180.2 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr11:119002675 C>G maps to NM_198971.1 R220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr1:163122354 C>T maps to NM_003617.3 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr6:132203594 C>T maps to NM_006208.2 Y737Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr4:1980395 C>T maps to NM_133335.3 D1286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr1:55521762 C>T maps to NM_174936.3 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr12:56030938 G>A maps to NM_206899.1 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr9:129642272 C>T maps to ENST00000319119 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5504-01A-01D-1576-08 chr2:175618297 G>A maps to NM_001039523.2 N262N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr4:155256173 C>G maps to NM_017639.3 G354G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr6:31797487 C>G maps to NM_005346.4 A587A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chrX:153224169 A>C maps to ENST00000369984 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr11:122848488 G>A maps to NM_001098169.1 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr1:155451979 A>T maps to ENST00000368346 C227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr2:209358095 G>T maps to NM_005048.2 V455V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr15:59064094 T>G maps to NM_001040450.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr16:72130067 C>T maps to NM_014003.3 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr8:8749968 C>A maps to NM_004225.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr17:40476776 G>A maps to NM_139276.2 R518*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr2:242794938 G>T maps to NM_005018.2 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr9:35042437 C>T maps to NM_203299.2 R63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr11:43513625 C>T maps to NM_018259.5 D1069D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr17:76471407 G>A maps to ENST00000389840 D2807D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5506-01A-01D-1576-08 chr12:104487294 T>G maps to NM_013320.2 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr1:149884959 G>A maps to NM_014849.3 R145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr6:51524057 G>A maps to NM_138694.3 C3622C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr13:45594564 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr9:77448964 T>C maps to NM_017662.4 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr20:39990960 G>A maps to NM_052846.1 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:47036898 A>G maps to NM_015175.1 A558A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr7:106509964 C>T maps to NM_002649.2 D653D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr22:26688422 C>A maps to NM_021115.4 S49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr22:31059966 G>A maps to NM_152511.3 F8F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr6:111726772 C>T maps to NM_002912.3 A155A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr9:138586194 C>T maps to NM_001012415.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5507-01A-01D-1576-08 chr3:51347718 C>T maps to NM_004947.4 F993F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr5:148206405 C>T maps to NM_000024.5 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr6:87969898 A>G maps to NM_015021.1 Q2184Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr11:71850177 G>T maps to ENST00000442948 G113G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr19:2041131 G>A maps to NM_199054.2 C339C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr1:186915808 A>G maps to NM_024420.2 K358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr21:30255332 A>G maps to NM_013240.3 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr7:87104730 C>T maps to NM_018849.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr18:19154389 T>A maps to NM_052911.2 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr19:53855283 G>A maps to NM_138374.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr6:41029414 G>A maps to NM_006789.3 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5508-01A-02D-1576-08 chr14:36039875 T>G maps to NM_194301.2 T1975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr8:37623075 G>A maps to NM_007198.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr11:119045199 C>T maps to NM_024618.2 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr20:57769547 G>A maps to NM_178457.1 T1158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr1:156263001 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr12:88568464 T>C maps to NM_181783.3 D427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr2:189875580 A>T maps to NM_000090.3 K1407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr3:33400491 C>T maps to NM_012157.3 C33C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr4:74005374 T>G maps to NM_032217.3 G986G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr7:100693834 T>C maps to NM_001040105.1 L4265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr6:27861557 G>A maps to NM_003527.4 E106E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5509-01A-01D-1576-08 chr4:153881742 C>T maps to NM_033393.2 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr11:43345104 A>C maps to NM_001142930.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr3:64554180 G>A maps to NM_182920.1 Q1463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:43777765 A>G maps to ENST00000389420 C1489C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr8:30958413 G>A maps to NM_000553.4 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr3:63898513 G>A maps to NM_001177387.1 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:120150459 G>T maps to ENST00000392521 P1540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chrX:37027784 C>T maps to NM_001013736.2 R434R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr1:198233328 A>G maps to NM_133494.2 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr13:109779875 G>A maps to NM_015011.1 A1321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5510-01A-01D-1576-08 chr12:120635151 C>T maps to NM_053275.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:41611324 G>A maps to NM_001079675.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr9:112185101 C>T maps to NM_002829.3 V344V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr15:85326136 G>A maps to NM_014630.2 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636498 C>T maps to NM_001466.3 F481F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr18:6943332 C>A maps to NM_005559.2 V2971V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr6:152832184 T>A maps to NM_182961.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636060 C>G maps to NM_001466.3 Y335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr8:113585823 G>A maps to NM_198123.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:30986137 G>A maps to NM_015194.1 F780F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr5:156184678 C>T maps to NM_000337.5 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42636210 C>T maps to NM_001466.3 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr1:145015937 C>T maps to NM_001198832.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr9:134497350 C>T maps to NM_198679.1 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr17:42635478 C>T maps to NM_001466.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr6:36767796 G>T maps to NM_020939.1 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr11:133790583 G>T maps to NM_014987.1 I1012I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr12:14628822 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr1:158669836 G>T maps to NM_001005279.1 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr6:106764040 G>A maps to NM_004849.2 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr10:93600427 A>G maps to NM_025235.3 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr17:62007650 G>A maps to NM_001039933.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr3:149040065 C>A maps to NM_138786.3 G190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr15:45965848 G>T maps to NM_021199.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr7:141315345 G>T maps to NM_018238.3 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr16:87678350 C>T maps to NM_020655.2 G290G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5512-01A-01D-1576-08 chr1:156568874 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr14:21871247 A>G maps to NM_001170629.1 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr1:113636958 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr7:95750980 A>G maps to NM_001160210.1 I610I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:213886795 C>G maps to ENST00000342002 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:29148006 T>G maps to NM_015131.1 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chrX:2407935 G>A maps to NM_004729.3 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr1:55280636 C>T maps to NM_001110533.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chrX:144337273 G>T maps to NM_001009614.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chrX:107159357 A>G maps to NM_012216.3 T400T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr17:7495580 T>C maps to NM_004860.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr16:25251247 G>T maps to NM_001012981.4 T931T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr5:82808054 C>T maps to NM_004385.4 C294C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr5:79026180 C>T maps to NM_153610.3 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr2:15468433 C>T maps to NM_015909.2 G1450G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr19:5598869 G>A maps to NM_014649.2 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr4:9828094 T>G maps to NM_020041.2 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr10:118357364 C>T maps to NM_006229.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr17:73887231 C>T maps to NM_173547.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr16:24373177 C>T maps to NM_006539.3 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5514-01A-01D-1576-08 chr15:42602621 G>A maps to NM_198141.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr19:12940771 G>A maps to NM_031429.1 R40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr11:66082755 C>T maps to NM_020404.2 Q581Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr16:52484401 C>T maps to ENST00000407228 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5515-01A-01D-1576-08 chr17:33690214 G>T maps to NM_152270.3 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr15:43827081 G>A maps to NM_001130858.2 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:39982550 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:160688256 C>T maps to NM_001198759.1 E1294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:18579844 G>C maps to NM_001040697.1 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr2:160710868 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr20:61471945 C>T maps to NM_001853.3 G639G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr3:113152409 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:49186292 C>T maps to NM_004476.1 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr1:12336132 C>T maps to NM_015378.2 R830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr1:91843737 T>A maps to NM_001017975.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr7:138437473 G>A maps to NM_130840.2 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr12:51089054 A>T maps to NM_173602.2 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr22:51008808 G>A maps to NM_152245.2 S685S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr4:9828062 G>A maps to NM_020041.2 I527I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr3:57108292 T>A maps to NM_181727.1 *191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr11:13424826 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr13:25376710 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr4:158257611 C>T maps to NM_000826.3 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr19:5456786 C>T maps to NM_181710.3 Q429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5516-01A-01D-1576-08 chr4:70798272 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr16:67865091 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr12:113733847 A>T maps to NM_001143819.1 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr16:55601018 C>T maps to NM_032330.1 D117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr19:52937266 G>A maps to NM_001143939.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr4:155242137 C>T maps to NM_017639.3 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr6:39828786 G>A maps to ENST00000398904 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr22:45128195 G>C maps to ENST00000352766 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chrX:41000650 G>A maps to NM_001039590.2 E376E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr5:137277735 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr7:154667654 C>T maps to NM_130797.2 F641F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5517-01A-01D-1576-08 chr5:140558061 T>A maps to NM_019120.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:28117447 C>T maps to NM_004899.3 R9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr15:51750825 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr1:70502286 T>C maps to NM_020794.2 H718H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr6:46623670 C>A maps to NM_004277.3 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:36778887 G>A maps to NM_033403.1 Y421Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr7:48315046 C>T maps to NM_152701.3 V1928V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr16:83065741 C>T maps to ENST00000268613 F95F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:121413150 T>C maps to ENST00000393667 E2073E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr1:15546031 C>T maps to NM_018022.2 N185N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr10:103789493 G>A maps to NM_024541.2 C105C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr17:75205503 C>G maps to NM_001039573.2 L519L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr11:113704217 G>C maps to NM_020886.2 S228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:25469137 C>T maps to NM_175629.1 W440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chrX:13337264 C>T maps to NM_001135995.1 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr10:70940277 C>T maps to NM_003171.3 D77D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr16:23999907 C>T maps to NM_002738.6 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr12:78515854 G>T maps to NM_014903.4 T1295T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EJ-5518-01A-01D-1576-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr3:187451334 G>A maps to ENST00000449623 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr1:158325959 G>A maps to ENST00000434258 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5518-01A-01D-1576-08 chr2:241831175 C>T maps to NM_001085437.1 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr18:12706676 G>T maps to NM_020232.4 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:14910837 G>C maps to NM_198944.1 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:17169088 C>T maps to NM_004686.4 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:7827735 G>T maps to NM_004732.2 I236I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:33745724 C>T maps to NM_170672.2 H114H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:42284562 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr7:48318293 T>C maps to NM_152701.3 T2501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr3:45942585 C>T maps to NM_031200.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:25745378 C>A maps to NM_022659.2 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:34100898 C>T maps to NM_000841.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr13:50123714 G>A maps to NM_018191.3 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:17412830 C>T maps to NM_148172.1 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:152275292 A>G maps to NM_002016.1 D4023D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:85510884 G>A maps to NM_018298.9 F53F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:95158180 G>A maps to NM_001144663.1 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:44040308 A>T maps to NM_022436.2 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:46757762 C>G maps to NM_018976.4 L299L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:95676989 C>G maps to NM_017697.3 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:2878236 C>T maps to NM_024967.1 C427C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr22:30736750 T>C maps to NM_005877.4 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:97098575 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr11:119228894 G>A maps to NM_004205.4 F435F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr5:129520760 A>G maps to NM_175856.4 E642E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr6:110752469 C>T maps to NM_033125.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr1:186055462 T>G maps to NM_031935.2 G2990G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr2:215645850 G>A maps to NM_000465.2 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:56598641 G>A maps to NM_004574.3 R363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr17:5264855 A>G maps to NM_004703.4 Q483Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr4:76813114 G>A maps to NM_006239.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr8:131249204 C>G maps to NM_018482.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr19:14938094 C>A maps to NM_017506.1 *320L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr12:69094532 C>A maps to NM_020401.2 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr21:45959619 C>T maps to NM_198691.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5519-01A-01D-1576-08 chr20:16360551 C>A maps to NM_024704.4 E699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr20:17622554 T>A maps to ENST00000377813 K691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:72370578 G>T maps to NM_138782.2 R530R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:180582178 G>A maps to NM_206880.1 V79V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr11:4791051 A>T maps to ENST00000380383 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:247614411 G>T maps to NM_001004492.1 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr12:7061280 C>T maps to ENST00000416215 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr3:151545614 C>T maps to NM_001086.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr9:71628978 G>A maps to NM_002732.3 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr13:102047575 C>T maps to NM_052867.2 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:10394817 G>A maps to NM_000201.2 Q249Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:25505421 G>A maps to NM_175629.1 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:158064570 C>T maps to ENST00000368173 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:159790452 C>T maps to ENST00000379346 R912*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:126371607 T>A maps to NM_024582.4 L3146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:5784047 T>C maps to NM_001134316.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr7:77567151 C>T maps to ENST00000427986 N488N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr1:111147493 C>T did not map to a codon.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr4:126371767 T>C maps to NM_024582.4 Y3199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr3:148760004 A>T maps to NM_003071.3 I715I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:101607289 C>T maps to NM_002518.3 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr2:15378657 C>T maps to NM_015909.2 E1959E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr15:65790301 G>A maps to NM_197960.2 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr5:156899409 C>T maps to NM_001099287.1 Y281Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr19:10625417 G>A maps to NM_001166215.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr9:130653031 G>A maps to NM_013443.3 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5521-01A-01D-1576-08 chr12:55420975 C>A maps to NM_021191.2 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:74646120 G>A maps to NM_000859.2 Q234Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:1497833 G>A maps to ENST00000357934 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:140735372 C>T maps to NM_018917.2 R202R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr12:101764853 C>T maps to NM_014503.2 L2236L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr2:242138765 C>T maps to NM_001001891.3 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr4:48851970 T>C maps to NM_001168254.1 C88C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr19:13211895 T>G maps to NM_005583.4 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr10:85904773 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr11:64109489 C>A maps to NM_032251.5 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr17:56345180 C>T maps to NM_006151.2 N655N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr3:44672663 G>A maps to NM_006991.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:180338567 G>A maps to NM_001040462.2 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:2910128 T>A maps to NM_033225.5 S2505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr5:140725402 C>T maps to NM_018916.3 N601N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr1:1333665 G>A maps to NM_030937.4 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5522-01A-01D-1576-08 chr8:41572580 G>A maps to ENST00000415018 T538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr1:86916414 C>T maps to NM_006536.5 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr12:25148934 C>T maps to NM_001101339.1 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr12:124395092 G>A maps to NM_207437.3 K3218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr17:42085836 C>T maps to NM_153006.2 G491G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr2:211421555 A>G maps to NM_001122633.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr18:54591237 G>A maps to NM_015285.2 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr2:160706544 C>T maps to NM_001198759.1 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr1:3807510 G>A maps to NM_207356.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr10:129900971 G>C maps to NM_002417.4 P3044P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5524-01A-01D-1576-08 chr17:73627744 G>A maps to NM_004259.5 C411C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr13:26788079 G>A maps to NM_005977.3 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr21:45503101 T>C maps to NM_003274.4 A719A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:120342380 C>T maps to NM_032044.3 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr9:132400167 C>T maps to NM_017873.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr4:141074097 G>T maps to ENST00000509479 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:68947727 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr17:30349139 A>C maps to ENST00000327564 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr10:134942934 T>C maps to ENST00000368577 L1075L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:44099376 G>A maps to NM_001007561.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr12:94763728 T>C maps to NM_001042399.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr12:130839527 C>T maps to NM_004764.4 R423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr6:132195476 A>G maps to NM_006208.2 Q545Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr11:18362865 A>G maps to NM_005316.3 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr15:31294405 G>A maps to NM_002420.4 I1477I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:58101496 C>T maps to NM_001010879.2 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr1:92185485 C>T maps to NM_003243.4 E459E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr19:1058147 C>T maps to NM_019112.3 L1677L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr10:99623790 C>T maps to NM_001010917.1 C81C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr17:38905555 G>C maps to NM_181534.3 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5525-01A-01D-1576-08 chr6:106969053 T>A maps to NM_001624.2 L916*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:88061087 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr19:18898324 C>G maps to NM_000095.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr2:76975913 G>A maps to NM_001134745.1 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr15:65041629 G>A maps to NM_194272.1 N89N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr20:42788454 G>A maps to NM_020433.4 H324H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:88967910 C>A did not map to a codon.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr16:83999179 C>T maps to NM_013370.3 Y417Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chr1:214171236 C>T maps to NM_002763.3 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5526-01A-01D-1576-08 chrX:34961793 T>C maps to NM_152631.2 H282H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr14:71215543 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr22:42610894 A>G maps to NM_005650.1 F139F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:157558992 C>G did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:14687627 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr4:36130283 T>G maps to NM_015230.2 R1171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr7:86468359 C>T maps to NM_000840.2 S510S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:186331025 C>T maps to ENST00000273784 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:114510460 T>C maps to ENST00000426820 L890L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr19:36431058 G>A maps to NM_024509.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:148207350 T>G maps to NM_000024.5 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr16:89789104 T>A maps to NM_001113525.1 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:37125218 A>G maps to NM_006309.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr4:55956220 G>A maps to NM_002253.2 R1032*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr22:32229972 G>A did not map to a codon.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:48865160 T>C maps to NM_019073.2 K214K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr2:168099281 T>G maps to NM_152381.5 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr12:4874639 G>A maps to NM_017417.1 A563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr12:63976242 T>C maps to NM_173812.4 L556L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr2:225670000 G>A maps to NM_014689.2 R1325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr17:19559758 G>A maps to NM_001031806.1 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr1:209953927 C>T maps to NM_025228.2 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr5:171821587 T>G maps to NM_001017995.2 I96I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:108724126 G>A maps to NM_014429.3 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chrX:39914705 A>G maps to NM_001123385.1 Y1552Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr3:25833003 T>C maps to NM_017897.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5527-01A-01D-1576-08 chr14:51446110 G>A maps to ENST00000338969 N769N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr8:28633368 G>A maps to NM_018250.3 I490I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr2:125521375 C>T maps to NM_130773.2 R787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr2:204039931 C>G maps to NM_001114132.1 S2100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr8:117878923 G>A maps to NM_006265.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:111216033 G>A maps to NM_002232.3 I466I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr19:1418347 G>A maps to NM_018959.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:140250898 G>A maps to NM_018902.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:55472068 C>T maps to NM_024669.2 A74A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr20:18505661 C>T maps to NM_001172745.1 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr5:53752033 T>C maps to NM_006308.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr19:15132480 G>A maps to NM_173482.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr15:85410591 C>T maps to NM_020778.4 R1792*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:9171451 G>A maps to NM_024980.4 D160D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chrX:83411184 A>T maps to NM_014496.4 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr11:47345220 G>C did not map to a codon.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr16:71419499 C>T maps to NM_001740.4 D216D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr6:32021195 G>A maps to ENST00000375244 R2920R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr17:73663473 C>T maps to NM_013260.6 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5530-01A-01D-1576-08 chr1:181727099 C>T maps to ENST00000357570 F1449F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr1:86590962 G>T maps to NM_152890.5 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chrX:48386619 A>T did not map to a codon.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:146824229 G>A maps to ENST00000508784 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr18:14104993 A>C maps to NM_145287.3 P515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr12:53567191 G>A maps to NM_015989.4 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr17:39190953 G>A maps to NM_030966.1 C40C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr16:9858033 C>A maps to NM_000833.3 E1123*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr6:44221298 C>T maps to NM_007355.2 G713G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr11:1081736 C>T maps to ENST00000441003 N555N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:140811116 C>T maps to ENST00000509479 Q491Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr1:212118152 C>T maps to NM_015434.3 L858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5531-01A-01D-1576-08 chr6:55142194 T>C maps to NM_001526.3 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr15:51855613 C>T maps to NM_001174116.1 W177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr12:112516058 A>G maps to NM_024953.3 Y199Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr6:28227526 G>A maps to NM_001007531.1 E126E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr10:123954656 C>T maps to NM_206862.2 P1979P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr5:149360520 T>A maps to NM_000112.3 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr1:240371600 C>T maps to ENST00000406993 P1306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr19:55148262 T>G maps to ENST00000427581 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr11:76868350 G>A maps to NM_000260.3 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr16:12136838 C>T maps to NM_032167.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr12:6172164 C>T maps to NM_000552.3 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr13:29600583 G>A maps to NM_001033602.2 T593T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5532-01A-01D-1576-08 chr17:20910261 G>A maps to ENST00000455117 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr11:117066582 C>T maps to NM_001040455.1 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr4:155532985 T>C maps to ENST00000407946 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:38062139 C>T maps to NM_001165958.1 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr10:50666943 G>A maps to NM_000124.2 R1467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:38810913 T>C did not map to a codon.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr1:237754088 T>A maps to NM_001035.2 A1319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr12:57112064 T>C maps to NM_001113203.1 P1083P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr17:2076131 C>T maps to NM_017575.4 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr5:140183010 C>T maps to NM_018906.2 S743S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr11:74053511 C>T maps to NM_173582.3 K542K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:42569513 C>T maps to NM_002088.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr5:136963995 C>T maps to NM_017415.2 R527R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:46299170 C>A maps to NM_030785.3 E704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr1:240370946 G>A maps to ENST00000406993 P1088P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr19:6216423 C>T maps to NM_005934.3 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr19:44103388 G>A maps to NM_024327.2 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:157105281 T>A maps to NM_001145312.1 K89*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr19:44515530 C>A maps to NM_006300.3 S447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chrX:153039435 C>T maps to NM_005393.2 A1134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:190862185 A>T maps to NM_004477.2 K8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr12:15710428 G>T maps to NM_030667.1 E867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr5:148747556 G>A maps to NM_024028.3 E275E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:62599225 C>T maps to ENST00000506720 H451H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:138451633 C>A maps to NM_019035.3 E537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr4:166234519 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr6:101098515 T>C maps to NM_006828.2 V1050V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr5:110097208 C>T maps to NM_138773.1 D328D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:92709885 G>A maps to NM_001012425.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:3328641 C>T maps to NM_022114.3 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr13:32761790 C>T maps to NM_023037.2 R1197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr11:44289105 G>A maps to NM_021926.3 R282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7115-01A-11D-2114-08 chr1:107600026 C>T maps to NM_018137.2 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr7:102087366 C>T maps to NM_032831.2 F211F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr5:140795087 G>A maps to NM_018913.2 T782T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr17:76168028 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr11:109294694 C>T maps to NM_207645.3 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr12:112237729 G>A maps to NM_000690.2 Q423Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr12:55945168 C>G maps to NM_001005494.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr6:3850539 C>G maps to NM_012135.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr1:157648601 G>A maps to NM_052939.3 D701D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr20:62737950 C>T maps to NM_005286.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr3:148896262 A>G maps to NM_000096.3 S939S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7123-01A-11D-1961-08 chr11:1266203 G>A maps to ENST00000447027 T2701T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr3:133342925 T>C maps to NM_007027.3 V966V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr1:162313728 A>G maps to NM_014697.2 G186G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr17:26910635 G>A maps to NM_006461.3 Q860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr11:1255480 G>A maps to ENST00000447027 A811A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr22:19198012 T>C maps to NM_007098.3 L1024L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr13:28610091 C>T maps to NM_004119.2 K466K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr22:25331313 C>A maps to ENST00000423535 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7125-01A-11D-1961-08 chr15:80866542 A>T maps to NM_014862.3 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr19:49129074 C>A maps to ENST00000443164 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr19:5455561 G>A maps to NM_181710.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr11:60164140 T>C maps to NM_032597.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chrX:153135592 G>A maps to NM_000425.3 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr8:100866332 C>T maps to NM_017890.3 V3597V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr3:58156416 C>T maps to NM_001164317.1 G2610G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr4:76573855 G>A maps to NM_203505.2 R299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr1:148004649 T>C maps to ENST00000310701 E893E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr1:86488274 C>A did not map to a codon.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr4:128726277 C>T maps to ENST00000438626 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr10:64967186 T>G maps to NM_032776.1 S1414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr3:53531239 G>C maps to NM_001128840.1 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr3:10417119 C>T maps to NM_001001331.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr6:170627924 C>T maps to NM_032448.1 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7314-01A-31D-2114-08 chr11:111780949 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr2:212288966 G>A maps to NM_005235.2 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr12:8242591 A>G maps to NM_015509.3 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chrX:153881612 G>A maps to NM_020994.3 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr2:30961159 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr3:142840956 C>G maps to NM_004267.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr17:38073350 C>T maps to NM_001165958.1 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr15:80472566 G>A maps to NM_000137.1 P354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr11:119027720 T>C maps to NM_001142505.1 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr12:57397204 C>T maps to NM_014830.2 T499T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr3:126748889 C>A maps to NM_032242.3 R1682R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr17:17250218 G>A maps to ENST00000379552 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr16:27506670 C>T maps to NM_001520.3 T831T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7315-01A-31D-2114-08 chr8:66619311 T>C maps to NM_014637.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr16:67876807 G>A maps to NM_020457.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:68470882 T>C maps to NM_031966.2 F295F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:140572700 A>G maps to NM_018930.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr2:29295351 C>T maps to NM_001029883.1 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr16:4042211 C>T maps to NM_001116.3 P714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr10:55587259 G>C maps to NM_001142763.1 P1425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr4:48551611 C>T maps to NM_015030.1 W1554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:137520548 G>A maps to NM_005733.2 Q579Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr20:43355878 G>A maps to NM_003881.2 Q228Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr8:17447025 G>A maps to NM_006207.2 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr8:70978695 T>C maps to NM_024504.2 G319G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr20:52198351 C>T maps to NM_006526.2 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr11:44100334 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr9:32543931 A>C maps to NM_005802.4 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr5:13735946 T>C maps to NM_001369.2 L3850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr4:104041394 C>T maps to NM_001813.2 V2413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7317-01A-31D-2114-08 chr1:44442866 G>C maps to NM_004047.3 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr2:96795626 C>T maps to NM_001002036.3 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:899383 G>T maps to NM_001142676.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr1:110607210 G>A maps to NM_006492.2 Q198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:67375931 C>T maps to NM_007103.3 Y46Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr6:64404529 G>A maps to NM_015153.2 Q852Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:118039352 G>A maps to NM_004588.4 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr9:116968049 A>G maps to NM_032888.2 G727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chrX:101972034 T>G maps to NM_138437.5 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:130343427 C>T maps to NM_139055.2 C855C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:71153384 C>A maps to NM_001360.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr17:1563821 G>A maps to NM_006445.3 H1563H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr19:46215457 G>A maps to NM_001080469.1 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr4:155253864 G>A maps to NM_017639.3 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr1:154841765 C>T maps to NM_002249.4 E225E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr11:60640727 C>T maps to NM_207341.2 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr8:38880739 G>A maps to NM_003816.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr4:169227601 T>C maps to NM_017631.5 Q178Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr3:44943339 C>T maps to NM_003241.3 H296H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr8:38880723 G>A maps to NM_003816.2 W265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr5:33630977 C>T maps to NM_030955.2 Q643Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7321-01A-31D-2260-08 chr5:139060932 C>A maps to NM_016463.7 C275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr9:34997171 C>T maps to NM_001135005.1 L393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr22:30163413 A>G maps to ENST00000406782 K9K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr3:194118888 C>T maps to NM_004488.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr16:11363129 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr17:62022974 G>A maps to NM_000334.4 G1155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chrX:10058809 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr1:159035789 A>T maps to NM_004833.1 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr10:133949432 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7327-01A-11D-2114-08 chr11:7982636 C>T maps to NM_176821.3 S174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr12:2022194 C>T maps to NM_172364.4 A140A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr13:48941652 C>T maps to NM_000321.2 Y321Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr10:43882501 G>A maps to NM_001098204.1 G277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr8:75233374 C>A maps to NM_020647.2 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr14:89878583 C>T maps to NM_001085471.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr18:13885199 G>A maps to NM_000529.2 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr10:103990273 T>C maps to NM_005029.3 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr5:150911163 G>A maps to NM_001447.2 R3265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr11:47712124 C>T maps to ENST00000357610 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr7:91691588 C>T maps to NM_005751.4 G1922G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr19:9082694 T>A maps to NM_024690.2 T3040T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr1:144916718 G>A maps to NM_014644.4 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr10:91177945 C>T maps to NM_012420.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr11:55761663 G>A maps to NM_003697.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7328-01A-31D-2114-08 chr10:87407078 G>A maps to NM_017551.2 F691F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr10:27702747 C>T maps to NM_001034842.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr14:92139266 G>A maps to NM_024764.2 L358L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr7:50607642 G>A maps to NM_000790.3 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr1:169953738 T>C maps to NM_014970.2 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr12:67700300 T>C maps to NM_018448.3 V951V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr7:40085625 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr3:72428399 A>T did not map to a codon.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr3:156192554 G>T maps to NM_172159.3 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr5:141242916 C>T maps to NM_032420.2 V993V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr6:49665571 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr15:43815431 A>G maps to ENST00000382031 E825E. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EJ-7330-01A-11D-2114-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr10:15145357 G>A maps to NM_183005.3 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr1:8923005 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr2:120932464 A>G maps to NM_020909.3 L728L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr2:196673405 C>T maps to NM_018897.2 L3361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr20:861825 C>T maps to NM_015985.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr3:51864454 A>T maps to NM_001085479.1 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr15:89424630 G>A maps to NM_178232.2 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7330-01A-11D-2114-08 chr20:2380265 C>T maps to NM_198994.2 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr11:6789257 G>A maps to NM_001004490.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr7:95705499 T>C maps to NM_004411.4 N564N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr17:74396559 G>A maps to NM_022066.3 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr2:26950775 C>T maps to NM_002246.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr10:123843718 A>T maps to NM_206862.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr7:18687445 G>A maps to NM_178425.2 T358T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr19:6750304 G>A maps to ENST00000313244 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr12:12397550 G>T maps to NM_002336.2 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chrX:44969494 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr2:167089855 T>A maps to ENST00000303354 G1307G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr8:39525629 C>T maps to NM_014237.2 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr15:91040569 C>T maps to NM_003870.3 Q1620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr14:65246523 C>T maps to ENST00000389723 L1468L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr17:63553973 C>G maps to NM_004655.3 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr14:63671715 C>T maps to NM_020663.3 N43N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr8:37602101 G>A maps to NM_007175.6 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr20:3214873 G>A maps to NM_001174090.1 N169N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr5:140202763 G>A maps to NM_018908.2 P468P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr3:127642851 C>T maps to NM_207335.2 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr2:137814398 T>G maps to ENST00000272643 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:5289794 A>T maps to NM_005330.3 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:58919680 A>G maps to NM_198847.2 E180E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:4411306 G>A maps to NM_003141.3 C111C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr12:104107520 C>T maps to NM_017564.9 Y1504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:48161137 G>A maps to NM_002843.3 E751E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:26743039 G>T maps to NM_178498.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7781-01A-11D-2114-08 chr11:134181018 G>A maps to NM_001080407.2 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:26365434 C>T maps to NM_007257.5 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:40102430 G>A maps to NM_003718.4 P869P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:165809220 A>G maps to ENST00000409662 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:5239962 C>T maps to NM_139056.2 F816F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:27372110 C>T maps to NM_000418.2 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:37697697 G>A maps to NM_032777.9 A857A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:244724124 G>A maps to NM_001130957.1 E395E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:103867966 G>A maps to NM_001113407.1 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:129931000 C>T maps to NM_014636.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:12460320 C>T maps to NM_015378.2 T3906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:54930847 C>T maps to NM_018398.2 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:23826530 T>A maps to NM_031414.3 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:99150563 C>T maps to NM_153695.3 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:64629881 G>T maps to NM_197941.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chrX:142716668 G>A maps to NM_001184749.1 S752S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:48626075 C>T maps to NM_000094.3 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:14961815 G>A maps to NM_001033855.1 C359C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:163317626 C>T maps to NM_145697.2 F341F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:154179946 T>A maps to NM_001098616.1 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr6:44268379 C>T maps to NM_020745.2 A954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:37524300 C>T maps to ENST00000406505 G502G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:91726085 C>T maps to NM_005751.4 N3271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:136199100 C>T maps to NM_006753.4 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chrX:154490315 G>A maps to NM_171998.2 A138A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:33608947 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:124106407 C>T maps to NM_001414.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr20:1445044 G>A maps to ENST00000476071 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:145722825 C>T maps to NM_032902.5 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:107592540 C>T maps to NM_002291.2 A1069A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:43285946 G>A maps to NM_014753.3 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:160314572 C>A maps to NM_015331.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:140256667 G>A maps to NM_018903.2 A537A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:50302914 G>T maps to NM_014203.2 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr20:56099036 G>A maps to ENST00000423479 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:46914606 C>T maps to NM_032040.3 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr11:62301276 G>A maps to NM_001620.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:949845 C>T maps to NM_005101.3 G162G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chrX:13727113 C>T maps to NM_004251.4 C83C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:9804387 G>A maps to NM_002903.2 D137D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:6294998 G>A maps to NM_012405.3 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:208390532 G>A maps to NM_025179.3 Y245Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:15254958 C>T maps to NM_001010924.1 W876*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:34893858 C>T maps to NM_178517.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:109526136 G>A maps to NM_001145375.1 H220H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:179440958 C>T maps to NM_133378.4 Q20732Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:35770247 G>A maps to ENST00000400445 T1725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:10448738 G>A maps to NM_017534.5 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:148924001 G>T maps to NM_000096.3 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:7645693 T>C maps to NM_019005.3 S841S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:37035643 G>A maps to NM_053276.3 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:66600559 C>T maps to NM_052999.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:136605707 G>T maps to NM_005915.4 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr6:151686670 G>A maps to NM_020861.1 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:116930356 C>T maps to NM_032888.2 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:84600555 G>A maps to NM_021149.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:220439862 G>A maps to NM_002191.3 W239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:57876616 A>C maps to NM_000938.1 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:11505705 C>T maps to NM_001080491.2 A424A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:25672096 A>G maps to NM_030979.2 E587E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:51748528 C>T maps to NM_001077665.2 D18D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:248343967 C>T maps to NM_001004688.1 H227H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr20:18005393 C>T maps to NM_021220.2 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:33625512 G>A maps to NM_018207.2 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:106858223 C>T maps to ENST00000503451 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:104068647 C>T maps to NM_001813.2 L1333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:30776080 C>T maps to NM_001017981.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:120791156 G>T maps to NM_002442.2 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:226109029 G>A maps to NM_013328.2 C225C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:84438756 G>A maps to ENST00000416219 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:117849132 G>A maps to NM_002160.2 R293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:73035038 A>G maps to NM_006356.2 I158I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:146058590 C>T maps to ENST00000447906 Q1112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:70744218 C>T maps to NM_030958.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr11:70031719 G>A maps to NM_018043.5 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:62492846 A>G maps to NM_007215.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:80788497 C>T maps to NM_024702.2 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chrX:19037718 C>T maps to NM_001079858.2 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:123699208 G>A maps to ENST00000484329 Y40Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:112579784 G>A maps to NM_152556.2 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:1271164 C>T maps to ENST00000413636 Q44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr9:112145795 G>A maps to NM_002829.3 D763D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr15:90763059 G>A maps to NM_198925.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:178952025 C>A maps to NM_006218.2 A1027A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr11:56310190 C>T maps to NM_001005245.1 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr14:47504409 T>C maps to NM_001113498.2 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:80016029 T>G maps to NM_022156.3 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:149133689 G>A maps to ENST00000440594 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:17400869 C>T maps to NM_001164771.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr18:43248312 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:70934963 C>T maps to NM_032821.2 L2996L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:28285051 C>T maps to NM_014474.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:74467834 G>A maps to NM_024599.5 A817A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:186009010 G>A maps to NM_031935.2 Q2060Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:52526218 C>T maps to NM_007184.3 R1412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:95034756 G>A maps to NM_005708.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:113849440 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:92789301 C>T maps to NM_024813.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr15:82336337 C>T maps to NM_032246.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:133976843 C>A maps to NM_001105521.2 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr15:59179239 G>A maps to NM_024755.2 S923S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr14:95571439 G>A maps to NM_177438.2 G1079G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr11:108068118 A>G maps to NM_002519.2 S22S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:6695685 C>T maps to NM_005980.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr6:165715063 C>T maps to NM_144980.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:102737390 G>A maps to NM_017893.2 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:241468860 G>A maps to ENST00000401804 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:13325396 G>A maps to NM_023035.2 D1923D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:119303005 G>A maps to NM_004098.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr5:140431843 G>A maps to NM_013340.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr14:22133361 G>A maps to NM_001001912.1 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:38038578 C>A maps to NM_015873.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:110603474 G>A maps to NM_006492.2 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr15:56735680 G>A maps to NM_018365.2 R320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:1106406 C>T maps to NM_002085.3 I170I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr18:60241836 C>T maps to NM_017742.4 I841I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:56435188 G>A maps to NM_017763.4 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:33344574 G>A maps to NM_001017368.1 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:110763517 C>T maps to NM_018334.4 N230N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:6634740 C>A maps to NM_138697.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:28014242 G>A maps to NM_152912.4 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:234237187 C>T maps to NM_000541.4 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:159711353 G>A did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:235416113 G>A maps to NM_016374.5 D95D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:19748734 C>A maps to NM_016573.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr7:100280925 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:10392201 G>A maps to NM_001001331.2 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr4:4239661 G>A maps to ENST00000382753 C133C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr16:67264378 G>A maps to NM_013241.2 Y963Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr13:39261855 G>A maps to NM_207361.4 K125K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:159860403 G>C maps to NM_012337.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr14:35255347 C>T maps to NM_013448.2 W530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:16534047 G>A maps to NM_153213.3 N281N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:14746119 C>T maps to NM_032137.4 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:39879988 G>A maps to NM_019088.2 R132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:49169814 C>T maps to NM_015270.3 G579G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:30416461 C>A maps to NM_021090.3 A938A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr2:234371287 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr3:49759675 G>A maps to NM_013334.2 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr11:129800949 C>T maps to NM_020228.2 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr19:2222179 C>T maps to ENST00000221482 H1004H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:12017969 C>T maps to ENST00000376369 D318D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr10:93768863 G>A maps to NM_003972.2 P1334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr1:153516336 G>A maps to NM_002961.2 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr12:60098740 T>C maps to NM_004731.3 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:1543258 G>T maps to NM_003693.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr22:42423016 C>A maps to NM_152613.2 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:7224436 G>A maps to NM_032442.2 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr17:48703835 C>T maps to NM_018896.3 D2286D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr18:33739978 G>T did not map to a codon.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr14:103807367 C>T maps to NM_183004.3 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr6:136990478 C>A maps to NM_005923.3 A436A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr15:74467873 G>A maps to NM_201526.1 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr5:149755038 G>A maps to ENST00000451292 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr5:94848277 C>T maps to NM_014639.3 L941L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr19:35718887 G>A maps to NM_152481.1 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr1:180885313 A>G maps to NM_020950.1 T25T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr16:703784 G>A maps to NM_145294.4 K473K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr19:54395834 C>T maps to NM_002739.3 N253N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr1:27874813 C>T maps to NM_001029882.2 P1271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr10:105361686 C>A maps to ENST00000369774 V1096V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7783-01A-11D-2114-08 chr17:39871694 C>T maps to NM_000805.3 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr5:82499424 G>T maps to NM_022406.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr5:139887387 T>A maps to ENST00000253810 G1190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr3:168834357 C>G maps to NM_004991.3 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr1:223163993 G>A maps to NM_032890.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr15:50212486 C>A maps to NM_024837.2 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr16:67859050 G>T maps to ENST00000339830 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr2:75879652 T>C maps to NM_014763.3 S115S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr12:6858043 G>A maps to NM_005439.2 R222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr11:55607136 C>T maps to NM_001005496.1 R304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr3:120130763 G>A maps to NM_007085.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr16:3487539 T>G did not map to a codon.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr12:112572541 C>A maps to NM_006700.2 C16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr6:87966665 C>T maps to NM_015021.1 R1107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr1:64022883 G>A maps to NM_032437.2 E438E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr22:24381722 G>A maps to NM_000853.2 D59D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr19:50245230 G>A maps to NM_021733.1 R470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr16:3306385 G>A maps to NM_000243.2 Q68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr3:186299281 C>T maps to NM_016306.4 C193C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr19:16688031 G>T maps to NM_004831.3 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr3:52402840 G>A maps to ENST00000273600 P1950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr9:113704387 G>A maps to NM_057159.2 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr6:34498307 G>A maps to NM_020804.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7784-01A-11D-2114-08 chr1:248458841 T>C maps to NM_001004692.1 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr6:129824262 C>T maps to NM_000426.3 T2795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr17:54558082 G>A maps to NM_153228.2 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chrX:48054233 G>A maps to NM_021015.3 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr1:36028871 G>T maps to NM_001014839.1 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr7:100681500 C>T maps to NM_001040105.1 S2268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr15:42162705 G>A maps to ENST00000320955 R1834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7785-01A-11D-2114-08 chr1:21205815 C>G maps to NM_001198801.1 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr3:150932017 G>A maps to NM_014879.3 Y29Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr6:157528682 G>A maps to ENST00000367148 S2176S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chrX:131188792 A>G maps to ENST00000481105 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr1:78194271 G>A maps to NM_015017.3 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr1:154173059 G>A maps to NM_001010979.1 R27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr11:70336435 T>G maps to ENST00000338508 P826P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr15:65622152 C>T maps to NM_004884.3 T636T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr5:135392371 C>A maps to NM_000358.2 I522I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr2:163279881 G>A maps to NM_033272.2 H706H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr4:128818020 G>T maps to NM_014264.4 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr14:23395505 C>G did not map to a codon.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr11:6977518 C>T maps to NM_013250.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr16:67694961 T>C maps to NM_016948.2 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chrX:153046770 G>T maps to NM_014370.3 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr12:55794776 T>C maps to NM_001005518.1 F155F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7786-01A-11D-2114-08 chr1:21040006 C>G maps to NM_020816.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr11:83243768 T>C maps to NM_001142699.1 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr11:75150997 G>A maps to NM_030792.6 D494D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr3:188327154 G>T maps to NM_005578.3 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr20:52779273 C>T maps to NM_000782.4 Q324Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr14:23587879 G>A maps to NM_001805.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr1:5964710 G>A maps to NM_015102.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr16:1709960 G>A maps to NM_020825.3 G770G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr19:10670557 C>T maps to NM_023008.3 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr9:90252884 C>T maps to NM_004938.2 F104F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr20:52779276 G>T maps to NM_000782.4 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr20:50244192 C>A maps to NM_006045.1 R597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr18:9522267 C>T maps to NM_006788.3 R272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr11:89028438 C>T maps to NM_000372.4 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7788-01A-11D-2114-08 chr3:69075247 C>A maps to NM_007114.2 E920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr6:37426393 C>T maps to NM_015050.2 L262L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr19:9057079 G>T maps to NM_024690.2 I10122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr6:10928670 C>T maps to NM_001040274.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr4:110972802 T>C maps to NM_024090.2 G163G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr1:248201937 G>T maps to NM_001004686.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr1:89319012 A>T maps to NM_001514.5 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr15:43620820 A>G maps to NM_014793.4 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7789-01A-11D-2114-08 chr7:91870305 C>T did not map to a codon.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr2:198353197 A>G maps to NM_199440.1 D411D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr8:103298846 T>C did not map to a codon.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr3:38835294 C>T maps to NM_006514.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr7:28527794 T>C maps to NM_182898.2 I2I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr15:41804905 G>A maps to NM_002344.5 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr7:143013472 C>A maps to NM_000083.2 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr14:24661452 C>T maps to NM_006405.5 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7791-01A-11D-2114-08 chr1:23520100 C>T maps to NM_000864.4 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7792-01A-11D-2114-08 chr19:6743804 C>T maps to ENST00000313244 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7792-01A-11D-2114-08 chr22:20082237 C>T maps to NM_022720.6 R570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7792-01A-11D-2114-08 chr3:44684196 C>T maps to NM_006991.3 L525L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr10:85972117 C>T maps to NM_033100.2 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr12:32903752 G>A maps to NM_001040436.1 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr8:89128876 C>T maps to NM_005941.4 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr15:50833425 T>C maps to ENST00000456636 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7793-01A-31D-2260-08 chr19:18543389 G>A maps to NM_032627.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr19:46334799 C>T maps to NM_004819.2 K480K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr8:22880192 G>T maps to NM_003842.4 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr7:121651646 C>T maps to NM_002851.2 T849T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr12:15742394 C>T maps to NM_030667.1 G1139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr9:133779561 G>A maps to NM_001145106.1 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7794-01A-11D-2114-08 chr7:138145409 G>A maps to NM_015905.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr1:9931302 G>A maps to ENST00000361853 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr16:67876807 G>A maps to NM_020457.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr4:126242059 C>G maps to NM_024582.4 A1498A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr3:71096125 G>A maps to NM_032682.4 Q211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr3:71096126 C>A maps to NM_032682.4 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr4:5735119 C>T maps to NM_153717.2 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr18:21492719 C>T maps to ENST00000416669 R2404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr6:32010243 C>G maps to ENST00000375244 G4066G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7797-01A-11D-2260-08 chr3:32800948 G>C did not map to a codon.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr14:38061622 G>A maps to NM_004496.2 A122A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr17:61432334 C>A maps to ENST00000389520 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr15:65041628 C>T did not map to a codon.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr15:43821146 C>A maps to ENST00000382031 C2730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr15:78471896 C>G maps to NM_015162.4 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr8:99440248 C>A maps to NM_020697.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr2:233323609 G>A maps to NM_001631.3 S447S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr19:9453236 A>G maps to NM_032497.1 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr22:30416350 G>A maps to NM_021090.3 R901R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8468-01A-21D-2395-08 chr17:58529352 A>G maps to NM_006380.2 G464G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr3:183667863 G>A maps to NM_005688.2 I998I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chrX:106171820 T>G maps to NM_001171095.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr5:177419760 T>G maps to NM_006261.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr17:34912922 C>T maps to NM_024835.3 R59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr17:42340028 G>A maps to NM_000342.3 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr11:92086738 G>A maps to ENST00000298047 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr17:6503778 C>T did not map to a codon.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr12:121435349 C>T maps to NM_000545.5 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr5:75490816 A>G maps to NM_014979.1 K218K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr17:79657218 C>A maps to NM_004712.4 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr5:140229646 T>C maps to NM_031857.1 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr22:38121844 C>T maps to NM_001039141.2 A1094A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr14:24877238 C>T maps to NM_025081.2 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr8:144398198 G>A maps to NM_052963.1 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr14:23828663 T>G maps to NM_005864.2 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr14:23828669 T>G maps to NM_005864.2 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8469-01A-11D-2395-08 chr9:99013717 G>A maps to NM_000197.1 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr10:101373522 G>A maps to NM_031212.3 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr10:75139866 G>A maps to NM_004034.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr12:47472524 C>T maps to NM_001143668.1 W87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr12:41316216 C>A maps to NM_001843.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr8:117783945 T>A maps to NM_032334.2 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr18:13826201 C>T maps to NM_005913.2 Y146Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr16:4780009 C>T maps to NM_133450.2 Q47Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8470-01A-11D-2395-08 chr16:20952768 C>A maps to NM_017539.1 E3870*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chrX:113965912 G>A maps to NM_000868.2 K82K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr5:175933900 G>T maps to NM_014613.2 G430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr16:75513510 G>A maps to NM_021615.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr5:123984771 C>A maps to NM_020747.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr1:247921333 C>T maps to NM_012353.2 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr6:170175419 G>T maps to NM_018341.1 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chrX:144906345 C>T maps to NM_001144010.2 T801T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr19:41626274 C>T maps to NM_000774.3 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr6:7229900 G>C maps to NM_001003699.3 T523T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr5:121776373 G>A maps to ENST00000379533 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr15:54306248 C>G maps to ENST00000260323 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr1:67724720 C>T maps to NM_144701.2 I600I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr10:96827285 C>A maps to NM_000770.3 G111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr17:8215725 G>A maps to NM_173728.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8472-01A-11D-2395-08 chr8:110420308 T>A maps to ENST00000426474 V615V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr8:19682475 C>T maps to NM_018142.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr11:5686408 C>T maps to NM_033034.2 W371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr2:19553371 C>T maps to NM_145260.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr7:91667794 A>G maps to NM_005751.4 G1467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr1:16534594 A>G maps to NM_153213.3 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr14:75367845 G>A maps to NM_001933.4 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr1:45253306 C>T maps to NM_153274.2 W24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr16:67264086 G>A maps to NM_013241.2 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr2:167133600 G>A maps to ENST00000303354 R923R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr13:95862990 G>C maps to NM_005845.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr11:6048226 T>C maps to NM_001001917.2 K236K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr8:133925307 C>T maps to NM_003235.4 G1392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr1:157666076 G>A maps to NM_052939.3 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr7:113518487 C>A maps to NM_002711.3 E887*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr1:114201720 C>T maps to NM_001142782.1 G883G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr4:83280637 C>A maps to NM_031370.2 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr22:47095219 G>A maps to NM_022766.5 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chrY:4925415 G>A maps to NM_032973.1 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chrX:1401454 T>G did not map to a codon.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr19:38876986 A>G maps to NM_152657.3 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr8:145773443 G>A maps to NM_025251.1 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr4:79792151 C>T maps to NM_198892.1 Q483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr16:5038193 G>A maps to NM_014692.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr3:123456318 G>T maps to NM_053025.3 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46B-01A-31D-A257-08 chr3:63981654 C>T maps to NM_001177387.1 S719S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr6:87726041 G>A maps to NM_000865.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr19:40901384 C>T maps to NM_181882.2 K958K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr6:143780271 G>T maps to NM_003630.2 E42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr3:50005400 T>C maps to NM_005777.2 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46D-01A-21D-A257-08 chr2:234527190 G>T maps to NM_019076.4 G280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46E-01A-31D-A257-08 chr7:92764068 G>A maps to NM_152703.2 R406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46E-01A-31D-A257-08 chr3:58062899 G>A maps to NM_001164317.1 T140T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr2:225684222 T>G maps to NM_014689.2 R1069R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr7:111503617 A>T maps to ENST00000428084 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr3:157154781 G>A maps to NM_002852.3 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr19:17999205 C>T maps to NM_000453.2 Y531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr19:1986927 G>A maps to NM_017797.3 G439G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr19:9058118 G>C maps to NM_024690.2 S9776*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr7:100683804 A>T maps to NM_001040105.1 I3036I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr10:16882352 G>C maps to NM_001081.3 Y3336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr11:19213896 C>T maps to NM_003476.3 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr13:23912524 C>T maps to NM_014363.4 L1830L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr17:15134174 T>G did not map to a codon.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr1:154938796 A>G maps to NM_001130040.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr14:42356736 G>A maps to NM_152447.3 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr1:203138380 C>T maps to NM_004997.2 K410K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr22:26761443 C>T maps to NM_021115.4 Y902Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46F-01A-31D-A257-08 chr8:135612747 G>A maps to NM_020863.3 T802T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr11:67074409 G>T maps to NM_017857.3 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr16:56398014 G>A maps to NM_001144.4 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr6:16146915 T>A maps to NM_013262.3 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr2:99182211 C>T maps to NM_001134224.1 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr3:47455418 G>A maps to NM_012235.2 N1255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr3:13393390 C>T maps to NM_024923.2 R941R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr13:39451251 A>G did not map to a codon.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr19:11453690 G>T maps to NM_198536.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr15:26026297 G>A maps to NM_024490.3 N174N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr6:31911053 C>T maps to ENST00000437789 N318N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr1:160394000 G>A maps to NM_020335.2 Q411Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr4:47527618 G>T maps to NM_020453.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr20:61525241 G>A maps to NM_033081.2 T959T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr2:179399092 T>C maps to NM_133378.4 K31515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr2:189859301 C>T maps to NM_000090.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr3:130284216 C>T maps to NM_001102608.1 N347N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr8:77617576 C>A maps to NM_024721.4 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr8:132051760 G>A maps to NM_001115.2 Y273Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr8:42611139 G>T maps to NM_004198.3 S401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr3:135913889 G>T maps to NM_018133.3 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr2:160050844 C>T maps to NM_033394.2 C940C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr18:29218611 C>A maps to NM_004775.3 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr1:161166337 G>C maps to ENST00000367995 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr11:4566998 C>T maps to NM_001004137.1 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr8:22275305 G>A maps to NM_001135153.1 A430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr17:8079028 G>C maps to ENST00000417073 S101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A46I-01A-12D-A26M-08 chr15:33941373 C>T maps to NM_001036.3 D1360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chrX:3573440 C>T maps to NM_005044.4 W116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr6:146125918 A>C maps to NM_032145.4 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr12:82746932 A>G maps to NM_014167.4 C241C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr1:235647822 G>A maps to ENST00000366599 Q165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chrX:39911628 C>T maps to NM_001123385.1 S1667S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr10:105330663 C>A maps to NM_004210.4 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr12:40689227 G>A did not map to a codon.
Sequencing variant TCGA-EJ-A65B-01A-12D-A30E-08 chr16:16256865 G>A maps to NM_001171.5 R1164*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr1:9011713 C>T maps to ENST00000319474 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr7:82544134 C>T maps to NM_033026.5 R4389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr11:1263452 G>A maps to ENST00000447027 T1784T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr12:7531633 G>A maps to ENST00000416109 R781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr1:12907827 G>A maps to NM_001013631.1 Y105Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr9:125551978 C>T maps to NM_001001923.1 Y256Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr15:53889438 C>T maps to NM_182758.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65D-01A-11D-A30E-08 chr15:54804027 G>A maps to ENST00000260323 E1819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr11:56949993 C>T maps to NM_001005210.2 D209D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr21:41551003 G>A maps to NM_001389.3 Q933*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr1:62718879 G>T maps to NM_181712.4 G847G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr6:43267186 C>T maps to ENST00000372585 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr19:49653358 G>C maps to NM_003660.2 R1183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr12:1943628 G>A maps to NM_001163926.1 P285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr1:1722001 C>T maps to NM_002074.2 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr1:145441199 C>T maps to NM_006472.3 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr2:162804173 T>C maps to NM_001178015.1 F734F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr1:205897956 G>A maps to NM_134325.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr6:152647579 G>A maps to NM_182961.2 N5048N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr7:103341382 C>T maps to ENST00000428762 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr12:109523651 G>T maps to NM_032663.3 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65E-01A-11D-A29Q-08 chr3:100287664 G>C did not map to a codon.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr19:56482026 G>A maps to NM_176811.2 A833A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr22:36696286 C>T maps to NM_002473.4 E954E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr15:66821853 G>A maps to NM_017975.3 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr4:104577478 G>A maps to NM_001059.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:154067629 A>T maps to NM_207308.2 A656A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr19:10398290 G>T maps to NM_001544.3 V158V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr16:53190624 C>T maps to ENST00000219084 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr12:117660555 C>T maps to ENST00000338101 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr22:42377715 G>A maps to NM_145733.2 A26A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:114499302 C>T maps to ENST00000426820 R559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr17:16285559 T>C maps to NM_018955.2 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr20:60737904 C>A maps to NM_198935.1 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr14:23522820 C>T maps to NM_022478.3 E370E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr10:127730775 G>A maps to NM_021641.3 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr8:70585421 G>A maps to NM_030958.2 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr9:104432659 C>T maps to NM_133445.2 W678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr15:75941790 C>T maps to NM_153271.1 D116D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:207133069 A>G maps to NM_001170631.1 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:203690538 G>A did not map to a codon.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr8:55059976 G>T maps to NM_014175.3 G197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr8:124195407 C>A maps to NM_032899.4 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr1:206858780 C>G maps to NM_032960.2 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr15:54792333 A>G maps to ENST00000260323 E1706E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr14:93709032 A>T maps to NM_001002860.2 G995G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr3:48474342 C>T maps to NM_024661.3 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr6:143092406 G>A maps to NM_006734.3 Q1157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr10:101503042 T>A maps to NM_015960.2 Y109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chrX:120008935 G>A maps to NM_001145718.1 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr3:121208387 A>G maps to ENST00000393672 N1266N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr12:109894045 G>C maps to NM_031954.3 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr6:33284251 G>A maps to NM_001145338.1 R148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr1:91182527 C>A maps to NM_020063.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr13:28794429 C>T maps to NM_175854.7 N305N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65G-01A-21D-A29Q-08 chr9:33385584 C>A did not map to a codon.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr11:62554329 A>T maps to NM_006473.2 A477A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr8:26628172 G>A maps to ENST00000356368 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr22:38340507 C>T maps to NM_032561.3 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr15:45968453 A>G maps to NM_021199.2 K270K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:49797194 G>A maps to NM_014037.2 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr3:13659705 C>T maps to NM_001165035.1 C620C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr10:64573203 G>A maps to NM_001136178.1 F398F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:56733189 G>A maps to NM_024303.1 D415D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr12:56078883 G>A maps to ENST00000347027 P1168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr6:54216176 C>T maps to NM_014464.3 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:35753474 C>T maps to NM_205834.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr5:150444611 G>A maps to NM_006058.3 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:4523866 G>A maps to NM_001013706.2 H355H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65J-01A-11D-A30X-08 chr19:44099418 G>A maps to NM_001007561.2 I24I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr6:56373516 C>T maps to ENST00000361203 W6139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr22:39917542 A>G maps to NM_182810.1 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr10:47000208 C>T maps to NM_014696.3 S443S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr5:140563339 C>A maps to NM_020957.1 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr4:84015881 G>T maps to NM_001130715.1 I102I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr19:40715126 G>A did not map to a codon.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr8:145109714 C>T maps to ENST00000360660 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr4:39448817 C>T maps to NM_175737.3 N824N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr12:100166697 A>G did not map to a codon.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr6:152469435 C>T maps to NM_182961.2 W8240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr10:64968221 A>G maps to NM_032776.1 D1069D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr20:58514329 C>T maps to NM_006242.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr1:92944267 T>G maps to NM_005263.3 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-A65M-01A-11D-A29Q-08 chr1:242511505 G>A maps to NM_152666.2 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr1:167973819 T>C maps to ENST00000367840 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr6:43023653 G>A maps to NM_015950.3 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr8:101612648 T>C maps to NM_152628.3 K234K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr12:58002361 G>A maps to NM_178502.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr4:146058890 A>C maps to ENST00000447906 V1012V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr1:161479820 C>A maps to NM_001136219.1 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr2:98351130 C>T maps to NM_001079.3 C346C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr2:192863885 G>A maps to NM_016192.2 C195C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr15:62320581 G>A maps to NM_020821.2 N141N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr6:94120324 C>T maps to NM_004440.3 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr19:36728179 A>T maps to NM_007145.2 K280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr9:71395166 C>G maps to NM_138333.3 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7708-01A-11D-2114-08 chr3:38766806 T>C did not map to a codon.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:201453912 A>G maps to NM_001193572.1 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr5:55422828 C>T maps to NM_024669.2 A239A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr19:57065053 C>G maps to NM_020828.1 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr8:143558526 C>T maps to NM_001702.2 C370C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr2:242039185 C>A maps to NM_182501.3 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr6:38545496 T>A did not map to a codon.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr11:106810482 C>T maps to ENST00000282249 K303K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr12:53509946 C>T maps to NM_003578.3 R259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr10:128973612 G>A maps to NM_001039762.2 I349I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr6:29627138 G>C maps to NM_002433.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:158605701 C>A did not map to a codon.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr9:5185353 C>T maps to NM_007179.2 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr8:25341515 A>C maps to ENST00000434814 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:153732835 C>A maps to ENST00000428986 I430I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr5:140531640 G>A maps to NM_018939.2 S601S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr14:62233592 G>T did not map to a codon.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr9:134889830 T>C maps to NM_004269.2 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chrX:24075811 T>C maps to NM_001415.3 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-7961-01A-11D-A29Q-08 chr1:152857071 C>T maps to NM_030663.2 C58C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr18:74620422 A>G maps to NM_007345.3 A813A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr19:54444868 G>A maps to NM_031896.4 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr10:128973672 C>T maps to NM_001039762.2 P329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr2:145156430 A>G maps to NM_014795.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr2:170068628 G>A maps to NM_004525.2 C2043C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr4:3234975 C>T maps to NM_002111.6 H2784H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr6:135787208 G>A maps to NM_017651.4 G164G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr15:43701248 G>A maps to NM_001141980.1 R1816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr2:69092996 G>A maps to NM_014482.1 Y347Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr1:75805313 A>G maps to NM_152697.4 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr2:80530542 C>T maps to NM_178839.4 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr17:66519942 T>C maps to NM_212472.1 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr6:38820471 G>A maps to ENST00000327475 P1811P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr6:54186158 G>T maps to NM_014464.3 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr14:105414143 G>A maps to NM_138420.2 D2548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr6:52268631 C>T maps to ENST00000361841 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr1:150255958 G>A maps to NM_144697.2 A94A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr3:20215803 T>G maps to NM_001012410.3 R407R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr11:133814171 G>A maps to NM_014987.1 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr16:1537737 C>T maps to NM_001013658.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr17:15207264 G>A maps to NM_031898.2 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr13:103701636 A>G did not map to a codon.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr17:72858968 A>C maps to ENST00000442102 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chrX:49072960 T>G maps to NM_005183.2 G1050G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr7:99474461 C>T maps to NM_001005276.1 Q65Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr7:130357703 G>A maps to NM_052933.2 Q134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr9:3828280 G>A maps to NM_001042413.1 T928T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr12:57112271 C>T maps to NM_001113203.1 V1014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr15:40501920 G>A maps to ENST00000412359 L757L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr6:52268841 C>A maps to ENST00000361841 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A5OB-01A-11D-A29Q-08 chr19:35793405 G>A maps to NM_002361.3 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A66V-01A-21D-A30E-08 chr22:29628272 C>T maps to NM_133455.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A66V-01A-21D-A30E-08 chr14:38060701 G>A maps to NM_004496.2 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr7:143806867 C>T maps to NM_001005480.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr3:196460769 A>G maps to NM_001166304.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr7:23300354 A>G maps to ENST00000435486 P362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr18:46447810 G>A maps to NM_005904.3 G404G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr14:24880386 G>A maps to NM_025081.2 Q840Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr17:39912082 G>A maps to NM_021991.2 H717H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr14:52735164 C>T maps to NM_000953.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr5:140563060 C>T maps to NM_020957.1 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr1:78959036 A>C maps to NM_000959.3 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr4:37591964 C>T maps to NM_018302.2 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr12:118474219 G>C maps to ENST00000441406 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr3:12783980 A>G maps to ENST00000431022 V111V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A6HD-01A-11D-A31L-08 chr19:8188378 G>A maps to NM_032447.3 F1017F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr8:22472958 G>A maps to NM_021174.5 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr2:137814554 G>T maps to ENST00000272643 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr3:101384240 G>C maps to NM_014415.3 S397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr6:90426385 G>A maps to NM_014611.1 D2242D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr16:23716454 C>T maps to NM_033266.3 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr20:62320907 G>T maps to ENST00000482936 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr17:77809098 C>T maps to NM_003655.2 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr11:60666068 C>A maps to NM_014502.4 G362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr10:102048746 G>A maps to NM_016112.2 Q773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr4:148407184 C>T maps to NM_001957.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr16:21109951 C>T maps to NM_017539.1 A835A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6329-01A-13D-1961-08 chr8:61736613 G>C maps to ENST00000453098 *1139Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:17409275 G>A maps to NM_000525.3 F121F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:111737240 G>A maps to NM_024901.3 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr19:48533839 C>T did not map to a codon.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr6:1611153 C>T maps to NM_001453.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr11:67052767 G>A maps to NM_001619.3 E639E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr10:13375854 T>C maps to NM_012247.4 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr15:86838595 G>A maps to NM_152336.2 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6332-01A-11D-1786-08 chr1:168698283 C>T maps to NM_001937.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr15:95013612 G>A maps to NM_018349.3 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr7:141351366 G>A maps to NM_018238.3 T363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr19:2421892 C>T maps to NM_182973.1 G698G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:237711847 G>A maps to NM_001035.2 A1008A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:165370514 C>T maps to NM_006917.4 P459P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:200972743 C>T maps to NM_017596.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr17:76803038 A>C did not map to a codon.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr10:104866419 A>C maps to NM_001134373.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr21:47423617 C>T maps to NM_001848.2 F926F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr10:67680275 G>A maps to NM_013266.2 R834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr3:154861329 A>G maps to NM_007289.2 E429E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr1:228433201 G>C maps to NM_001098623.1 V1190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr17:37074902 G>T maps to NM_006148.2 E220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6333-01A-12D-1961-08 chr8:139890293 G>A maps to NM_152888.1 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr5:145890176 C>A maps to NM_006706.3 S1090*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr8:52320733 G>T maps to NM_144651.4 I1150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr13:114780694 C>T maps to ENST00000389544 K472K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr16:74336162 G>A maps to NM_002811.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr11:110450381 C>T maps to NM_020809.2 R1096R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr7:131172447 T>G maps to NM_013255.4 T723T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6336-01A-11D-1786-08 chr17:48270009 G>A maps to NM_000088.3 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr6:39158872 G>A maps to NM_003740.3 D431D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr5:140502261 C>T maps to NM_018938.2 R228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr16:1961821 G>A maps to ENST00000454677 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr10:37508446 T>G maps to ENST00000374660 Y1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr7:107880412 T>C maps to ENST00000379032 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr10:71877571 C>A maps to NM_032797.5 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr4:3176834 G>C did not map to a codon.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr7:158443615 G>A maps to NM_017760.5 Q995*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr15:43748752 T>A maps to NM_001141980.1 K685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6338-01A-12D-1961-08 chr3:73016752 C>T maps to NM_001080393.1 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr12:96641091 C>T maps to NM_005230.2 V194V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr7:150761317 G>A maps to NM_003040.3 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr19:19790541 T>C maps to NM_033204.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr2:99725895 G>A maps to NM_025244.2 R3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr1:27674031 G>A maps to NM_001193308.1 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr14:102482729 C>T maps to NM_001376.4 S2506S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr16:31372439 G>A maps to NM_000887.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr2:139318403 T>C maps to NM_001001664.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr18:31802971 G>T maps to NM_003787.4 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr22:40066134 C>T maps to NM_021096.3 V1429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr1:152279918 C>T maps to NM_002016.1 L2481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr1:229577701 G>A maps to NM_018230.2 F1140F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr5:159476555 T>C maps to NM_003314.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6339-01A-12D-A30X-08 chr19:17370704 C>T did not map to a codon.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr4:128626837 A>G maps to NM_015693.3 K553K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:185931776 C>T maps to NM_031935.2 I652I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr5:39311237 C>T did not map to a codon.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:205132934 G>A maps to NM_015375.2 F491F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:132874313 G>A maps to NM_053278.1 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chrX:153073954 G>A maps to ENST00000393758 R52R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr1:196254843 C>T maps to NM_198503.2 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr6:145093096 A>G maps to NM_007124.2 Q2850Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr4:114275161 C>T maps to NM_001148.4 D1796D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6342-01A-11D-1961-08 chr3:122459554 G>A maps to NM_024610.4 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr1:34684352 A>C maps to NM_001134734.1 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr6:150569955 A>C maps to NM_030949.2 *166C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr3:178952049 T>G maps to NM_006218.2 A1035A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr7:99096408 G>A maps to NM_032164.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr1:35226968 G>A maps to NM_153212.2 V38V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr12:70925904 G>A maps to NM_001109754.1 I2138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr10:35929634 C>A maps to NM_031866.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr19:9087659 G>A maps to NM_024690.2 T1385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr22:37263491 C>T maps to NM_013416.3 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr22:39626110 C>T maps to NM_002608.2 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr2:50850691 T>C maps to ENST00000404971 Q331Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr19:17265123 G>A did not map to a codon.
Sequencing variant TCGA-G9-6343-01A-21D-1961-08 chr12:94763797 T>C maps to NM_001042399.1 K316K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr2:219825270 C>T maps to NM_003936.3 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr14:30100143 G>A maps to NM_002742.2 F492F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr2:136481597 C>T maps to ENST00000409606 G1013G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr2:26203358 C>T maps to NM_002254.6 Q476Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr3:123383036 C>T maps to NM_053025.3 A1300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr16:2142145 C>T maps to NM_001009944.2 S3771S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr3:38627373 G>A maps to NM_001099404.1 Y865Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6347-01A-11D-A31L-08 chr20:61288285 C>T maps to NM_016354.3 V160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr11:65315006 G>A maps to NM_001130144.2 C670C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:10355524 G>A maps to NM_017533.2 A1157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:149885275 G>A maps to NM_014849.3 D39D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr16:54966501 A>G maps to NM_005853.5 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr9:139701516 C>A maps to NM_001039374.4 I495I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:167142944 C>T maps to ENST00000303354 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:61949662 G>A maps to NM_020991.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr22:43267419 G>A maps to NM_001184970.1 R468R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr15:63632618 G>A maps to NM_001218.3 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr17:42333172 G>A maps to NM_000342.3 N556N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr4:175897857 C>T maps to NM_014269.4 I394I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr6:168297652 G>T did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr15:28386774 G>A maps to NM_004667.4 R3940*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr6:130762196 C>A maps to NM_052913.2 I210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr10:26575383 C>T maps to NM_001134366.1 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:12058936 T>A did not map to a codon.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:161022537 T>C maps to NM_001025598.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:51255225 G>A maps to ENST00000404971 S62S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr2:167262809 A>T maps to NM_002976.2 I1443I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6348-01A-11D-1786-08 chr1:175086261 G>A maps to NM_022093.1 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr21:42839792 C>T maps to NM_001135099.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:146765329 T>C maps to NM_004284.3 N810N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr5:31323129 C>A maps to NM_004932.2 A696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr15:91524743 T>C maps to NM_003981.2 Q219Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr1:153122526 C>T maps to NM_001014291.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6351-01A-21D-1961-08 chr19:16040399 C>A maps to NM_021187.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6353-01A-11D-1961-08 chr22:37524347 G>A maps to ENST00000406505 L487L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6353-01A-11D-1961-08 chr9:34343326 C>T maps to NM_147173.1 H111H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6353-01A-11D-1961-08 chr1:45296669 C>T maps to NM_003738.4 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr1:160654875 G>A maps to NM_001778.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr14:24702731 C>A maps to ENST00000348719 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr6:151054999 G>A maps to NM_001029884.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr8:72973924 C>T maps to NM_007332.2 S293S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr4:26622267 T>A maps to NM_018317.2 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr3:180359821 C>T maps to NM_181426.1 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr6:45390444 A>G maps to ENST00000359524 Q126Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr3:49136842 G>A maps to NM_005051.1 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr4:56768604 A>G maps to NM_018261.3 K811K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr20:62126424 C>T maps to NM_001958.2 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr15:98995216 G>A maps to NM_182562.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6354-01A-11D-A30X-08 chr12:69103088 G>A maps to NM_020401.2 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr8:24199260 C>T maps to NM_014265.4 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr12:72036213 A>C did not map to a codon.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr11:132081913 A>C did not map to a codon.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr14:76224210 C>T maps to ENST00000286653 R68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr1:227842074 C>T maps to NM_178549.3 Q97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr21:34903823 C>A maps to NM_001136006.1 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr15:42446633 C>T maps to ENST00000397272 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr2:70130360 C>T maps to NM_006857.1 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr12:6686949 C>T did not map to a codon.
Sequencing variant TCGA-G9-6356-01A-11D-1786-08 chr5:648007 G>A maps to NM_018140.3 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chrX:151514067 G>A maps to NM_000808.3 R83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr8:139209801 C>T maps to NM_015912.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr12:53878998 C>G did not map to a codon.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr12:52200654 C>T maps to NM_014191.2 F1795F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr11:120008220 G>A maps to NM_012101.3 C173C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr19:55687184 C>T maps to NM_003180.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr1:207040804 T>C did not map to a codon.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr15:74219534 G>C maps to NM_005576.2 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr11:66812167 C>T maps to NM_001177880.1 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr17:46048773 G>T did not map to a codon.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr13:100518572 C>A maps to NM_206808.2 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6361-01A-21D-1961-08 chr4:48611010 G>A maps to NM_015030.1 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr12:113748107 G>T maps to NM_024959.2 I396I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:26033604 C>T maps to NM_003513.2 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:130854175 A>G maps to ENST00000373066 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr3:107096616 C>T maps to NM_032600.2 D61D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr17:34249536 T>G maps to NM_001034836.1 *237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:16465317 T>A maps to NM_033414.2 K153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr17:77768835 C>T maps to NM_020649.2 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:140711177 C>T maps to NM_018912.2 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:123171435 C>A maps to NM_018249.4 E1525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:35579020 A>G maps to NM_024772.3 Q530Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr14:74426129 T>C maps to NM_182476.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:115454197 C>T maps to NM_003176.2 N508N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr2:179412021 G>A maps to NM_133378.4 S28842S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:51915070 C>T maps to NM_138694.3 T721T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:1271545 G>A maps to ENST00000378888 C688C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr19:44103049 T>C maps to NM_024327.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr11:55999740 C>T maps to NM_001004746.1 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:158390383 G>T maps to NM_001004476.1 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:78415118 A>T maps to NM_001713.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr5:81354374 C>G maps to NM_031482.4 S57*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr4:2648483 C>T maps to ENST00000324666 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr3:49028270 G>A maps to NM_177938.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr8:19690801 G>A maps to NM_018142.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr13:100635172 A>G maps to NM_007129.2 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chrX:3227795 G>A maps to NM_015419.3 L2816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr6:34804090 G>T maps to NM_017754.3 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr9:133780630 G>A maps to NM_001145106.1 S372S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr1:145439909 T>C maps to NM_006472.3 N152N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6362-01A-11D-1786-08 chr22:19241487 C>T maps to NM_007098.3 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:46493408 A>T maps to NM_015112.2 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:7680785 C>G maps to NM_020877.2 S1694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:67252296 C>T did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:149826609 T>C maps to NM_139126.2 K486K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:65300334 A>C maps to NM_002227.2 Y1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr1:247014375 G>C maps to ENST00000428671 A1682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr2:179537131 A>G did not map to a codon.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr13:43872564 C>A maps to NM_001127615.1 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr6:69758170 C>T maps to NM_001704.2 N734N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr11:85459456 A>T maps to NM_001162953.1 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr17:67513025 C>T maps to NM_002758.3 C38C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6363-01A-21D-1786-08 chr5:145641191 G>A maps to NM_018989.1 W671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr2:54753665 G>A maps to NM_003128.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr11:71259903 C>T maps to ENST00000422553 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr13:21436892 G>T maps to NM_022459.4 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr9:82320808 C>T maps to ENST00000376537 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6364-01A-21D-1786-08 chr4:25678364 C>T maps to NM_006424.2 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr1:167095420 C>T maps to NM_001080426.1 Y351Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr19:43519266 C>A did not map to a codon.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr5:74056730 T>C maps to NM_032380.3 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr1:53728130 G>A maps to NM_004631.3 N587N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:1679917 C>T maps to NM_002615.4 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr16:70818708 G>A maps to NM_018052.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr20:57415469 C>T maps to NM_016592.2 Y103Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr7:44185093 A>G did not map to a codon.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr9:117052372 A>G maps to NM_032888.2 P1414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6365-01A-11D-1786-08 chr17:80726351 T>C maps to NM_005993.4 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr2:152732967 C>A maps to NM_000726.3 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr1:246810984 A>G maps to NM_152609.2 G494G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr17:37881013 T>C maps to NM_004448.2 Y781Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr2:234237162 C>T maps to NM_000541.4 A184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr22:24460517 G>A maps to NM_012295.3 L635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr12:100452767 A>G maps to NM_015054.1 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr19:36275139 G>A maps to ENST00000007510 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr12:102072012 T>A maps to NM_002465.2 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr19:10468471 C>A maps to NM_003331.4 E812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr8:142178472 G>A maps to NM_014957.2 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6366-01A-11D-2114-08 chr1:153314145 G>A maps to NM_020393.2 G194G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G9-6366-01A-11D-2114-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:44153049 T>C maps to NM_133259.3 R929R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6367-01A-11D-1786-08 chr2:203149109 G>T maps to NM_015934.3 E114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr12:51138472 G>T maps to NM_173602.2 E1528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr17:16321002 T>C maps to NM_016113.4 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr13:42742921 A>G maps to NM_178009.2 K445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr8:106813419 C>T maps to NM_012082.3 F370F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr3:101047391 T>C did not map to a codon.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr3:78667055 C>T maps to NM_002941.3 E1337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr6:32053653 C>A maps to ENST00000375244 V1007V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr4:6995921 C>T maps to NM_001113361.1 D285D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr7:33138943 C>T maps to NM_203288.1 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr2:70680365 G>A maps to NM_003236.2 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr9:72131394 G>A maps to NM_001163.3 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chrX:44171918 T>C maps to ENST00000420999 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6369-01A-21D-1961-08 chr2:238243485 G>A maps to NM_004369.3 S3004S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr1:16778445 T>C maps to NM_018090.4 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr9:125860017 A>G did not map to a codon.
Sequencing variant TCGA-G9-6370-01A-11D-1786-08 chr3:190345112 A>G maps to NM_002182.3 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr12:133351741 G>A maps to NM_005895.3 R1376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr3:107885799 A>G maps to ENST00000457963 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr7:139268746 G>A maps to NM_022740.4 S927S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr1:229666036 C>T maps to NM_012089.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr1:237870321 C>T maps to NM_001035.2 I3218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr11:119243941 G>A maps to NM_004205.4 P83P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6371-01A-11D-1786-08 chr7:141752696 C>T maps to ENST00000475668 S1024S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr22:50987890 G>A maps to NM_138433.3 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr3:155206587 G>A maps to ENST00000340059 N788N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr4:175416698 C>A maps to NM_000860.4 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr22:24384212 G>A maps to NM_000853.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr2:36691751 C>T maps to NM_016441.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr1:200878354 C>T maps to NM_018265.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr9:72131721 G>A maps to NM_001163.3 A135A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr12:57574173 C>T maps to NM_002332.2 I1766I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr1:75038905 C>A maps to NM_001002912.4 E830*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr18:3135566 C>A maps to NM_003803.3 V729V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G9-6377-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr8:131848632 G>A maps to NM_001115.2 S855S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chrY:4967493 T>A maps to NM_032973.1 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr2:86067398 G>A maps to NM_003896.3 F375F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr15:48054505 A>G maps to NM_153618.1 K216K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr12:53666574 T>G maps to NM_012291.4 S480S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr3:132165394 G>T did not map to a codon.
Sequencing variant TCGA-G9-6377-01A-11D-1961-08 chr4:20255578 C>A maps to ENST00000273739 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:42839683 C>A maps to NM_153260.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr14:68220895 C>A maps to NM_015346.3 V2340V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr13:35733541 G>A maps to ENST00000400445 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr7:48443342 C>A maps to NM_152701.3 G3979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr17:39388890 C>T maps to NM_031962.2 C46C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr8:8238939 G>C maps to NM_001080826.1 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr11:66026226 G>T maps to NM_022822.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:51676021 G>A maps to NM_181789.2 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr5:90106487 C>T maps to NM_032119.3 F5137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr15:51795001 C>T did not map to a codon.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr6:31940214 C>T maps to NM_032454.1 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chrX:151900632 G>A maps to NM_005367.5 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr5:141017908 C>G maps to NM_173828.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6378-01A-11D-1786-08 chr1:94506836 G>A maps to NM_000350.2 C1150C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr3:142681386 G>A maps to NM_198504.2 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr19:6387479 G>C maps to NM_002096.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr2:47278909 C>T maps to ENST00000394850 A705A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr1:54360026 G>A maps to NM_000792.5 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr19:38959778 C>T maps to NM_000540.2 D1185D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr12:49485160 C>T maps to NM_021044.2 E105E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr12:53777377 C>G maps to NM_138473.2 G549G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr11:118949954 C>A maps to NM_021729.4 R794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6379-01A-11D-A31L-08 chr12:54403268 C>A maps to NM_022658.3 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr5:160033838 C>A maps to NM_025153.2 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr5:99871329 C>T maps to NM_198507.1 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr16:30620888 A>C maps to NM_138447.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr2:12863618 C>T maps to NM_021643.3 D168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr19:375679 C>T maps to NM_016585.3 E97E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr22:28194935 C>T maps to NM_002430.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr1:158299692 G>A maps to NM_001764.2 R186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr16:27585274 G>T maps to NM_015202.2 E21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6384-01A-11D-1786-08 chr8:144643540 C>T maps to NM_024736.6 D228D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr14:58896078 A>G did not map to a codon.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr3:64084857 G>A maps to NM_198859.3 R802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr12:57032139 T>C maps to NM_001686.3 K519K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr9:33056917 C>T maps to NM_018225.2 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr1:228481210 C>T maps to NM_001098623.1 D3675D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr5:150922323 T>C maps to NM_001447.2 G2788G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr19:52793388 G>A maps to NM_001010851.2 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr6:32163813 C>T maps to NM_004557.3 A1804A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr16:47533727 C>T maps to NM_000293.2 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr20:30363691 G>T maps to ENST00000340513 E211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr2:45233548 C>T maps to NM_016932.4 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr20:36974955 C>T maps to NM_004139.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr19:12501648 T>A maps to NM_001080821.2 V521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr12:113822715 C>G maps to NM_173542.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr2:220331956 C>T maps to NM_005876.4 A981A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr10:44104059 A>T did not map to a codon.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr17:38555126 G>T maps to ENST00000357601 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr6:111498552 C>T maps to NM_018593.4 G209G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr1:91781958 C>A maps to NM_001017975.3 E963*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6494-01A-11D-1786-08 chr3:98519474 A>C maps to ENST00000326857 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr7:76029804 G>A maps to NM_080744.1 D91D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr10:70446225 G>A maps to NM_030625.2 K1722K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr5:126771181 G>C did not map to a codon.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr1:99422182 G>A maps to NM_001037317.1 R118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr20:1600529 G>A maps to NM_006065.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr9:131107631 C>G maps to NM_005094.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr7:101845117 C>T maps to ENST00000360264 G858G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr2:211541793 C>T maps to NM_001122633.1 V1452V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6496-01A-11D-1786-08 chr2:166020179 C>T maps to NM_006922.3 A214A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr19:51227211 T>G maps to NM_002975.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr10:48389893 C>G maps to NM_002900.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr19:51451964 A>G maps to NM_012427.4 D219D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr11:4130908 C>T maps to NM_001033.3 F141F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr6:136913364 G>T maps to NM_005923.3 I1057I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr14:70477513 A>G maps to NM_001034852.1 E236E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr5:140176000 G>A maps to NM_018905.2 A484A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6498-01A-12D-A30X-08 chr17:48685231 G>A maps to NM_018896.3 S1519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr19:38056279 C>T maps to NM_016536.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr6:89888604 T>G maps to NM_002042.3 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr11:123813654 C>A maps to NM_001005187.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr17:38638447 A>T maps to NM_032865.5 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr11:94533201 G>T maps to NM_130847.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr16:85936653 A>C maps to NM_002163.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr7:66489942 G>A maps to NM_018264.2 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr21:22782675 G>A maps to NM_004540.2 S426S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr1:155240636 C>T maps to ENST00000368361 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr1:75708579 C>T maps to NM_152697.4 K154K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr12:125397651 T>C maps to NM_021009.5 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6499-01A-12D-1961-08 chr1:226059716 G>A maps to NM_014698.2 S101S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr1:1389855 T>G maps to NM_001039211.2 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr7:30395398 G>A maps to NM_147128.3 Q207Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr6:37280703 G>C maps to NM_017772.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr8:99440614 C>T maps to NM_020697.2 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr12:10163421 C>T maps to NM_001129998.1 R22*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G9-7510-01A-11D-2260-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr8:28574583 G>A maps to NM_001440.2 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr8:143995678 C>T did not map to a codon.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr10:74714238 G>A maps to NM_032562.2 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr2:179456527 A>G maps to NM_133378.4 G17438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr2:165765266 C>A maps to ENST00000409662 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr2:177036308 G>A maps to NM_006898.4 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7510-01A-11D-2260-08 chr22:46685403 G>A maps to NM_017931.2 E396E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr9:21186978 T>C maps to NM_021068.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr8:97269340 T>C maps to NM_015942.3 E112E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr6:64394234 C>T maps to NM_015153.2 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr6:161020596 A>G maps to NM_005577.2 T1074T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr1:158226846 C>T maps to NM_001763.2 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr8:103291367 G>A maps to NM_015902.4 R2024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7519-01A-11D-2260-08 chr19:51582741 G>A maps to NM_022046.4 R160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr7:73112191 C>G maps to ENST00000423497 G291G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr19:964320 G>A maps to NM_005224.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr3:52412684 C>A maps to ENST00000273600 T2422T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr1:13940849 C>T maps to NM_006474.4 I218I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr5:176720971 T>A maps to NM_022455.4 S2201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr12:50498485 G>A maps to NM_005276.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr5:160114976 T>C maps to NM_025153.2 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr11:5322888 G>A maps to NM_033179.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr14:93684960 G>A maps to NM_175748.3 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr19:19356216 C>T maps to NM_004386.2 N1196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7521-01A-11D-2260-08 chr6:27101128 G>A maps to NM_021064.4 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr6:117245848 C>T maps to NM_173560.3 R525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr22:39134910 C>T maps to ENST00000405018 W603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr9:139912648 G>A maps to ENST00000355090 Y688Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7522-01A-11D-2260-08 chr3:128181920 C>G maps to NM_153330.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr4:147561254 C>T maps to NM_004575.2 H175H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr7:45222941 C>T maps to NM_005856.2 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr15:91422744 C>T maps to NM_002569.2 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr3:175042114 G>A did not map to a codon.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr17:16285496 A>G maps to NM_018955.2 E92E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr3:142396939 G>A maps to NM_001172312.1 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr7:99688237 C>T maps to NM_006833.4 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr3:13407499 G>A maps to NM_024923.2 H626H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr11:63581247 G>A maps to NM_138471.1 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr21:28327145 G>A maps to NM_007038.3 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr6:130467206 A>G maps to ENST00000457563 N405N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr2:120078760 G>A maps to NM_001017927.2 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr15:42631921 C>A maps to NM_198141.2 Y633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr10:23287301 G>A maps to NM_173081.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr17:26951277 G>A maps to NM_014680.2 N1575N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr9:95609133 A>G maps to NM_031486.1 F645F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr3:36898224 A>G maps to NM_014831.2 Y952Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr11:6640070 C>T maps to ENST00000453338 Q64Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr1:185267217 A>C maps to NM_006469.4 Y626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr19:14910063 C>A maps to NM_198944.1 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr15:43579552 G>A maps to NM_052955.2 Q264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr6:33384485 G>A maps to NM_001014433.2 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr1:19481548 C>T maps to ENST00000375267 A2107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr7:106513198 T>C maps to NM_002649.2 S701S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr17:56565350 G>A maps to NM_001080439.1 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr12:6471350 C>T maps to NM_001159576.1 A306A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-7525-01A-31D-2260-08 chr5:150029061 A>C maps to NM_001166209.1 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr2:29237324 T>C maps to NM_199280.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr20:2776681 G>A maps to NM_019609.4 I456I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr9:119065087 T>C maps to NM_002581.3 F1002F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr1:32690026 C>T maps to NM_003757.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr17:3445843 G>A maps to ENST00000381913 N205N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr12:132466836 G>T maps to ENST00000333577 P617P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr19:4543618 C>T maps to NM_032108.3 V887V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr21:41719855 G>T maps to NM_001389.3 T317T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr3:119634999 G>A maps to NM_002093.3 R167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr11:92568222 C>T maps to ENST00000298047 D3353D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr4:78815324 C>T maps to NM_020236.3 Y197Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr2:179702243 C>A maps to NM_173648.3 V1234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr1:159683404 G>A maps to NM_000567.2 G195G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr6:146480671 C>T maps to NM_000838.3 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-7775-01A-11D-2114-08 chr7:5780783 A>C maps to NM_207111.2 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr10:13642287 T>C maps to NM_003675.3 N63N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr17:80401692 C>T maps to ENST00000342572 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr3:52529473 C>T maps to NM_015136.2 F15F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr1:10380117 G>A maps to ENST00000377086 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr10:126682485 T>C maps to NM_022802.2 Q823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr3:47103827 G>A maps to NM_014159.6 R2040*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BX-01A-31D-A30X-08 chr10:126682515 G>A maps to NM_022802.2 G813G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr2:241725858 G>A maps to ENST00000373308 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr17:16593776 C>T maps to NM_014695.1 Y21Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr16:19041625 G>A maps to NM_024847.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr3:52383436 G>A did not map to a codon.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr5:54410069 C>T maps to NM_001170402.1 T512T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr2:121746843 C>T maps to NM_005270.4 G1118G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H9-A6BY-01A-11D-A30E-08 chr16:58545389 G>A maps to NM_001130487.1 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr22:39770547 C>T maps to NM_004711.4 I109I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr1:175054614 C>T maps to NM_022093.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chrX:16720990 G>T maps to NM_001144002.1 S12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr8:120575110 C>A maps to NM_006209.3 E855*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr11:118223126 G>A maps to NM_000073.2 K164K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr15:67664645 C>T maps to NM_001031715.2 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr14:72976880 C>T maps to NM_004296.4 R329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr1:12884844 G>A maps to NM_001146344.1 G422G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr5:82940275 C>A maps to NM_001884.3 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr19:47236331 G>T maps to NM_001039877.1 S234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7075-01A-11D-1961-08 chr12:99837458 G>A maps to NM_152788.3 R523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr12:121880537 G>A maps to ENST00000377071 P902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr19:1113560 C>T maps to NM_014963.2 Q740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr11:44080232 C>T maps to NM_001031854.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr1:34102146 C>T maps to ENST00000373381 P1554P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr3:122259685 G>C maps to NM_031458.2 T501T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr15:48707833 A>G maps to NM_000138.4 N2650N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr11:2549249 T>C did not map to a codon.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr1:20991142 G>A maps to NM_020816.2 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr1:185987440 T>C maps to NM_031935.2 N1809N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr17:35945533 G>A maps to NM_007247.4 R126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr6:36270247 T>C did not map to a codon.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr12:70072611 A>G maps to NM_032735.2 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chrX:3228395 G>A maps to NM_015419.3 C2616C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr2:21233705 G>A maps to NM_000384.2 R2012*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr12:13716715 G>A maps to NM_000834.3 T1152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr1:215368302 C>T maps to NM_001017425.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr10:93253265 G>A did not map to a codon.
Sequencing variant TCGA-HC-7077-01A-11D-1961-08 chr2:231155226 A>G maps to NM_007237.4 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr5:140553993 G>T maps to NM_018940.2 A526A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr12:12037451 G>A maps to NM_001987.4 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr3:121828208 A>T maps to NM_175862.3 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr1:155255753 G>T maps to NM_020897.1 G492G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr8:126448346 T>C maps to NM_025195.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr11:76893184 C>T maps to NM_000260.3 D1031D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr19:4538287 C>T maps to NM_052972.2 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr11:33886236 G>A maps to NM_005574.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr11:64622146 C>T maps to NM_006795.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr3:129695839 G>A maps to NM_007117.3 E170E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr19:23543400 C>A maps to NM_003430.2 G794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr15:22945110 G>A maps to NM_014608.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr14:24789052 G>A maps to NM_139247.3 F876F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7078-01A-11D-2114-08 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7079-01A-11D-1961-08 chrX:48650527 T>C maps to NM_002049.3 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr2:198267738 C>T maps to NM_012433.2 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr10:28822944 G>A maps to NM_016628.3 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:51453322 G>A maps to NM_012427.4 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr3:13896274 G>A maps to NM_004625.3 Y108Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr10:124271536 A>G maps to NM_002775.4 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr8:87549806 C>A maps to NM_003909.3 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr14:105421874 G>A maps to NM_138420.2 F137F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr12:675071 C>T maps to ENST00000433832 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr9:138557737 G>A maps to ENST00000277526 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr1:202205106 G>A maps to NM_001017403.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr11:118516356 C>T maps to NM_015157.2 D1135D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr19:49107167 G>A maps to NM_017708.3 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr13:113732743 G>A maps to NM_001112732.1 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7080-01A-11D-1961-08 chr17:39742795 A>C maps to NM_000526.4 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chrX:55651013 T>G maps to NM_198451.3 A290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr7:154875944 G>A maps to NM_024012.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr7:94037157 G>A did not map to a codon.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr19:51217186 C>T maps to ENST00000391814 A220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:39747938 C>T maps to ENST00000361689 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr16:24801363 C>T maps to NM_014494.2 S467S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr6:47200571 C>A maps to NM_014452.3 G633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr1:148594438 A>G maps to NM_001170755.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7081-01A-11D-1961-08 chr17:8731969 G>A maps to NM_001010855.2 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr3:39450136 T>G maps to ENST00000443003 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr1:152975780 G>A maps to NM_005416.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr4:38798748 C>T maps to NM_003263.3 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr20:2842495 G>A maps to NM_022575.2 G315G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr8:145697576 G>A maps to NM_145754.2 E514E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr3:71037203 G>A maps to NM_032682.4 Q363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr10:88447003 C>T maps to NM_001171610.1 Q290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr18:71790684 G>A maps to NM_001142958.1 H352H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7209-01A-11D-2114-08 chr18:21134924 G>T maps to NM_000271.4 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr4:129121698 C>T maps to NM_018078.2 Q730*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr4:90034421 A>G maps to NM_145715.2 G99G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr7:139285233 G>A maps to NM_022740.4 A788A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr7:70252228 C>A maps to NM_015570.2 P781P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr2:27822523 C>T maps to NM_032434.2 Q118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr14:105416336 A>C maps to NM_138420.2 T1817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr3:32571119 T>G maps to NM_016141.3 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr16:314963 C>T maps to NM_032039.2 D534D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr1:101198103 C>T maps to NM_001078.3 N552N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr10:127441483 G>C did not map to a codon.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr5:127710363 A>G maps to NM_001999.3 C684C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr2:235405079 T>A maps to ENST00000339728 K51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr9:123367896 T>C maps to ENST00000426959 E497E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr15:73029879 G>A maps to NM_033028.3 A504A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr10:408504 G>A maps to NM_014974.2 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7210-01A-11D-2114-08 chr1:52941094 C>G maps to NM_001009881.2 T712T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr1:228466408 G>A maps to NM_001098623.1 V2293V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr1:53975546 T>G maps to NM_147193.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr6:85457763 G>A maps to NM_001080508.1 H271H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr14:105420974 C>A maps to NM_138420.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7211-01A-11D-2114-08 chr2:60689482 G>A maps to NM_022893.3 H188H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr7:16640445 G>A maps to NM_020319.2 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr10:12595223 C>T maps to NM_153498.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr17:15971375 G>A maps to ENST00000395857 Q1541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr9:95418827 C>T maps to NM_022755.5 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr13:47469887 G>A maps to NM_000621.3 R52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr17:72926527 T>C maps to NM_178160.2 G266G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr8:41529903 G>A maps to ENST00000415018 T1688T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr7:100031159 C>T maps to NM_019606.5 R685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr17:7806621 C>T maps to NM_001005271.2 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr2:80529774 C>T maps to NM_178839.4 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr12:53819284 A>G maps to NM_020547.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr15:90447060 G>A maps to ENST00000398333 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7212-01A-11D-2114-08 chr14:38679034 T>A maps to NM_001049.2 C147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr18:54547244 C>A maps to NM_015285.2 T1125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr4:123091779 G>A did not map to a codon.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr11:125450014 C>A maps to ENST00000278903 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr8:85097148 A>T did not map to a codon.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr4:100534203 C>T maps to ENST00000511045 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr1:76397715 G>A maps to NM_080868.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr1:39783025 A>G maps to ENST00000361689 K1248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr19:9005697 G>A maps to NM_024690.2 D13236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr5:7414747 G>A maps to NM_020546.2 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr2:228881543 C>T maps to NM_001142644.1 S1342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr7:150174546 C>T maps to NM_175571.2 Y559Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr6:13697084 C>T maps to NM_005493.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr17:7096377 C>T maps to NM_001365.3 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr3:146246433 T>C maps to NM_021105.2 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr10:129899950 G>A maps to NM_002417.4 R3092R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr10:106976776 C>T maps to NM_014978.1 D877D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr15:42679976 C>T maps to NM_000070.2 D175D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr3:146307580 C>T maps to NM_001085420.1 K212K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr17:7578554 C>T did not map to a codon.
Sequencing variant TCGA-HC-7213-01A-11D-2114-08 chr19:8668747 G>A maps to NM_030957.2 D152D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr14:73459967 C>T maps to NM_021260.2 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr10:89692848 G>A maps to NM_000314.4 W111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr5:72195833 A>G maps to NM_002270.3 A780A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr5:179564989 G>A maps to NM_175062.3 T21T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HC-7230-01A-11D-2114-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr1:108023233 G>A maps to NM_001113226.1 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr11:123516293 C>T did not map to a codon.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr21:43967226 A>C maps to NM_018964.3 R249R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr21:27840930 G>A maps to ENST00000435845 H119H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr19:45911966 G>A maps to ENST00000423698 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr2:233546302 C>T maps to NM_025202.3 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr5:140595971 A>G maps to NM_018933.2 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr1:67147852 G>A maps to ENST00000237247 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7230-01A-11D-2114-08 chr2:220116306 G>A maps to NM_006000.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr16:28631395 C>T maps to NM_177536.2 W42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr3:87018022 G>A maps to NM_016206.2 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr11:59559663 C>A maps to NM_004177.4 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr16:2579488 C>T maps to NM_001145815.1 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr7:25264784 G>A maps to NM_022150.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr5:140250250 G>A maps to NM_018902.3 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr3:49313858 C>A did not map to a codon.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr16:12798660 G>A maps to NM_018340.2 Q179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr1:158517226 G>A maps to NM_001005189.1 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr12:77419607 C>T maps to NM_203394.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr20:60884511 G>C maps to NM_005560.3 P3656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr22:36897390 G>A maps to NM_001102371.1 Y371Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chrX:125685919 C>T maps to NM_178470.4 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr6:100841375 G>T maps to ENST00000262901 V519V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr6:34003798 G>A maps to NM_000841.1 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr19:46388639 A>G maps to NM_015649.1 T131T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr7:44259780 G>A maps to NM_001220.4 D627D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr17:10296219 C>T maps to NM_002472.2 Q1797Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr11:76371901 G>A maps to NM_001128922.1 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7231-01A-11D-2114-08 chr3:100964784 C>T maps to NM_016247.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr3:183901337 C>T maps to ENST00000411763 S439S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr11:55761663 G>A maps to NM_003697.1 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr6:128294292 G>A maps to ENST00000368210 G1399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr19:50462137 G>A maps to NM_052884.2 N375N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr20:42635233 G>A maps to ENST00000348077 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr8:42045028 C>A maps to NM_000930.3 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr6:30121515 G>A maps to NM_052828.2 C379C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr10:50953437 G>A maps to NM_018245.2 Y527Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr22:24581634 G>A maps to NM_019601.3 R359R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr14:25101105 C>T maps to ENST00000382542 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr1:185959467 C>T maps to NM_031935.2 S1090S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr15:75798218 G>A maps to NM_002833.2 N255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr15:71185231 T>G did not map to a codon.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr13:100622585 C>T maps to NM_033132.3 E448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chr12:57111704 G>A maps to NM_001113203.1 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7232-01A-11D-2114-08 chrX:154182173 G>A maps to NM_000132.3 I632I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr4:114290837 C>T maps to NM_001148.4 P3829P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr16:53485705 T>C maps to NM_005611.3 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr4:4281392 A>T maps to NM_017816.2 V107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr9:124064267 G>T maps to NM_000177.4 E58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr12:13061953 G>A maps to NM_003979.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr10:98764484 G>A maps to NM_003061.2 Y1225Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr8:113317093 G>A maps to NM_198123.1 R2708*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr2:224849662 C>T maps to NM_001136530.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr5:140475282 G>T maps to NM_018936.2 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr4:6302430 G>A maps to NM_006005.3 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr6:1313421 G>A maps to NM_033260.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr7:48018174 C>A maps to NM_004507.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr19:41007897 C>T maps to NM_020971.2 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chr22:26884137 T>C maps to NM_001013694.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7233-01A-11D-2114-08 chrX:43571168 T>A maps to NM_000240.2 I119I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr10:60994190 T>C maps to NM_032439.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr4:79334178 G>A maps to NM_025074.6 A1455A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr2:74750441 G>T maps to NM_133637.2 R347R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr11:119043648 T>C maps to NM_024618.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr10:73491777 G>A maps to ENST00000398860 S1255S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr15:29346407 C>T maps to NM_005503.3 D107D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chr15:33938649 C>T maps to NM_001036.3 C1288C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7736-01A-11D-2114-08 chrX:54989708 C>T maps to NM_002625.2 W68*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7737-01A-11D-2114-08 chr7:22349654 G>A maps to ENST00000405243 F148F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7737-01A-11D-2114-08 chr2:189599334 A>G maps to NM_052952.2 *105Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7737-01A-11D-2114-08 chr5:140735009 C>T maps to NM_018917.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr16:72991391 G>A maps to NM_006885.3 Q885*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr10:15103732 A>G maps to NM_018324.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr5:45645595 C>T maps to NM_021072.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr4:110972796 C>T maps to NM_024090.2 W165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr20:32248141 C>A maps to NM_031232.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr5:35876449 G>C maps to NM_002185.2 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr4:54440052 G>A maps to NM_001126328.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr3:120365111 A>G did not map to a codon.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr8:144998993 C>T maps to NM_201380.2 A1838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr4:86916228 G>A maps to NM_001025616.2 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr19:12155152 G>T maps to NM_001080404.1 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr1:147380381 C>T maps to NM_005267.4 V100V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr3:69168011 C>A maps to NM_198271.3 R498R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr1:24419566 C>T maps to ENST00000330966 K321K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr8:38157096 G>A maps to NM_023034.1 Q875*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr5:3600021 G>C maps to NM_024337.3 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr20:39832182 G>A maps to NM_015035.3 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr19:38934380 C>T maps to NM_000540.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr11:18313151 T>C maps to NM_181507.1 G759G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr10:50835781 G>A maps to NM_020549.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr7:31862843 C>T maps to NM_001191057.1 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7740-01A-11D-2114-08 chr12:73056935 C>T maps to NM_013381.2 D1012D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr22:50893709 G>A maps to ENST00000337034 A1509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr5:41159223 G>A maps to NM_001115131.1 R606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr19:45579625 G>A maps to NM_145288.1 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr13:45148695 T>C maps to NM_183422.2 Q505Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr1:237982394 C>T maps to NM_001035.2 I4831I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr19:3762706 C>G maps to NM_172251.2 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr3:125824674 G>A maps to ENST00000273450 V859V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr6:100390895 C>T maps to NM_032503.2 S172S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr17:40717504 G>T maps to NM_001042532.2 V497V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7742-01A-11D-2114-08 chr7:48352728 C>T maps to NM_152701.3 S3194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr12:69986784 T>C maps to NM_006431.2 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr2:32312618 A>G maps to NM_014946.3 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr12:26277808 G>A did not map to a codon.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr6:69349085 T>G maps to NM_001704.2 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr16:89831296 C>T did not map to a codon.
Sequencing variant TCGA-HC-7744-01A-11D-2114-08 chr1:235338685 T>G maps to NM_016374.5 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr11:77924825 C>T maps to NM_020798.2 G1008G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr11:61574166 C>T maps to NM_013402.4 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr4:82064094 G>A maps to NM_006259.1 S420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr3:66428191 G>A maps to NM_173471.3 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr11:32610272 G>A maps to NM_006360.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr11:47296302 G>A maps to NM_003682.3 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr14:20711207 C>T maps to NM_001004479.1 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr4:141317053 A>G maps to NM_004362.2 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr1:231471574 C>T maps to NM_175876.3 L639L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr17:56585535 G>A maps to NM_004687.4 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr5:43700277 T>G maps to NM_182977.2 A978A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr21:37617883 C>T maps to NM_005128.2 L1202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr19:40580581 C>T maps to NM_001142577.1 E590E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr11:122774731 G>A maps to NM_024806.2 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr5:94022424 T>G did not map to a codon.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr1:152282807 A>G maps to NM_002016.1 H1518H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr15:90293434 A>C maps to NM_018670.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr1:12887685 T>C maps to NM_001146344.1 R57R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr7:1024634 G>A maps to NM_017781.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7745-01A-11D-2114-08 chr9:107379675 T>C maps to NM_001001956.1 S270S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:43026109 C>T maps to NM_001712.4 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:38858383 C>T maps to NM_021185.4 D966D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr6:3287258 C>A maps to ENST00000436008 P460P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr3:38139332 G>A maps to NM_007335.2 Q888Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr5:33947261 G>A maps to NM_001012509.2 C458C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr5:80548570 C>T maps to NM_001825.2 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:16060515 C>T maps to NM_001004465.1 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:1615476 C>T maps to NM_003200.2 K543K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr15:81427610 G>T maps to ENST00000458088 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr3:38743402 G>A maps to NM_006514.2 F1528F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr12:118298122 G>A maps to ENST00000339824 I98I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr18:19153549 G>A maps to NM_052911.2 R419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr2:170136032 G>A maps to NM_004525.2 L472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr11:74904263 C>A maps to NM_007256.4 V359V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr1:65142589 C>T maps to ENST00000371073 C996C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr6:132645228 T>G maps to NM_015529.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:40730406 G>A maps to NM_024877.3 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr17:38567941 T>C maps to ENST00000357601 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr2:74750267 C>T maps to NM_133637.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr6:36931338 C>T maps to NM_153370.2 T407T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr2:109365451 C>T maps to NM_006267.4 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr16:57088674 G>A maps to NM_032206.3 T1173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr15:42147469 C>T maps to ENST00000320955 A3125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr16:22926768 A>G maps to NM_006043.1 K330K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr4:74010531 A>C maps to NM_032217.3 G629G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr8:132966121 T>C maps to NM_015137.3 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7747-01A-11D-2114-08 chr19:12575379 C>T maps to ENST00000428311 Q452Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr2:206641225 G>A maps to NM_018534.3 E899E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr15:101425524 A>C maps to NM_000693.2 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr2:170493057 A>G maps to NM_004792.2 K430K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr6:131216166 C>T maps to NM_001431.3 P443P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr4:47938767 G>C maps to NM_001142564.1 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr4:62903459 G>A maps to ENST00000506720 E1201E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7748-01A-11D-2114-08 chr8:10468679 C>T maps to NM_178857.5 A976A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr16:49669906 C>T maps to NM_015069.2 A1052A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr13:84454930 G>A maps to NM_052910.1 R238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr6:30459139 G>C maps to NM_005516.5 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr18:22008831 G>A did not map to a codon.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr8:2806883 C>A maps to NM_033225.5 G3447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr10:102849596 G>A maps to NM_001085398.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr11:102710882 A>G maps to NM_002422.3 D297D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr5:145834700 C>T maps to NM_006706.3 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr19:59059686 C>G maps to NM_005762.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr14:21109304 G>A maps to NM_001001968.1 C182C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr17:78857259 C>T maps to NM_020761.2 I542I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr13:101833450 G>A maps to ENST00000376196 R668*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr6:87969689 C>T maps to NM_015021.1 R2115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr19:12978319 C>T maps to NM_014975.2 H724H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr1:9099649 G>A maps to NM_003039.2 A319A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr5:54281324 C>G maps to NM_007036.4 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr14:92548748 C>A maps to ENST00000359819 E224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr9:100447234 T>A maps to NM_000380.3 K215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr11:94230130 T>A did not map to a codon.
Sequencing variant TCGA-HC-7749-01A-11D-2114-08 chr21:27945367 G>A did not map to a codon.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr17:41957293 G>A maps to NM_005374.3 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr19:40903196 G>A maps to NM_181882.2 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr9:103055172 T>C maps to NM_014425.2 D878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr20:30729617 C>A maps to NM_014742.3 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chrX:102931634 G>A maps to NM_001142432.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr19:57301239 C>T maps to NM_001146326.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr11:11969589 C>A maps to ENST00000399455 R1071R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr11:63764356 G>T maps to ENST00000422031 E160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr1:22924680 C>T maps to NM_020526.3 N718N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr10:46248087 G>A maps to ENST00000399588 S352S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr21:44427674 T>C maps to NM_004571.3 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr17:80121089 G>A maps to ENST00000445854 R676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chrX:138678881 G>A maps to ENST00000370578 S846S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr1:153520901 T>G maps to NM_002960.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr2:170493493 C>T maps to NM_004792.2 R576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr10:26575311 C>G maps to NM_001134366.1 Y425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr3:179320487 C>A maps to NM_020409.2 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr10:24669919 T>C maps to NM_019590.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chrY:4968732 C>T maps to NM_032973.1 S1038S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr15:43654115 C>A maps to NM_152455.3 E572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chrX:153187218 C>A maps to NM_001164741.1 L37L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr13:20067610 G>A maps to NM_199254.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7752-01A-11D-2114-08 chr16:2011660 C>T did not map to a codon.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr11:46801809 A>C maps to ENST00000415402 S789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr8:26366212 G>T maps to NM_007257.5 S20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr1:229738250 G>A maps to NM_014409.3 N221N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr2:63101582 G>A maps to NM_015252.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr5:90083964 C>T maps to NM_032119.3 S4577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr21:28327085 G>A maps to NM_007038.3 H403H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr14:24793575 C>T maps to NM_139247.3 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr17:45668126 G>A maps to NM_006310.3 W380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr22:21354949 T>C maps to NM_030573.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr1:111061226 C>T maps to NM_005549.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7817-01B-11D-A29Q-08 chr6:43623375 C>T maps to NM_152732.4 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr11:20409623 G>T maps to NM_005788.3 E30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr10:26559615 C>T maps to NM_001134366.1 Y341Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr22:42981904 G>A maps to ENST00000415122 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr1:17548934 C>A maps to NM_013358.2 G81G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr1:248309106 C>T maps to NM_001004690.1 R220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr8:124267244 A>G maps to NM_007222.3 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr1:181708365 C>A maps to ENST00000357570 G1232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr11:117332279 G>A maps to NM_020693.2 L1160L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr17:10442557 G>T maps to NM_017534.5 I460I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr10:98806791 C>T maps to NM_003061.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7818-01A-11D-2114-08 chr12:54757586 G>A maps to NM_020370.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr3:100368588 C>T maps to NM_032787.2 N439N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr21:45379681 G>A maps to NM_001037553.1 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr13:99354750 T>C maps to NM_005073.3 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr21:46233854 C>T maps to ENST00000411651 V62V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr10:88718534 G>A maps to NM_003087.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr5:150922047 G>A maps to NM_001447.2 H2880H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr16:2233834 G>A maps to NM_020764.3 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr11:101775572 A>G maps to NM_178127.4 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr19:31770233 G>A maps to NM_020856.2 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr10:124214266 G>T maps to NM_001099667.1 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr15:75982727 T>C maps to NM_001897.4 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7819-01A-11D-2114-08 chr22:50659211 A>G maps to NM_020461.3 S1192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr3:49004608 C>T maps to NM_006321.2 R147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr19:38655513 G>A maps to NM_015073.1 A1392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr6:123127402 G>A maps to NM_006714.3 V315V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr18:24128245 C>T maps to NM_001142730.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr4:109740458 T>C maps to ENST00000333642 K624K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr4:69198539 T>C maps to NM_001031732.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr3:167000275 T>C maps to ENST00000307529 K668K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr4:15835905 G>A maps to NM_001775.2 W189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr19:56466878 C>T maps to NM_176811.2 T485T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr18:56246186 C>T maps to NM_052947.3 Q607Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr17:39502451 A>G maps to NM_004138.2 C378C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr12:132547140 G>A maps to ENST00000333577 Q2779Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr17:38906789 C>T maps to NM_181534.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr1:147084928 C>T maps to NM_004326.2 R101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr1:207930435 C>A maps to NM_172359.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr7:98254300 C>T maps to NM_002523.2 Y237Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr20:56726067 T>G maps to NM_178456.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr1:150471025 A>G maps to NM_025150.3 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr5:40958241 T>C maps to NM_000587.2 H456H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr22:50716551 T>C maps to NM_012401.2 S1627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr13:32911290 A>T maps to NM_000059.3 T933T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7821-01A-12D-2114-08 chr16:23555839 C>G maps to NM_001083614.1 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr9:2039778 G>A maps to NM_003070.3 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr13:76379698 G>A maps to ENST00000357063 E263E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr3:62535599 C>G maps to ENST00000383709 L648L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr1:196711059 G>A maps to NM_000186.3 K1004K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr16:78466399 C>T maps to NM_016373.1 N269N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8213-01A-11D-A29Q-08 chr15:85164526 C>T maps to NM_181877.3 C367C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr12:52820635 C>A did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr19:50461936 C>A maps to NM_052884.2 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:248525214 C>T maps to NM_001004696.1 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr22:21349316 T>G did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:209879154 G>C did not map to a codon.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr6:117662660 G>A maps to NM_002944.2 L1602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:89444999 C>A maps to NM_005233.5 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr5:427995 G>A maps to NM_020731.3 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:128262665 G>C maps to NM_017969.2 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr18:39607409 T>C maps to ENST00000398870 Y497Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:151137674 C>T maps to NM_212551.4 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:38592950 G>T maps to NM_001099404.1 R1638R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr5:137803631 G>A maps to NM_001964.2 T498T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr10:75029380 G>A maps to NM_145170.3 V1076V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:50885065 C>T maps to NM_032110.1 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr6:85446702 G>A maps to NM_001080508.1 F508F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:220350131 A>G maps to NM_005876.4 L2558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:182587058 C>T maps to NM_014616.1 L602L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr20:30897747 C>G maps to NM_004798.3 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr10:103649192 G>A maps to NM_024541.2 H612H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr1:160850468 C>T maps to NM_017625.2 K198K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr15:33988495 C>T maps to NM_001036.3 R1980*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr20:57576622 G>A maps to NM_001336.3 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr19:11233931 A>T maps to NM_000527.4 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr9:77390916 G>T maps to NM_017662.4 Y1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr8:134488180 G>C maps to NM_173344.2 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr10:72511283 C>T maps to NM_139155.2 Y829Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr11:16071442 G>T maps to NM_001145819.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr9:107361056 A>T maps to NM_001004482.1 L213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr5:169507216 G>A maps to NM_004946.2 A1739A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:45773896 A>G maps to NM_018079.4 Y616Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr15:40313179 A>G maps to NM_001013703.2 K1418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:182586926 C>T maps to NM_014616.1 Q584*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr6:90661074 G>A maps to NM_001170794.1 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr19:9086743 T>A maps to NM_024690.2 R1691*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr12:108603945 C>T maps to ENST00000261400 G182G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:62570915 A>G maps to ENST00000383709 D507D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr3:108754262 G>A maps to NM_014429.3 I461I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr20:61596499 G>C maps to NM_022082.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr2:3691605 C>T maps to ENST00000418971 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr17:38062396 G>A maps to NM_001165958.1 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr5:89933654 T>C maps to NM_032119.3 F710F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8216-01A-11D-A29Q-08 chr20:17410082 C>T maps to NM_002594.2 H208H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr3:175041962 G>T did not map to a codon.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr16:2770146 C>T maps to NM_031948.3 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr8:24254908 G>A maps to NM_014479.3 V189V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr19:35613745 G>T maps to NM_021910.2 E59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr6:33168112 C>T maps to ENST00000374685 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr1:180793907 A>T maps to NM_004736.3 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr4:144826670 C>T did not map to a codon.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr17:34934520 G>A maps to NM_024835.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr17:3379479 A>G maps to NM_000049.2 E9E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr7:106508995 G>T maps to NM_002649.2 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr19:15582852 C>T maps to NM_052890.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr22:46835237 G>A maps to NM_014246.1 C1418C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr21:33318387 G>A maps to NM_014586.1 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr1:16577178 G>A maps to NM_018994.1 R714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr17:10404783 C>T maps to NM_005963.3 E1127E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr20:18142698 A>G maps to NM_020536.4 K306K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr20:9546932 T>C maps to NM_177990.2 K363K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chrX:118783980 G>A maps to ENST00000394612 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr16:67159902 C>T maps to NM_025187.3 D63D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr11:19077805 G>A maps to NM_054030.2 N48N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr19:43411266 G>A maps to NM_002782.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr17:3649105 G>A maps to NM_002208.4 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr20:49626293 G>A maps to NM_002237.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr4:89671666 G>C maps to NM_014883.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr16:68104842 C>T maps to NM_017803.3 N214N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr1:228452054 C>T maps to NM_001098623.1 A1608A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr1:198719700 C>T maps to ENST00000271610 F1051F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr15:25221556 C>A maps to NM_022805.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr9:114468872 C>A maps to NM_173521.3 V840V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr2:111562875 G>A maps to NM_001142807.1 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr11:72420925 G>A maps to NM_001040118.2 Y504Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr20:16409610 C>T maps to NM_024704.4 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr6:16328223 G>A maps to NM_000332.3 Y106Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr3:51992214 G>A maps to NM_033010.2 I358I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr6:17608510 C>T maps to NM_016255.2 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr10:73553230 C>T maps to ENST00000398860 S2187S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr19:49207085 C>T maps to NM_001097638.2 F291F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr1:248616337 C>T maps to NM_001004136.1 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr1:249118996 G>T maps to NM_030645.1 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8257-01A-11D-2260-08 chr6:30520935 G>T maps to NM_005275.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8258-01A-11D-2260-08 chr6:32083516 C>T maps to NM_004381.4 *704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8258-01A-11D-2260-08 chr11:115047193 C>A maps to NM_014333.3 *443Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr1:159163348 C>T maps to NM_021189.3 H207H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr11:113853982 G>T maps to NM_213621.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr11:96117581 T>C maps to NM_024725.3 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr5:37379472 G>T maps to NM_018034.2 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr16:17294397 G>A maps to NM_022166.3 Q343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr10:99667830 C>A maps to NM_018058.4 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr3:33216453 G>A maps to NM_015551.1 G174G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr8:69046378 G>A maps to NM_024870.2 A1284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr1:161967993 G>A maps to ENST00000451379 N366N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr18:72223613 C>T maps to NM_032649.5 R22R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr16:76573709 C>T maps to NM_033401.3 H1104H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr18:54291517 C>A did not map to a codon.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr9:103092360 C>T maps to NM_017746.3 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr6:157527452 C>T maps to ENST00000367148 D1766D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr18:61570298 A>T maps to NM_001143818.1 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr14:89307827 A>G maps to NM_144596.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr4:72623866 T>C maps to ENST00000504199 Q260Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr11:9072167 G>A maps to ENST00000457346 R542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr2:27535938 C>T maps to ENST00000405983 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr2:73518809 G>A maps to NM_001965.3 C515C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr2:190554475 T>G maps to NM_144708.3 Y275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr3:124132348 C>T maps to NM_001024660.3 D791D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8259-01A-11D-2260-08 chr20:3843001 T>C maps to NM_020746.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8260-01A-11D-2260-08 chr10:15255015 G>A maps to NM_001010924.1 H857H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8260-01A-11D-2260-08 chr17:42390844 G>A maps to NM_001144825.1 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8260-01A-11D-2260-08 chr10:82034333 G>A maps to NM_000429.2 R343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8260-01A-11D-2260-08 chr2:163005634 G>A maps to ENST00000233604 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chrX:62857908 C>T maps to NM_015185.2 *517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr14:21860704 T>A maps to NM_001170629.1 R2244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr15:50790906 T>C maps to NM_005154.3 Y1051Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chrX:71351090 C>T maps to NM_001024455.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr4:77677869 C>T maps to NM_020859.3 Q1660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr19:51480875 G>A maps to NM_005046.2 C226C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr14:93399079 C>T maps to NM_001275.3 R392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr2:219507892 C>A maps to NM_001105537.1 E1116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr14:105618059 G>A maps to NM_002226.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr12:56628744 T>A maps to NM_001135195.1 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr9:96320950 C>T maps to ENST00000333936 C947C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr16:22260090 C>T maps to NM_013302.3 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr2:106497793 G>A maps to NM_001004720.2 K79K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr1:17690078 C>T maps to NM_012387.2 N607N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr12:121434122 C>T maps to NM_000545.5 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8261-01A-11D-2260-08 chr6:110944513 A>T maps to NM_015076.3 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr2:11750978 C>T maps to NM_014668.3 C944C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr18:74592172 C>A maps to NM_007345.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr22:25627720 C>T maps to NM_000496.2 A200A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr8:17611560 G>A maps to NM_001001924.2 Q586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr10:88702335 G>A maps to NM_024756.2 N735N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr11:6650984 C>T maps to NM_003737.2 Q1651Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr9:135517390 C>A maps to NM_022779.7 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr2:128050245 G>A maps to NM_000122.1 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr3:48628921 G>A maps to NM_000094.3 Y537Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr2:7160685 G>A maps to NM_014746.3 Q128Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr9:99581088 T>A maps to NM_001001662.1 K406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr9:130438177 T>C maps to NM_003165.3 Y402Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr11:77734211 C>A maps to NM_023930.3 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr5:14711383 C>T maps to NM_054027.4 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr17:3979977 C>A maps to NM_015113.3 E1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr11:56258762 C>T maps to NM_001005282.1 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8262-01A-11D-2260-08 chrX:151869831 C>T maps to NM_005363.2 H174H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr5:74325283 C>T maps to NM_016591.2 E193E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr4:39230259 G>T maps to NM_025132.3 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr11:46772925 T>C maps to ENST00000415402 L1764L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr18:21501018 G>T did not map to a codon.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr1:120438878 G>A maps to NM_021794.2 G27G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr17:26818587 G>A maps to NM_001145975.1 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr11:117241959 T>C maps to NM_014956.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chrX:153222852 G>A maps to ENST00000369984 S755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr21:35237514 C>T maps to NM_003024.2 D1317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr1:245850130 G>A maps to NM_018012.3 L1282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8264-01B-11D-2395-08 chr2:160035656 C>G maps to NM_033394.2 A831A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr17:37627876 C>T maps to NM_016507.2 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr16:85111073 G>A maps to NM_014732.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr5:179565028 G>A maps to NM_175062.3 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr6:29142062 T>A maps to NM_030905.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr3:159710860 A>G maps to NM_000882.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr19:40411865 C>T maps to NM_003890.2 A1254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr20:42265849 G>A maps to NM_016004.2 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr14:75264384 C>T maps to NM_019589.2 P795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr17:80282490 T>A maps to NM_003004.2 R124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr9:20414336 G>A maps to NM_004529.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr3:193332787 C>T maps to NM_130837.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr19:19338462 T>C maps to NM_004386.2 Y678Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr12:2764405 T>G did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr2:211336686 C>T maps to NM_001136575.1 W65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr8:22105703 A>G maps to NM_001722.2 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr7:141765239 A>G maps to ENST00000475668 A1530A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr7:82545751 C>T maps to NM_033026.5 Q3850Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr14:64532244 C>G maps to NM_182914.2 G3436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr8:75276268 C>T maps to NM_018972.2 D248D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr15:45003695 A>T did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr11:48346689 C>A maps to NM_001004702.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr10:79571785 C>T maps to NM_004747.3 T1406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr2:179397721 A>T maps to NM_133378.4 Y31972*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr14:52957170 T>C did not map to a codon.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr4:23815647 G>A maps to NM_013261.3 D486D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr9:75445551 T>G maps to NM_138691.2 A738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr19:58213659 A>G maps to NM_001085384.1 C219C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr7:17885262 G>A maps to ENST00000417048 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr12:57674221 C>T maps to ENST00000438036 Q439Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8265-01A-11D-2260-08 chr19:35786681 G>A maps to NM_002361.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr1:153788812 G>C maps to NM_020699.2 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr10:26462762 A>G maps to NM_017433.4 K1190K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr4:25667861 G>A maps to NM_006424.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr2:160289577 A>G maps to NM_013450.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr8:87470209 C>T maps to NM_007013.3 R819*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr8:28206325 C>T maps to NM_018660.2 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr4:42072552 G>A maps to NM_006345.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr1:247588839 C>T maps to NM_004895.4 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr4:84026087 G>A maps to NM_001130715.1 V68V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr2:219249917 C>A maps to NM_000578.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr11:118889680 G>A did not map to a codon.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr11:1780797 G>A maps to NM_001909.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr11:65375264 G>A maps to NM_002419.3 H364H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8266-01A-11D-2260-08 chr9:136260869 C>G maps to NM_153710.3 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr5:121188191 C>T maps to NM_177478.1 H178H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr5:32089964 A>G maps to NM_178140.2 A2137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr6:146264542 G>A maps to ENST00000367503 R658R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr7:143792958 C>T maps to NM_001004135.1 S253S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr19:50214113 G>A maps to NM_152359.2 T622T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr22:36123053 C>T maps to NM_030642.1 S313S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr20:35261965 G>A maps to NM_032214.2 H86H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr15:85403129 T>G maps to NM_020778.4 P1565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A48F-01A-11D-A257-08 chr8:30436472 G>A maps to NM_002095.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr18:12699202 C>A did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:169483631 G>A maps to ENST00000367796 S2203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr22:28193261 G>A maps to NM_002430.2 G1090G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr17:48741194 G>T maps to NM_003786.3 G384G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr12:21392116 T>C maps to NM_006446.4 H690H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr10:123842617 G>A maps to NM_206862.2 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chrX:134990667 A>C maps to NM_018666.2 R445R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr5:141694232 C>T maps to NM_030964.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:101487276 T>C maps to NM_015958.2 E60E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr17:29761109 C>T maps to NM_032932.3 C102C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr2:47256511 T>A maps to ENST00000394850 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr3:9855029 G>A did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:51628470 T>G maps to NM_014441.2 A80A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr3:142204016 A>T maps to NM_001184.3 G2062G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr6:132910498 C>T maps to NM_003967.2 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr8:101612610 A>T maps to NM_152628.3 L247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:156877419 C>T maps to NM_001080471.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr5:140773099 G>A maps to NM_032088.1 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:237756846 T>C maps to NM_001035.2 D1449D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:39877440 G>T maps to NM_015038.1 E502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:57065051 G>C did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr11:94039856 G>A maps to NM_001080486.1 W106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:39325294 C>T maps to NM_022157.2 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr21:31709999 C>A did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr13:38213400 T>C maps to NM_003306.1 Q710Q. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HC-A4ZV-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:49858557 A>G did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr21:41301035 G>C maps to NM_006198.2 *63Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr1:59147848 A>T maps to NM_001085487.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr17:58525051 G>A maps to NM_006380.2 Q550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:8670019 C>A maps to NM_030957.2 V104V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:47773662 G>A did not map to a codon.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr11:92086236 G>A maps to ENST00000298047 W320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr17:48614288 C>T maps to NM_017957.2 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr5:120022391 T>C maps to NM_016644.1 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr20:3128063 C>T maps to NM_021826.4 K551K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr19:14887553 G>C maps to NM_013447.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A4ZV-01A-11D-A26M-08 chr20:62384050 C>T maps to NM_025224.2 K462K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr1:24124220 G>A maps to NM_001008216.1 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr12:108604002 C>T maps to ENST00000261400 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr1:19632607 C>T maps to NM_003689.2 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr9:118950480 C>T maps to NM_002581.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr2:174777795 A>G did not map to a codon.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr6:123600200 G>A maps to NM_006073.2 Q513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr13:108881586 G>A maps to NM_032859.2 L7L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr9:17791306 C>T maps to NM_003026.2 Q235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr3:147128792 C>T maps to NM_003412.3 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr1:74575076 C>A did not map to a codon.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr10:73468897 C>T maps to ENST00000398860 A1055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr2:166908357 G>A maps to NM_001165963.1 Q279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr3:129251240 C>T maps to NM_000539.3 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr13:25021263 G>A maps to NM_006437.3 Q1059*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr18:12463457 G>T maps to NM_001128626.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr1:210522366 C>T maps to NM_001170580.1 G16G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chrX:149895774 C>T maps to NM_003828.2 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr4:138452261 T>C maps to NM_019035.3 Q327Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr11:128781512 G>T maps to NM_000890.3 R115R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr5:159680552 G>A maps to NM_024565.5 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A631-01A-11D-A29Q-08 chr5:82815918 G>A maps to NM_004385.4 E598E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr20:62730103 C>T maps to NM_000913.3 D355D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr6:10529593 T>A maps to NM_145649.4 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr1:19403306 G>T maps to ENST00000375267 A5159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr5:55094307 G>A maps to NM_024415.2 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chrX:2726250 C>T maps to NM_001141919.1 G148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr11:65414868 C>T maps to NM_153253.29 G682G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr2:241827876 G>A maps to NM_001085437.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr12:62777655 A>G maps to ENST00000280377 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr1:109801498 C>T maps to NM_001408.2 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr1:196658724 G>A maps to NM_000186.3 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr5:140553172 G>T maps to NM_018940.2 E253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A632-01A-11D-A29Q-08 chr4:140393994 T>C maps to NM_031296.1 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr5:140209184 G>A maps to NM_018909.2 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr7:38807199 T>C did not map to a codon.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr2:167279861 G>T maps to NM_002976.2 I978I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr12:48741843 C>T maps to NM_152320.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr11:55433370 G>T maps to NM_001004704.1 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr9:95403026 G>A maps to NM_022755.5 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr22:39826028 G>A maps to NM_006116.2 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr13:28919629 C>T maps to NM_002019.4 A769A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr14:65194558 C>T maps to ENST00000394691 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr17:3324769 T>C maps to NM_012373.2 N303N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr1:236399659 G>A maps to NM_019891.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr12:133683236 A>C maps to NM_003440.2 *458C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr11:68480779 G>T maps to NM_004923.3 C372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr7:72400573 T>G maps to ENST00000434423 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr19:14774335 G>A maps to NM_032571.3 C31C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AL-01A-11D-A30E-08 chr4:126336324 T>C maps to NM_024582.4 V2069V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr7:77764434 C>A maps to NM_012301.3 V978V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr1:12052705 G>A maps to NM_014874.3 E90E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr7:157931052 C>T maps to NM_002847.3 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr16:23578314 T>C maps to ENST00000219638 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr7:939747 C>G maps to NM_006869.2 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr3:42704606 G>A maps to NM_145166.3 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr11:124252654 G>A maps to NM_001005468.1 N195N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr2:234178653 G>A maps to ENST00000392018 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr1:111216383 G>A maps to NM_002232.3 R350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AN-01A-11D-A30E-08 chr2:223499163 C>T maps to NM_005687.3 K184K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr1:32050622 C>T maps to NM_022164.2 F281F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr7:48428730 T>A maps to NM_152701.3 A3856A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr20:36952274 G>T maps to NM_001725.2 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr5:140187068 C>T maps to NM_018907.2 S99S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr6:52148177 T>C maps to ENST00000419835 K80K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr19:30935518 C>T maps to NM_014717.1 C350C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr12:122441612 C>T maps to NM_144668.4 F1131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr7:48428692 C>T maps to NM_152701.3 L3844L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr3:142499732 A>C maps to ENST00000476941 A274A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr19:6734269 G>A maps to NM_001080452.1 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chrX:151092294 A>G maps to ENST00000427663 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr22:50682159 C>A maps to NM_020461.3 G243G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr15:90320475 G>A maps to NM_001039958.1 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr4:155298458 G>T maps to NM_017639.3 I124I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr15:60919519 C>T maps to NM_134260.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr12:56335368 G>A did not map to a codon.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr11:134240924 C>T maps to NM_138342.3 I413I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr11:64416296 G>T maps to NM_015080.3 G1064G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr7:114269972 A>G maps to NM_148898.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr8:113256713 G>A maps to NM_198123.1 T3437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr15:101592009 C>G maps to NM_024652.3 P1178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr17:73836862 C>T maps to ENST00000412096 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AO-01A-11D-A30E-08 chr11:44069762 G>A maps to NM_001031854.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr6:123319140 G>A maps to NM_001010852.2 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr11:89165956 T>G maps to NM_016931.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr16:72057374 C>T maps to NM_001361.3 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr5:150422162 G>A maps to NM_006058.3 Q358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr15:64047507 G>C maps to ENST00000261887 S517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AP-01A-11D-A30E-08 chr19:38964030 C>T maps to NM_000540.2 D1260D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr17:12032508 T>C maps to ENST00000415385 D326D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr2:132237643 G>A maps to NM_080386.2 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr3:127646681 T>C maps to NM_207335.2 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr13:53419057 C>T maps to NM_002590.2 A950A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr6:26509215 C>T maps to NM_001732.2 S465S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr12:101766715 T>C maps to NM_014503.2 L2285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr8:99441253 C>T maps to NM_020697.2 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr22:50615614 G>T maps to NM_052839.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr20:44575999 C>T maps to NM_022104.3 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr1:102269967 G>A maps to ENST00000338858 S421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr4:16590332 A>G maps to NM_001290.3 H177H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr11:68822729 C>A maps to NM_139075.3 Y113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr1:26449049 T>C maps to NM_152835.3 D336D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr6:26285589 T>G maps to NM_003543.3 R46R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr11:6262660 G>A maps to NM_001037329.2 W306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr6:24564489 G>A maps to NM_014809.3 R791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr19:55831945 A>G maps to NM_001085488.1 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr19:24310304 A>G maps to NM_203282.2 Q501Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr4:71346946 A>G maps to NM_152291.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr10:31809235 C>T maps to NM_001174096.1 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6AS-01A-11D-A30E-08 chr7:137569738 A>G maps to ENST00000456390 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr16:12875120 T>C maps to NM_018340.2 Q70Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr4:170482701 C>A maps to ENST00000507142 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr3:12632412 T>G maps to ENST00000415519 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr3:73450102 C>T maps to NM_015009.1 Q408Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr12:48920025 C>T maps to NM_001005203.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr15:43621412 G>A maps to NM_014793.4 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HX-01A-11D-A31L-08 chr17:37618972 A>T maps to NM_016507.2 K217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr11:10800224 G>C did not map to a codon.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr11:5462693 T>A maps to NM_001005288.2 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr2:8940604 G>A maps to NM_020738.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chrX:135487898 T>C maps to NM_153834.3 Y2901Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr11:111228346 C>T maps to NM_006235.2 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr22:42611325 C>T did not map to a codon.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr1:70504093 C>T maps to NM_020794.2 Q825*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr10:73767310 C>T maps to NM_004273.4 F174F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr11:36615226 A>G maps to NM_000536.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr11:58190359 G>T maps to NM_001005566.2 C125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr19:19309476 G>A maps to NM_003721.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-A6HY-01A-11D-A31L-08 chr1:90048353 C>T maps to NM_015350.2 Q49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr19:49633699 C>T maps to NM_003660.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr3:189349246 A>T did not map to a codon.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr2:100055180 C>T maps to NM_016316.2 K365K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr16:1556316 C>T maps to NM_016111.3 Q705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr17:67300890 G>C maps to ENST00000392677 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr4:26491053 G>A maps to NM_000730.2 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr16:23364120 G>T did not map to a codon.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr13:39433449 C>T maps to NM_207361.4 Y2414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr16:335184 G>A maps to NM_006849.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr5:180048620 G>A maps to NM_182925.4 H647H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr18:6896511 G>T maps to ENST00000400091 P639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr17:39261948 T>C maps to NM_001146041.1 T103T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr1:158639552 T>C maps to NM_003126.2 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr4:81123530 C>A maps to NM_001099403.1 I305I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr18:3102499 G>A maps to NM_003803.3 R1183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr19:49207193 G>T maps to NM_001097638.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr10:15255870 G>A maps to NM_001010924.1 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr11:130079558 T>G maps to NM_021978.3 G803G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr2:10929047 A>T maps to ENST00000381611 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr6:32036413 C>T maps to ENST00000375244 G1991G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr17:42455140 G>T maps to NM_000419.3 I704I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr16:3021852 C>T maps to NM_152341.3 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr6:157150549 C>T maps to ENST00000367148 Q578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr10:38343825 T>C maps to NM_006954.1 D258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr7:22985645 A>G maps to NM_032581.3 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7168-01A-11D-2114-08 chr4:103720583 G>T maps to NM_181890.1 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr5:38945048 T>G maps to ENST00000296782 S1609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr10:5011015 C>T maps to NM_001353.5 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr16:70506484 A>G maps to NM_145059.2 E461E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr12:56365357 T>C maps to NM_001798.3 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr2:222301118 C>T maps to NM_004438.3 R782R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr17:16842992 G>A maps to NM_012452.2 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr2:216259361 G>A maps to NM_212482.1 Q1229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chrX:77225015 G>A maps to NM_001029891.2 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr9:80022519 C>A maps to ENST00000376646 A3158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr10:71264231 C>T maps to NM_012339.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr4:186329109 C>T maps to NM_018359.3 T367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr4:114214648 C>T maps to NM_001148.4 V810V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr5:118533573 C>A maps to NM_005509.4 T2556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr2:217724625 G>A maps to NM_003284.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr19:6731107 G>A maps to NM_001080452.1 G483G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr8:76463689 C>T maps to NM_004133.4 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr22:46760119 C>T maps to NM_014246.1 P2936P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr12:62902190 A>G maps to ENST00000393630 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr3:119133913 A>C maps to NM_020754.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr5:68660799 A>G maps to NM_001015892.1 D255D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr7:105641938 C>T maps to NM_152750.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr5:140729949 C>T maps to NM_018922.2 N41N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7169-01A-11D-2114-08 chr13:67205384 C>T maps to NM_203487.2 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr13:29242674 G>A maps to NM_015932.5 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr2:112702568 C>A maps to NM_006343.2 S172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chrX:15809136 G>T did not map to a codon.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr14:21790126 G>T maps to NM_020366.3 E576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr5:153765899 C>T maps to NM_198321.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr7:155255150 G>A maps to NM_001427.3 Q257Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr19:17394283 T>C maps to NM_152363.4 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7170-01A-11D-2114-08 chr19:46020998 G>T maps to NM_003370.3 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr16:66770147 C>T did not map to a codon.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr19:14204547 C>A maps to NM_002730.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr6:42713802 G>A maps to NM_003192.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr20:46279832 G>A maps to NM_181659.2 Q1253Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr10:52595832 C>A did not map to a codon.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr15:79748638 C>G maps to NM_015206.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr7:31378576 G>A maps to NM_022728.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr19:11447928 G>A maps to NM_004283.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr17:3181632 G>A maps to NM_002551.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr1:152538500 G>A maps to NM_178435.2 R62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr11:62289689 T>A maps to NM_001620.1 K4067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr11:407862 G>A maps to NM_021805.2 N145N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr6:53010373 A>G maps to NM_003643.3 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chrX:152037458 A>G maps to NM_015922.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr10:129905900 C>T maps to NM_002417.4 Q1401Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr12:81110949 G>T maps to NM_005593.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr19:50162973 G>A maps to NM_001571.5 S405S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr12:121434122 C>T maps to NM_000545.5 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HI-7171-01A-12D-2114-08 chr14:24040358 G>A maps to NM_032452.2 D527D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chrX:100513327 G>A maps to NM_001939.2 K807K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr1:153907308 C>T maps to NM_014856.2 Q900Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr15:74467264 C>T maps to NM_201526.1 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr17:48745030 C>A maps to NM_003786.3 G516G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr19:12126895 T>C maps to NM_001080411.1 A262A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr8:19218825 G>A did not map to a codon.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr2:125547650 G>A maps to NM_130773.2 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr1:220273971 T>C maps to NM_018060.3 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr11:74303720 T>G maps to NM_006591.1 Y6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8198-01A-11D-2260-08 chr8:98657099 G>A maps to NM_178812.3 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr14:52936857 C>G maps to NM_020784.2 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr1:179526350 G>A maps to NM_014625.2 D183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr8:89128917 T>G maps to NM_005941.4 R301R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr10:27381414 T>A maps to NM_014915.2 A186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr3:1394065 G>T maps to NM_014461.2 G475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr17:61776289 G>A maps to NM_030576.3 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-8200-01A-11D-A29Q-08 chr11:27077077 T>A maps to NM_003986.2 L34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr18:28986326 C>T maps to NM_001134453.1 L642L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr6:3113515 C>T maps to NM_003804.3 L653L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr2:239160326 C>A maps to NM_022817.2 E1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr19:22951197 G>A maps to ENST00000397104 I66I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr6:36887409 C>T maps to NM_152734.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr5:140574344 C>T maps to NM_018930.3 D740D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr1:165414094 G>T maps to NM_006917.4 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67K-01A-21D-A30E-08 chr9:116356366 C>G maps to NM_144489.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr19:56379185 C>T maps to NM_134444.4 G766G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr18:25565627 G>A maps to NM_001792.3 C613C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr4:81123566 G>A maps to NM_001099403.1 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr4:146823319 G>C maps to ENST00000508784 S364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr1:167823645 A>C maps to NM_018417.4 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr16:88688650 C>T maps to ENST00000452588 Q532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr4:62758467 G>A maps to ENST00000506720 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr4:122723879 A>C maps to NM_001034194.1 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr5:140209376 G>A maps to NM_018909.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr19:43233350 G>A maps to NM_021016.3 S389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr1:158325303 C>T maps to NM_030893.3 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr16:88688649 G>C maps to ENST00000452588 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr4:84377253 C>T maps to NM_016067.2 C8C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67L-01A-11D-A30E-08 chr12:22354691 C>A maps to NM_003034.3 E289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr20:55914069 G>A maps to ENST00000371258 K301K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr5:101795411 G>A maps to NM_173488.3 V323V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr11:18267019 C>T maps to NM_030754.4 A91A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr5:74641423 T>C maps to NM_000859.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr17:43311098 G>A did not map to a codon.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr4:62903475 C>T maps to ENST00000506720 R1207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr15:64365168 T>C maps to NM_032231.4 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr2:10350626 G>A maps to NM_182626.1 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr21:22804446 T>A maps to NM_004540.2 Y500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr8:89068387 G>A maps to NM_005941.4 D447D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr21:34058197 A>G maps to NM_003895.3 A365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr22:21213457 C>T maps to NM_004782.3 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr7:148701023 G>A maps to NM_004911.4 F600F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr1:159505650 G>A maps to NM_001004469.1 I49I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr5:45262466 C>T maps to NM_021072.2 P743P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr2:11053085 G>A maps to NM_002236.4 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr4:39522979 A>G maps to NM_003359.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr19:726158 G>A maps to NM_002579.2 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr2:219259417 G>T maps to NM_000578.3 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr7:114270014 A>G maps to NM_148898.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chrX:91133812 C>T maps to NM_032968.3 N858N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr19:40357400 C>A maps to NM_003890.2 T5304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr4:62812713 G>A maps to ENST00000506720 T834T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr4:23886555 T>C did not map to a codon.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr3:36873597 C>A maps to NM_014831.2 L2448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr5:6748611 C>T maps to NM_006999.4 Q249*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr15:56657674 G>C maps to NM_198524.1 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67N-01A-11D-A30E-08 chr5:153144158 G>A maps to NM_001114183.1 T663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr10:91371707 C>G maps to NM_148977.1 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr1:90178509 C>T maps to NM_032270.4 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr13:92345963 G>A maps to NM_004466.4 A283A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr16:87788844 G>T maps to NM_017566.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr6:29395334 C>T maps to NM_013937.2 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr11:64559402 C>T maps to NM_004579.2 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr14:103416202 G>T maps to NM_006035.3 R1116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67O-01A-11D-A30E-08 chr7:150699373 T>C maps to NM_000603.4 D578D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr8:2021548 C>T maps to NM_003970.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr14:20344653 C>T maps to NM_001005501.1 F76F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr10:72498707 C>T maps to NM_139155.2 G573G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr18:56246843 C>T maps to NM_052947.3 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr16:570796 G>A maps to NM_014700.3 V743V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr21:38114058 C>T maps to NM_005069.3 L298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr1:204951035 C>T maps to ENST00000367172 Y786Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr7:72988434 T>A maps to NM_012453.2 I93I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67Q-01A-21D-A30E-08 chr6:43275383 G>C maps to ENST00000449267 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr15:75013054 A>T maps to NM_000499.3 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr6:6224991 T>C maps to NM_000129.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr2:131976469 C>T maps to NM_001083538.1 D165D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr22:50682699 T>C maps to NM_020461.3 K63K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr5:176310789 G>A maps to NM_002115.2 C678C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr1:158151488 C>T maps to NM_001766.3 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr11:47857210 G>A maps to NM_015231.1 R365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr14:21623155 C>T maps to NM_001004731.1 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr4:96762204 C>T maps to NM_005390.4 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr10:134158048 G>T maps to NM_030626.2 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr13:51825913 C>T maps to NM_145019.2 H173H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67R-01A-21D-A30E-08 chr19:14199509 C>T maps to ENST00000269724 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr21:30963506 C>T maps to ENST00000327783 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr16:30715428 C>T maps to NM_006662.2 A33A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr1:43296725 C>T maps to NM_018538.3 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr11:78277281 C>A maps to NM_024678.4 E137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr22:38165191 C>T maps to NM_001039141.2 Q2245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr10:73544679 C>T maps to ENST00000398860 N1850N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr3:167217985 C>A maps to NM_178824.3 E644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67S-01A-11D-A30E-08 chr17:38938514 G>A maps to NM_181537.3 H77H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr4:109767342 G>A maps to ENST00000333642 D489D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr13:29599578 C>T maps to NM_001033602.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr2:209307105 C>T maps to NM_005048.2 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr3:109050825 C>T maps to NM_018189.3 K77K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr2:136558281 G>A maps to NM_002299.2 R1587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr5:140474538 G>T maps to NM_018936.2 G55G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr12:43944935 G>A maps to ENST00000389420 R77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A67T-01A-11D-A30X-08 chr10:134261456 C>G maps to NM_173541.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr2:233899739 C>A maps to NM_005383.2 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr1:186106991 C>T maps to NM_031935.2 R4604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr1:31189119 G>A maps to NM_002379.3 D281D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr19:19576171 C>T maps to ENST00000404158 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr7:100320665 T>G maps to NM_000799.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G1-01A-11D-A30X-08 chr3:50340315 G>T maps to NM_153281.1 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr7:135279305 T>C maps to NM_015135.2 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr1:11169350 G>T maps to NM_004958.3 L2508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr15:22933657 G>T did not map to a codon.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr17:72736965 C>T maps to NM_001006638.2 D51D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr5:132158688 C>T maps to NM_001172700.1 L786L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr4:155509999 A>G maps to NM_000508.3 H103H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chrX:128599495 C>T did not map to a codon.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr7:92734006 T>C maps to NM_017654.3 V468V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6G3-01A-11D-A30X-08 chr12:56492615 C>T maps to NM_001982.2 D922D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr15:33795932 C>T maps to NM_001036.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr12:114841631 G>A maps to NM_000192.3 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr20:54823919 G>T maps to ENST00000371389 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr5:32089673 G>A maps to NM_178140.2 A2040A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr17:40843293 C>T maps to NM_003632.2 D733D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr6:149700268 A>G maps to NM_015093.4 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr10:18429691 G>T maps to NM_201596.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr6:136599813 G>A maps to NM_014739.2 R69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J4-A6M7-01A-11D-A31L-08 chr22:38823054 C>G maps to NM_152868.1 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr15:100269695 G>A maps to NM_152449.2 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr8:77895774 G>A maps to NM_001172087.1 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr13:37401781 G>A maps to NM_000538.3 S237S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr5:54771250 G>T maps to NM_003711.2 S29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr1:8390701 C>T maps to ENST00000377479 G417G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr1:24075566 G>A maps to NM_003198.2 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr17:7811745 G>T maps to NM_001005271.2 E1786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr4:104065637 C>G maps to NM_001813.2 T1665T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52B-01A-11D-A26M-08 chr9:113312164 C>A maps to ENST00000374463 E251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:95502187 A>G maps to NM_015496.3 L1755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:74091249 G>A maps to ENST00000443185 G940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:76028838 C>T maps to NM_001992.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:33236869 G>A maps to NM_022553.4 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:46638333 A>G maps to NM_024745.4 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:86106420 A>C maps to NM_001156474.1 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:128488071 C>T maps to NM_001458.4 D1510D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:24031219 G>A maps to NM_003917.2 Q562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:58722739 G>A maps to NM_080661.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:52481973 C>T maps to NM_007361.3 P1016P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:56713244 C>T maps to NM_001127460.2 S1043S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:38835667 T>C did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:27689213 C>T maps to NM_015202.2 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:118487709 C>T maps to NM_005509.4 R1561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:113558763 C>T maps to NM_002711.3 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:50994312 G>A maps to NM_005215.3 S1223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:75053836 C>T maps to ENST00000257665 W523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:23543821 A>G maps to NM_003430.2 T653T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:145535420 C>T maps to NM_005526.2 Y253Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:96761272 G>A did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:61924007 C>T maps to NM_006255.3 R359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chrX:5821329 G>A maps to ENST00000381093 Y483Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:30315488 C>T maps to NM_020848.2 L1196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:61305231 C>T maps to NM_002974.2 T298T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chrX:151869696 G>A maps to NM_005363.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:5743013 G>A did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:17418972 G>A maps to NM_007365.2 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:84104351 G>A maps to NM_003791.2 N541N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:2030957 G>A maps to NM_172168.1 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:22390047 C>T maps to NM_145290.2 T1082T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:40319623 C>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:151109505 G>A maps to NM_001178061.1 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:150034681 G>A maps to NM_023942.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:103335661 G>A maps to NM_032718.3 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:775121 C>T maps to NM_001031737.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:95869989 G>A maps to NM_032310.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:179588312 T>G maps to NM_133378.4 R5928R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:56575859 G>A maps to NM_003075.3 Y212Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:23712399 G>A maps to NM_033266.3 S461S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:15175096 C>T maps to NM_152574.2 P626P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:40433638 C>T maps to NM_003890.2 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:32964314 G>A maps to NM_207313.1 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:96963421 G>A maps to NM_014014.3 R386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:170048427 G>A maps to NM_004525.2 Y2982Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chrX:69370143 G>A maps to NM_001551.2 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:100123402 C>T maps to NM_001127258.1 D323D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:5274308 C>T maps to NM_002850.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:11630113 G>A maps to ENST00000423059 Q476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:9746374 T>G maps to NM_015055.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:51064978 G>A maps to NM_173602.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:5140530 C>T maps to NM_201400.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:180324130 C>T maps to NM_133462.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:95034588 C>T maps to NM_006215.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:137321059 C>T maps to NM_002957.4 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:12540984 A>G maps to NM_005815.4 H667H. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-J9-A52C-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:36298374 C>T maps to NM_001010903.4 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:177036518 G>A maps to NM_006898.4 P272P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-J9-A52C-01A-11D-A26M-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:16254790 A>G did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:46721967 G>A maps to NM_147129.3 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:33171400 C>T maps to NM_006979.2 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:35345869 C>T maps to NM_012138.3 R334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:114466494 T>A maps to NM_018700.3 G542G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:57175885 G>A maps to NM_001005850.1 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:124988245 G>A maps to NM_001039112.2 A264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:101661555 G>A maps to NM_152628.3 D29D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:98608823 G>A maps to ENST00000359863 A3682A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:123426764 G>A maps to NM_053025.3 C742C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr22:30125183 C>A maps to NM_182527.2 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:22006440 G>A maps to NM_139278.2 Y293Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:72157463 G>A maps to NM_031293.2 Q892*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:179025749 C>T maps to NM_025158.3 R563R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:129910062 A>T maps to NM_002417.4 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:55341681 G>A maps to NM_013289.2 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:65366865 G>A maps to NM_002419.3 R735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:160494344 T>C maps to NM_000876.2 P1597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:127956951 C>T maps to NM_001001665.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:89350060 G>A maps to NM_013275.4 D963D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:93624976 G>A maps to NM_000313.3 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:76397715 G>A maps to NM_080868.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:5550837 C>T maps to NM_019593.3 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:107309879 C>T maps to NM_152434.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:116718255 C>T maps to ENST00000445177 S1289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:148586655 C>T maps to NM_014945.2 C178C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:17943478 C>T maps to NM_000215.3 P843P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:47955074 T>C maps to NM_138295.3 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:156746768 G>T did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:71536661 G>A maps to NM_203350.2 D177D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:101586125 G>A maps to NM_152628.3 C430C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:30627569 C>T maps to NM_003587.4 V599V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:17800326 G>A maps to NM_022113.4 H824H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr15:34150102 C>T maps to NM_001036.3 D4710D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:6959467 G>A maps to NM_005559.2 I2550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:130059741 G>A maps to NM_021978.3 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:204409440 G>A maps to NM_002646.3 D1086D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:65107960 C>T maps to NM_006268.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:1256377 C>T maps to ENST00000447027 Y901Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:210796907 C>T maps to NM_001170580.1 H428H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:75199712 G>A maps to NM_001039573.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:130010332 C>T maps to NM_001642.2 A638A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:1234614 C>T maps to ENST00000382477 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:154557715 G>A maps to ENST00000292205 D1183D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:118198838 G>A maps to ENST00000339824 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:49224878 G>A maps to NM_024603.2 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:66753716 T>C maps to ENST00000401827 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:58022501 G>A maps to NM_001478.3 F332F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:128034366 C>T maps to NM_000883.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:62078120 C>T maps to NM_172107.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:138707775 C>T maps to ENST00000409386 A1460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:21903984 C>T maps to NM_000478.4 G473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:35471597 C>T maps to NM_003322.3 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:26455001 C>T maps to NM_017433.4 Y1002Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:66852501 G>A maps to ENST00000359087 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:138714574 G>A maps to ENST00000409386 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:2273483 C>T maps to NM_020972.2 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:148886178 C>T maps to NM_024605.3 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:41774067 G>A maps to ENST00000373009 D218D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:145006672 G>A maps to NM_201380.2 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:100170917 G>A maps to NM_001025108.1 N1163N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:17699168 C>T maps to ENST00000395776 D969D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:228487116 C>T maps to ENST00000366707 D1146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:24545426 C>T maps to NM_006032.2 R332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:76755233 C>T maps to NM_171999.2 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:222347369 G>A maps to NM_004438.3 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:54886367 G>A maps to NM_003128.2 T2107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:6438669 G>A maps to NM_001065.3 N392N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:61819477 G>A maps to ENST00000503366 S1682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:139289315 G>A maps to NM_003086.2 N162N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:65303715 A>G maps to NM_002227.2 S1013S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:27310661 G>A maps to NM_004103.3 P860P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:71216680 C>T maps to NM_033141.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:11224017 C>T maps to NM_000527.4 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:156825202 C>T maps to NM_005651.2 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:15580622 G>A maps to NM_052890.3 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:150297486 G>A maps to NM_004698.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr13:103297266 G>A maps to ENST00000376052 S767S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:6925364 G>A maps to NM_001113361.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:58005260 C>T maps to NM_001098491.1 R447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:39229796 G>A maps to NM_194293.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:43748502 C>T maps to NM_001025366.2 R333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:116984537 C>T maps to NM_032888.2 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:158483058 G>A maps to NM_003898.3 T330T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:233190172 G>A maps to NM_014801.3 Q1398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:41700462 C>T maps to ENST00000301173 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:51897157 G>A maps to NM_203424.1 R89R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:5755632 G>A maps to NM_153717.2 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:56487294 C>T maps to NM_001982.2 R481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:30625114 G>T maps to NM_138328.2 E225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:97078468 G>A maps to ENST00000342887 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:1005551 G>A maps to NM_138690.1 K684K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:68675743 C>T maps to NM_002180.2 R130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chrX:1743282 C>T maps to NM_001171038.1 D122D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:169629714 G>A maps to NM_003247.2 G737G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:61288117 C>T maps to NM_016354.3 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:34171787 T>C maps to NM_139215.1 G495G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:22172691 G>A maps to NM_005529.5 Y2791Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:74392305 G>A maps to NM_022066.3 S904S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:226551699 C>T maps to NM_001618.3 T910T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:148875782 G>A maps to NM_170686.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:28620206 G>A did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:100390835 G>A maps to NM_032503.2 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:130021607 G>A maps to NM_001868.2 S95S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr15:89453091 G>A maps to NM_005928.2 R46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:61834853 C>T maps to NM_017798.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:137191047 G>A maps to NM_000288.3 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:217297569 C>T maps to NM_014140.3 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:176526075 G>A maps to NM_020318.2 A206A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:149460504 G>A maps to NM_005211.3 G44G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:238494710 G>A maps to NM_022449.3 S29S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:92146658 T>C maps to NM_000466.2 G390G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:231299692 C>T maps to NM_001004342.3 C326C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:1405753 C>T maps to NM_018702.2 A182A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:26031877 T>C maps to NM_003537.3 *137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr15:91433507 G>A maps to NM_002005.3 S412S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:22006195 G>A maps to NM_004936.3 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:56485249 C>T maps to ENST00000281662 K1758K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:140203081 C>T maps to NM_018908.2 G574G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:129974997 C>T maps to NM_014636.2 H482H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:15535751 G>A maps to ENST00000389282 G1424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:52887681 T>A maps to NM_001145434.1 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:20418788 C>T maps to NM_002214.2 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr6:16279024 C>T maps to NM_006877.3 C186C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:175372582 G>A maps to NM_003285.2 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:8612973 G>A maps to NM_012335.3 F405F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:136969759 G>A maps to NM_017415.2 Y472Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:49236608 G>A maps to NM_080829.2 Y57Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:73559542 C>T maps to NM_001031803.1 Y275Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chrX:1561135 C>T maps to NM_004192.3 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:45888874 G>A maps to NM_001142502.1 F731F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:112604724 G>A maps to NM_022662.2 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:10255193 C>T maps to NM_001570.3 I250I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr18:3215101 G>A maps to NM_003803.3 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:27216197 T>C maps to NM_018066.3 Q130Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:18638607 C>T maps to NM_001037330.1 G294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:131381260 C>T maps to NM_001130438.2 G1904G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:73433349 C>T maps to NM_015009.1 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:3235011 C>T maps to NM_002111.6 D2796D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:76045217 C>T maps to NM_001142640.1 G25G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:79898328 G>A maps to ENST00000376646 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:150417943 C>T maps to NM_130759.3 G284G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr19:55086795 G>A maps to NM_001130917.1 Q243Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:24994193 G>A maps to NM_032501.2 D519D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:140741804 G>A maps to NM_018923.2 V701V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr15:75047380 C>T maps to NM_000761.3 H501H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr10:75888896 G>A maps to NM_207012.2 R258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:29884627 G>A maps to NM_201575.2 G807G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr16:1536524 G>A maps to NM_001013658.1 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:1164337 C>T maps to NM_012445.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:65260130 G>A maps to ENST00000389723 G754G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr21:38862609 G>A maps to NM_001396.3 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:103040430 C>T maps to NM_003853.2 N77N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:140751253 G>A maps to NM_018924.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:17438496 G>A maps to ENST00000302539 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chrX:153033810 C>T maps to NM_005393.2 S398S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr22:37455444 C>T maps to ENST00000403888 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:133540273 C>T maps to NM_207363.2 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:122160928 G>A maps to NM_002264.3 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:65635812 G>A maps to NM_016938.3 C309C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:230725183 A>G maps to ENST00000389044 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:140222183 C>T maps to NM_018911.2 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr14:62200949 T>C maps to ENST00000394997 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:42275595 T>C maps to NM_016004.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr13:95121165 G>A maps to NM_001129889.1 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr9:71628906 G>A maps to NM_002732.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr20:33589833 G>A maps to NM_020884.3 A1962A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:6125267 G>A maps to NM_000552.3 A1814A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr5:14504648 C>T maps to NM_007118.2 V2853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr4:3318862 C>T maps to NM_198229.2 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr8:22862015 C>T maps to NM_001160036.1 N45N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:31906940 G>A maps to NM_178865.4 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr12:109693957 G>A maps to NM_001093.3 T2060T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr3:124132333 C>T maps to NM_001024660.3 D786D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr7:122342453 G>A maps to NM_198085.1 N117N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr2:232196542 C>T maps to ENST00000359743 D604D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr17:58700882 G>A maps to NM_003620.3 A158A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr22:44371975 C>T maps to NM_015380.4 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:55111452 C>A maps to NM_001005274.1 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr1:156937787 G>A maps to NM_198236.1 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr10:50953975 C>T maps to NM_018245.2 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr13:36402389 G>T maps to NM_004734.4 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr19:51330398 C>G maps to NM_017509.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr9:128230299 G>A maps to NM_001006617.1 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr17:76566364 G>T maps to ENST00000389840 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr4:167020675 C>T maps to ENST00000507499 S991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr20:62572024 G>A maps to NM_017859.3 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr14:24632647 G>A maps to NM_006084.4 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr17:76472713 G>A maps to ENST00000389840 D2684D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr2:15432833 G>A maps to NM_015909.2 H1618H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chr5:33937287 G>A maps to NM_016568.3 W148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52D-01A-11D-A29Q-08 chrX:49955713 T>A maps to NM_003886.2 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr2:128262755 C>T maps to NM_017969.2 E241E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr9:90296531 A>T maps to NM_004938.2 K739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr10:125426387 G>A maps to NM_153442.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr1:159166232 C>T maps to NM_021189.3 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr6:27777904 C>A maps to NM_003536.2 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr10:63525767 C>G maps to NM_173554.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr3:111719773 G>A maps to NM_001008272.1 Q112Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr19:45211202 C>T maps to ENST00000396750 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J9-A52E-01A-11D-A26M-08 chr7:134849231 G>A maps to NM_018295.3 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr17:39383025 C>T maps to NM_031961.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr8:145094891 C>T maps to NM_198572.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr2:232320220 A>G maps to NM_005381.2 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr1:156845393 C>T maps to NM_002529.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr4:154709576 G>A maps to NM_003013.2 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr5:149602667 G>A maps to NM_015981.3 D450D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr1:220213573 G>A maps to NM_004446.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr5:118837733 A>G did not map to a codon.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr19:52496291 C>T maps to ENST00000354939 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr6:143828560 C>T maps to NM_032020.4 W75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BL-01A-31D-A257-08 chr1:94497573 G>A maps to NM_000350.2 N1296N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr1:1654057 C>T did not map to a codon.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr20:13695682 T>C maps to NM_016649.3 E798E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr1:158984676 C>T maps to ENST00000295809 F69F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr8:95952350 C>T maps to NM_033285.3 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr5:178310628 C>T maps to NM_058230.2 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BO-01A-61D-A257-08 chr19:48807366 C>A maps to NM_144577.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BR-01A-32D-A257-08 chr1:16727314 C>A maps to NM_198546.1 R358R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BR-01A-32D-A257-08 chr11:123886817 C>T maps to NM_001004462.1 D179D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr17:73836335 G>A maps to ENST00000412096 C276C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chrX:16142273 T>C maps to NM_005314.2 C66C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr15:45433154 G>A maps to NM_175940.1 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr5:140432440 A>C maps to NM_013340.2 R462R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BV-01A-31D-A26M-08 chr17:11687705 C>T maps to NM_001372.3 L2637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:207025332 T>C maps to NM_021121.3 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:34517404 C>T maps to NM_012144.2 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chrX:149831995 C>T maps to NM_000252.2 R520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:27420590 G>T maps to NM_007149.2 P249P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:10503680 G>A maps to NM_000480.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:1470988 G>A maps to NM_024830.3 V410V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:37730603 G>A maps to NM_001002814.2 G572G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:2691854 C>T maps to NM_025250.2 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:32200865 C>T maps to NM_001136029.1 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:1192811 G>A maps to ENST00000401903 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:89245891 G>A maps to NM_004933.2 A37A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:2891120 C>T maps to NM_032048.2 G332G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:89912188 C>T maps to NM_014883.2 K180K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:24473883 G>A maps to NM_001503.2 H151H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:29708605 C>T maps to NM_014298.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:37234283 G>A maps to NM_020405.4 C356C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:151340693 G>A maps to ENST00000435071 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:176638165 G>A maps to NM_022455.4 T922T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:79396693 C>T maps to NM_025074.6 T2595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:46921855 G>A maps to ENST00000256991 D136D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chrX:99662412 G>A maps to NM_001184880.1 R395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:112318869 G>A maps to ENST00000315987 D599D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:7756413 C>T maps to NM_001080424.1 D1569D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:1673174 G>A maps to NM_002615.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:31683137 G>A maps to NM_194300.2 S718S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:170669732 C>T maps to NM_022897.3 L895L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:117106078 G>A maps to NM_030767.4 H1222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:60615457 C>T maps to NM_024098.3 R274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:126080680 C>T maps to NM_012259.2 C249C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:46056804 G>A maps to NM_025136.3 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:102946625 T>C maps to NM_017935.4 A518A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:39544512 G>A maps to NM_207445.2 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:128807690 G>A maps to NM_178562.3 Q276Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:150444463 A>T maps to NM_015203.3 K1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:35579044 C>T maps to NM_024772.3 D538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:149853787 C>T maps to NM_004522.1 H678H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:27285094 C>T maps to NM_178860.4 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:17270254 C>T maps to NM_004145.3 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:56467958 C>T maps to NM_001013358.1 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:85589837 C>T maps to NM_145172.3 D672D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:13230973 C>T maps to NM_182751.2 R438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:151105901 G>A maps to NM_001178061.1 G649G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:733030 C>T maps to ENST00000293882 T282T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:68610373 G>T maps to NM_000406.2 C218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:380293 C>T maps to NM_178537.4 D906D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:139350602 G>A maps to NM_014866.1 R1856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:42281463 C>T maps to NM_015559.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:909721 C>T maps to ENST00000379409 P612P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:156957867 C>T maps to ENST00000430702 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:89744488 G>A maps to NM_001946.2 N238N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:3532473 G>A maps to NM_001136198.1 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:2796318 C>T maps to NM_080739.2 D132D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:15366906 C>T maps to NM_058243.2 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:85101006 G>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:42363729 G>A maps to NM_178034.3 F531F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:79954526 G>A maps to ENST00000306729 S246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:11185820 T>C maps to NM_006403.3 L693L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:71524027 T>C maps to ENST00000515404 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:33157147 G>A maps to NM_080680.2 R61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:21330572 C>T maps to NM_144704.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:39521646 C>T maps to ENST00000394004 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:33459801 C>T maps to ENST00000455217 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:94898625 G>A maps to NM_001166160.1 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:61914293 G>C maps to NM_001040694.1 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:35916051 C>T maps to NM_024874.4 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:126723742 C>T maps to NM_032242.3 D545D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:27688650 G>A maps to NM_015662.1 I597I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:108391472 C>T maps to NM_014648.3 N853N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:30094418 G>A maps to ENST00000440706 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chrX:65413404 C>T maps to NM_138737.3 R486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:52882149 G>A maps to NM_005554.3 I462I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:43916457 G>A maps to NM_001077663.1 C868C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:22140591 A>G maps to NM_001135721.1 G157G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:122811250 G>A maps to NM_006810.3 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr21:31692134 G>A maps to NM_203405.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:2336813 G>A maps to NM_001089.2 A1053A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:4828124 C>T maps to NM_144605.3 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:111426771 G>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:14927706 G>A maps to NM_177925.2 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:18916804 G>A maps to NM_152351.3 K371K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:6519837 C>A maps to NM_144666.2 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:61175176 C>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:95091241 C>T maps to NM_014899.3 C275C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:91769873 C>T maps to NM_014848.4 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:36211632 C>T maps to NM_007096.3 D203D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:10570422 G>A maps to NM_001111307.1 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:63543656 G>A maps to NM_000706.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:123419104 G>A maps to NM_053025.3 D1070D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:35176564 C>T maps to NM_006097.3 N105N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:128781962 C>T maps to NM_000890.3 D265D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:3339478 C>T maps to NM_005741.4 R325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:28386875 C>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:34381367 G>A maps to NM_032596.3 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:107602599 G>A maps to NM_005502.3 G338G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:134218870 C>T maps to NM_138499.3 D289D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:47649197 C>T maps to NM_153839.6 N233N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:152127347 G>A maps to NM_001122965.1 R743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:54526455 C>T maps to NM_153228.2 D375D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:30002648 G>A maps to NM_004783.2 P970P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:130198256 C>T maps to NM_007135.2 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:61492926 C>T maps to ENST00000389520 Y1279Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:1067392 G>A maps to NM_001131034.3 R190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:165962456 A>G maps to NM_152620.2 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:233621022 C>T maps to ENST00000373566 R120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:41062194 C>T maps to NM_002505.4 R317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr13:32914548 C>T maps to NM_000059.3 N2019N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:84884583 C>T maps to NM_014895.2 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:55362954 G>A maps to NM_024335.2 A355A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:9528610 C>T maps to NM_003887.2 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:86007449 G>A maps to ENST00000358110 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:154412195 C>T maps to NM_001145279.1 T344T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:148701134 G>A maps to NM_004911.4 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140750488 G>A maps to NM_018924.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:60754669 C>T maps to NM_006039.3 S625S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:73498256 G>A maps to NM_020753.3 P966P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:55127502 G>A maps to NM_006206.4 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:90451587 G>A maps to ENST00000398333 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:72277950 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:91406184 C>T maps to NM_201269.1 T242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:120156516 G>A maps to ENST00000392521 S1330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:205210850 C>T maps to NM_014858.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:52681013 G>A maps to NM_002281.3 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:25149159 C>T maps to NM_001101339.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr14:99641822 C>T maps to NM_138576.2 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:80548555 C>T maps to NM_001825.2 A65A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chrX:37028756 C>T maps to NM_001013736.2 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:113057603 C>T maps to NM_024494.2 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:44100940 C>T maps to NM_022437.2 N409N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:4902801 G>A maps to NM_001080523.1 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:141356217 G>A maps to NM_018557.2 Y2392Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:44278576 C>T maps to NM_002250.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:45448006 G>A maps to NM_175940.1 T1194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:113875850 G>A maps to NM_138432.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:41900302 C>T maps to NM_004053.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:122078449 G>A maps to NM_001167940.1 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:184099096 G>A maps to NM_003741.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:124416489 C>A maps to NM_207437.3 A4259A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:46836914 G>A maps to NM_001001436.2 V138V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:30491787 G>A maps to NM_006092.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:12767771 C>T maps to NM_000528.3 T506T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:124824935 G>A maps to NM_006312.4 R1805*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:31473605 G>T maps to ENST00000408912 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:142222364 G>A maps to NM_001080431.1 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:155711422 G>A maps to NM_002239.2 S368S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:58108881 C>T maps to NM_001164317.1 I1063I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:5462083 G>A maps to NM_015325.1 R879R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:205498651 G>A maps to NM_212503.2 L424L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:153830730 C>T maps to NM_024632.5 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:3567065 G>A maps to NM_014604.2 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:44015715 C>T maps to NM_014297.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:152484039 G>A maps to NM_001164507.1 S3380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:40034430 G>A maps to ENST00000401700 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:42572368 C>T maps to NM_004624.3 A245A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chrX:153587695 G>A maps to NM_001110556.1 D1407D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:122359384 C>T maps to NM_144668.4 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:34945825 G>A maps to NM_024835.3 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:43907567 C>T maps to NM_001145146.1 H210H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:1267115 G>A maps to ENST00000447027 T3005T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:58198230 C>T maps to ENST00000356715 H196H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:64698333 T>C did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:65124394 G>A maps to NM_145719.2 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:73482397 G>A maps to ENST00000375248 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:142399949 G>A maps to NM_002511.2 S171S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140712515 C>T maps to NM_018912.2 H755H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:65303494 G>A maps to NM_020680.3 A486A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr15:25953222 G>A maps to NM_024490.3 C825C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:170099967 C>T maps to NM_004525.2 S1165S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:100490934 G>A maps to NM_000665.3 R307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:148756444 C>T maps to NM_014443.2 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:73152134 C>T maps to ENST00000419692 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:223489481 G>A maps to NM_005687.3 R305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:18622251 C>T maps to NM_001040272.4 C162C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:29996667 G>A maps to NM_016151.2 E519E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:720195 G>A maps to NM_022772.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:43687178 G>A maps to NM_173050.2 D119D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:106814358 C>T maps to NM_012082.3 D683D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:201618017 C>T maps to ENST00000367296 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:11158105 G>A maps to NM_001001998.1 C73C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:202245768 G>A maps to NM_015049.2 R748*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:13249042 C>T maps to NM_052876.2 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:12131157 C>T maps to NM_018706.5 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:72776114 C>T maps to NM_017757.2 I2146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:12901216 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:104230505 G>A maps to NM_024789.3 S112S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:2025081 C>T maps to NM_006453.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:27630136 C>T maps to ENST00000319394 G498G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:133949507 C>T maps to NM_001105521.2 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:135275596 G>A maps to NM_007344.2 S472S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:72211429 G>A maps to NM_000503.4 Y226Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:130949670 C>T maps to NM_207312.2 V362V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:41608015 C>T maps to NM_014988.2 R161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:43024049 G>T maps to NM_015950.3 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140516575 C>T maps to NM_015669.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:100212598 G>A maps to NM_023948.4 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:21156619 G>A maps to NM_017539.1 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:25611101 G>A maps to NM_021907.3 V568V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:34262434 G>A maps to NM_021100.4 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:69002946 G>A maps to NM_024870.2 T749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:40849590 G>A maps to NM_003632.2 P1196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:26463096 G>T maps to NM_017433.4 E1302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:55036726 C>T maps to ENST00000357530 S180S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:76756937 C>T maps to NM_171999.2 G1173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:201324530 T>C maps to ENST00000409151 D284D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:231742221 C>T maps to NM_030926.4 N223N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:1780294 G>A maps to NM_001909.3 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:18507626 G>A maps to NM_145256.2 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:121188335 G>A maps to NM_177478.1 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:193377283 T>C maps to NM_130837.2 I818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:1268945 C>T maps to ENST00000447027 P3615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:128973690 C>T maps to NM_001039762.2 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:228210433 G>A maps to ENST00000366753 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:11317935 C>T maps to NM_152391.3 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:99690697 G>A maps to NM_005916.3 R673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140229396 C>A maps to NM_031857.1 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:72829830 C>T maps to NM_006885.3 T2250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:85818985 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr14:59965594 C>T maps to ENST00000356057 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:607295 C>A maps to ENST00000264555 R614R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:7682661 C>T maps to NM_020877.2 A1881A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:104117886 A>G maps to NM_020978.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:4496342 C>T maps to ENST00000301284 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:16360534 G>A maps to NM_024704.4 R704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:118199030 C>T maps to ENST00000339824 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:39373860 C>T maps to NM_005201.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:155649576 C>T maps to NM_003875.2 Y528Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:121251941 G>A maps to ENST00000393672 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:24574973 A>G maps to NM_006910.4 P503P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:121528317 G>A maps to NM_022045.3 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:100479772 G>A maps to NM_015908.5 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:118984806 C>T maps to NM_014807.3 D548D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr21:40193594 C>T maps to NM_005239.4 D387D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:38041480 C>T maps to NM_018957.3 C296C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:127336183 G>A maps to NM_004526.2 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:12638261 A>C maps to NM_144976.3 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:27437498 C>T maps to NM_078471.3 A1014A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:117103925 C>T maps to NM_030767.4 S1318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:53073992 G>A maps to NM_014682.2 F512F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr13:101717892 G>A maps to NM_052867.2 R1489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr7:82581481 G>A maps to NM_033026.5 P2929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:135073795 C>T maps to NM_032536.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:40711064 C>T maps to NM_002446.3 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:124535155 C>T maps to ENST00000408936 A783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:71748730 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:162680659 G>A maps to NM_020116.3 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:114719 C>T maps to NM_022450.3 T75T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:43568520 G>A maps to NM_015140.3 R461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:4516289 G>A maps to NM_020677.3 D131D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:101552590 G>A maps to ENST00000375018 H219H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr3:48559454 G>A maps to NM_004567.2 N438N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:37316001 G>A maps to NM_000831.3 D412D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:54663421 C>T maps to NM_024316.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:170725810 G>A maps to NM_022897.3 A1072A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:145038027 G>A maps to NM_002099.6 Y112Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:12800211 G>A maps to ENST00000380339 R456*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:241402906 C>T maps to NM_002081.2 D287D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr14:75558140 G>A maps to NM_033116.4 G758G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:45260308 G>A maps to NM_005178.4 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:123319047 G>A maps to NM_001010852.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:22884791 G>A maps to NM_003842.4 R264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:2116220 C>T maps to ENST00000355272 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:39973357 C>A maps to NM_021939.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:130648818 C>T maps to NM_007197.3 I444I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140249998 G>A maps to NM_018902.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:90180447 C>T maps to NM_032270.4 D773D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:122213654 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:39883621 C>A maps to NM_001098270.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:15145384 G>A maps to NM_183005.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr14:86088043 G>A maps to NM_013231.4 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:105362574 C>T maps to ENST00000369774 S800S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:72462204 C>T maps to NM_139155.2 D220D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr16:23707240 G>A maps to NM_033266.3 R576R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:89577166 C>T maps to NM_014606.1 G350G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:28654829 G>A maps to ENST00000438199 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:16143928 G>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:153913418 C>T maps to NM_014856.2 R429R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:126373018 G>A maps to NM_024582.4 T3616T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:218614598 C>T maps to NM_001135599.2 C408C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr12:6161935 C>T maps to NM_000552.3 P653P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:87041172 C>T maps to ENST00000263723 Y614Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:50905528 C>T maps to ENST00000391817 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:10290658 C>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:55193499 G>A maps to ENST00000427138 A812A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr14:32142776 G>A maps to NM_025152.2 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:22161190 G>A maps to NM_005529.5 H3567H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:49363680 G>A maps to NM_020904.2 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:54876763 C>T maps to NM_003128.2 R1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr2:157186311 C>T maps to NM_006186.3 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:32500780 T>C maps to NM_000343.3 R558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr10:71883672 G>A maps to NM_032797.5 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:20005665 G>A maps to NM_000871.1 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:37211238 G>A maps to NM_002854.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:45740516 G>A maps to NM_148674.3 R1210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:50408259 G>A maps to NM_020436.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:120008241 G>A maps to NM_012101.3 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr22:32234676 C>T maps to NM_001136029.1 D778D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:80274163 C>T maps to NM_006137.6 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:131832159 C>T maps to NM_032809.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:233190116 G>A maps to NM_014801.3 G1416G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:20107640 C>T maps to NM_021020.2 A461A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140182314 C>T maps to NM_018906.2 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chrX:77150898 C>T maps to NM_032121.5 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr9:136083532 G>A maps to NM_014581.2 G88G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:771081 G>A maps to NM_182612.2 H189H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:154321479 G>A maps to NM_020452.3 A1186A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr17:2280071 C>T maps to NM_014853.2 C885C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:90400075 C>T maps to NM_001134479.1 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr11:62455620 G>A maps to NM_203422.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:2573007 C>T maps to NM_006101.2 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr20:25472046 G>A maps to NM_025176.4 D475D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:112327914 T>C maps to NM_152624.4 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr4:187130277 C>T maps to ENST00000511608 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr1:23234627 C>T maps to ENST00000400191 D773D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr21:43693445 C>T maps to NM_004915.3 N146N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chrX:70613206 A>G maps to ENST00000449580 E1035E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:5245856 C>T maps to NM_002850.3 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr8:77766737 G>A maps to NM_024721.4 P2527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr6:38652181 C>T maps to NM_006708.2 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr13:48947628 G>A did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr5:140431762 C>T maps to NM_013340.2 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chrX:39933374 C>T maps to NM_001123385.1 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr8:39624517 G>A maps to NM_001464.3 C452C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr17:3959635 T>C maps to NM_015113.3 Q1723Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr18:43685266 C>T maps to NM_138443.3 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr5:112889506 C>T maps to NM_022828.3 Q670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr17:39261741 C>T maps to NM_001146041.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr16:57738846 C>T maps to NM_032269.5 D253D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr14:21215867 A>G maps to NM_006683.4 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr6:144837471 T>C maps to NM_007124.2 N1784N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr19:11649777 C>T maps to NM_001299.4 Y12Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr9:138392970 T>A did not map to a codon.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr19:49517860 G>T did not map to a codon.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr5:139743378 C>T maps to ENST00000507527 D406D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr6:152265312 C>T maps to NM_001122741.1 R256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59X-01A-11D-A29Q-08 chr3:46713450 C>T maps to NM_147129.3 S869S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr19:55994209 G>A maps to NM_033113.2 T546T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr15:32460274 G>A maps to NM_001190455.1 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr6:45390462 G>A maps to ENST00000359524 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr5:126784894 C>T maps to NM_032446.2 G987G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr13:95858796 G>A maps to NM_005845.3 R384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr11:1025071 G>T maps to NM_005961.2 C999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Y-01A-11D-A26M-08 chr14:78174326 G>A maps to NM_006020.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr19:10464233 C>T maps to NM_003331.4 Q999Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr15:42456580 C>T maps to ENST00000348544 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr18:21663036 C>T maps to NM_001135993.1 R326*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr11:55541086 T>C maps to NM_001001967.1 H58H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr1:248801911 C>G maps to NM_001001827.1 V216V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr17:72862612 G>A maps to ENST00000442102 D159D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr16:66946576 G>A maps to NM_004062.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr8:17418004 G>A maps to NM_001164771.1 Q529Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr12:117685281 G>A maps to ENST00000338101 C932C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr2:238668783 A>G maps to NM_001137552.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr13:73396006 A>G maps to NM_006346.2 K231K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr15:48431346 C>A maps to NM_205850.2 I351I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr17:72340363 C>A maps to NM_153209.3 I153I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr19:40421658 G>A maps to NM_003890.2 C754C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr17:37619370 G>A did not map to a codon.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr5:179193304 C>T maps to NM_014757.4 Q432*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:197032023 A>G maps to NM_001994.2 C76C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr9:131600403 C>A maps to NM_004059.4 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr15:41192239 C>T maps to NM_020857.2 F408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr3:141011305 C>T maps to NM_001037172.1 H234H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:245852062 C>A maps to NM_018012.3 G1926G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr18:70209170 G>A maps to NM_182511.3 D75D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:151748666 C>T maps to NM_001083965.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr18:21110077 C>T maps to NM_013326.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:160784291 C>G maps to ENST00000263285 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr9:139391806 C>T maps to NM_017617.3 P2128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr6:143074326 A>G maps to NM_006734.3 L2420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr17:7842863 G>T maps to NM_001037144.4 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr19:18709694 G>A maps to NM_004750.4 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr10:72358720 G>A maps to NM_005041.4 N252N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:35884162 C>T maps to NM_005095.2 L1477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr13:33700313 G>A maps to NM_178007.2 G654G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr5:122700258 T>C maps to NM_153223.3 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr12:993362 C>T maps to NM_001184985.1 S1526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr8:85799875 G>T maps to NM_001100391.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr19:38160482 G>A maps to NM_152605.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:209785549 C>A maps to NM_020439.2 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr19:58370782 C>T maps to NM_032828.2 Q335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr1:206760349 T>C maps to ENST00000367118 Y390Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr2:21228378 G>A maps to NM_000384.2 P3787P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr4:70823023 G>A maps to NM_001891.2 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr8:52359717 C>A maps to NM_144651.4 G457G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr6:163899928 G>T did not map to a codon.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr14:105418649 G>A maps to NM_138420.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr19:5214706 G>A maps to NM_002850.3 D1453D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr19:17835964 T>G maps to NM_018174.4 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr17:42333043 G>T maps to NM_000342.3 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr3:119962485 C>T did not map to a codon.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr12:101505339 G>A did not map to a codon.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr5:102484975 C>T maps to ENST00000451606 R289*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A5A1-01A-11D-A29Q-08 chr14:105409472 G>T maps to NM_138420.2 A4105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr1:46527680 C>T maps to NM_001114172.1 E228E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr1:47755172 A>T maps to NM_001048166.1 C319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr16:56659783 C>T maps to ENST00000330439 C7C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr4:152048835 C>T maps to NM_001009555.3 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr1:157559033 G>A maps to NM_031282.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr6:39877612 C>A maps to ENST00000425303 G356G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr13:28608022 C>G did not map to a codon.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr12:19436439 C>T maps to ENST00000429027 Q514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6DY-01A-12D-A30X-08 chr8:2832108 G>A maps to NM_033225.5 A2868A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr19:51217084 G>A maps to ENST00000391814 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr17:39672160 G>A maps to NM_002275.3 I334I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr4:74351739 C>T maps to NM_001133.2 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr7:140285505 C>T maps to NM_015689.3 P376P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr12:32369194 C>G maps to NM_001714.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr1:183617688 A>T maps to NM_203454.2 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr8:67579178 C>A maps to NM_025054.4 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr2:141609266 C>T maps to NM_018557.2 A1555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr2:239353280 C>T maps to NM_001040445.1 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr22:40816927 G>C maps to NM_020831.3 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr11:26725365 T>C maps to NM_178498.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr2:20463105 A>C maps to ENST00000361078 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr19:4054987 G>A maps to NM_015898.2 S81S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr6:151687731 G>A maps to NM_020861.1 R157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E0-01A-11D-A30X-08 chr1:186064438 C>T maps to NM_031935.2 T3453T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr15:51975310 A>G maps to NM_013243.3 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr10:26377233 G>T maps to NM_017433.4 G488*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chrX:117775255 T>C maps to ENST00000276204 T1416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr3:47038460 C>A maps to NM_015175.1 I858I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr22:36680209 G>A maps to NM_002473.4 R1898R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr17:48678109 G>A maps to NM_018896.3 A1238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr12:51737622 G>A maps to NM_001971.5 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr3:123049809 C>T maps to NM_183357.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr1:247695156 G>A maps to NM_198074.4 Y219Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E1-01A-11D-A30X-08 chr14:25043657 C>A maps to NM_001911.2 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr12:70735907 G>T maps to NM_014515.5 A400A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr12:106838327 G>A maps to NM_018082.5 P681P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr8:53079445 C>G maps to NM_014682.2 S390S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr8:3141831 G>A maps to NM_033225.5 H1329H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chrX:70465272 G>A maps to ENST00000373988 R977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr19:49299744 G>A maps to NM_001190.3 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr2:27677276 G>A maps to NM_015662.1 F1158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr5:140627359 C>T maps to NM_018935.2 D738D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr8:85441792 C>G maps to NM_001100391.1 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr16:58149202 G>C maps to NM_013242.2 G145G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr1:117484586 C>T maps to NM_020440.2 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr2:68765197 C>T maps to NM_173545.2 G333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr10:125506293 G>A maps to NM_198148.2 R753*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr17:25950426 A>G did not map to a codon.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr16:4310114 C>T maps to NM_003223.2 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr12:56722257 G>A maps to NM_001127460.2 Y150Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr10:12129646 C>T maps to NM_018706.5 S212S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr19:15662135 G>T maps to NM_173483.3 E484*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr17:76496389 G>T maps to ENST00000389840 Y1865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E2-01A-11D-A30X-08 chr16:67199715 C>G maps to NM_001040667.2 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr11:33308013 T>C maps to NM_005734.3 S18S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr1:153958655 C>T maps to NM_002870.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr1:185939491 A>T maps to NM_031935.2 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr11:58979776 T>G maps to NM_001039396.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr15:75985563 G>A maps to NM_001897.4 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr20:48525009 T>G maps to NM_006038.3 S6S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr12:57112088 G>A maps to NM_001113203.1 S1075S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr5:131544973 A>G maps to NM_001142599.1 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr1:207818583 G>T maps to NM_175710.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr21:38511001 A>C maps to NM_003316.3 I549I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr11:111745900 A>G maps to NM_138378.1 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr12:50041124 G>T maps to NM_175736.4 R935R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr8:118169990 C>T maps to NM_173851.2 Y160Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr1:160099087 T>C maps to NM_000702.3 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr2:179393600 A>C maps to NM_133378.4 L33058*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr5:140229522 C>T maps to NM_031857.1 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr1:158618310 G>T maps to NM_003126.2 P1234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr3:127399140 G>A maps to NM_172027.2 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr10:122662579 G>T maps to NM_018117.11 E923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr1:12726652 C>T maps to NM_001013630.1 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr6:86329032 T>A maps to NM_006372.4 K371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr17:7680921 G>A maps to NM_020877.2 W1739*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr17:40822620 G>A maps to NM_024927.4 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr19:52723056 C>T maps to NM_014225.5 D414D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr4:85699757 G>A maps to NM_014991.4 I1472I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr8:28573785 G>A maps to NM_001440.2 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr2:176965062 G>A maps to NM_021193.3 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr5:154270985 G>C maps to NM_015465.3 L1359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E4-01A-11D-A30E-08 chr14:20389697 T>A maps to NM_001005483.1 I311I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr15:51696485 C>T maps to NM_181789.2 G397G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr12:77202834 G>A maps to NM_015336.2 S111S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr17:18874965 G>A maps to NM_001039999.2 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr3:99649663 G>C maps to NM_001042459.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr4:1834578 C>T maps to NM_012318.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr21:39755837 G>A maps to NM_001136154.1 G316G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E5-01A-11D-A30X-08 chr2:219735844 G>A maps to NM_006522.3 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr6:152539539 T>C did not map to a codon.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr18:9888098 T>G maps to NM_001098529.1 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr4:10447769 T>A maps to NM_053042.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr2:239090710 G>A maps to NM_030768.2 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr2:11053814 C>T maps to NM_002236.4 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr17:7222512 G>A maps to NM_032442.2 F1180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr4:26622237 T>C maps to NM_018317.2 F74F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chrX:78010845 T>C maps to NM_005296.2 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr20:16360453 G>A maps to NM_024704.4 D731D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr8:52321582 G>A maps to NM_144651.4 P867P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr1:43779602 G>T maps to NM_005424.2 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr12:49374246 C>T maps to NM_005430.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr9:131831377 G>A maps to NM_032809.2 S476S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr16:31473497 G>A maps to ENST00000408912 S305S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr1:55077405 C>T maps to NM_176782.2 T271T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr11:57367488 C>A maps to ENST00000403558 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr16:23417459 A>G maps to NM_153603.3 N533N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E6-01A-11D-A30X-08 chr19:39964092 G>A maps to NM_003169.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr7:141767224 C>T maps to ENST00000475668 R1668R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr19:36018835 G>A maps to NM_001166034.1 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr9:5920337 A>T maps to NM_001017969.2 P1886P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr17:80013938 G>A maps to NM_212492.1 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr17:26666642 C>A maps to NM_021137.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr12:85450802 C>T maps to NM_001079910.1 A744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr6:2770370 C>T maps to NM_020135.2 H344H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr1:111217281 C>T maps to NM_002232.3 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr13:25044067 G>A maps to NM_006437.3 F670F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E7-01A-11D-A31L-08 chr7:99909506 C>T maps to NM_001004351.4 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr1:186056761 C>T maps to NM_031935.2 H3116H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr11:40137467 G>A maps to NM_020929.1 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr19:44097044 G>A maps to NM_001007561.2 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr1:222805660 G>C maps to NM_198551.2 L1108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr20:58467115 G>A maps to NM_014258.2 Q765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr8:143784548 C>T maps to ENST00000292430 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr9:97522700 T>A maps to NM_001193329.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr1:208062819 G>A maps to NM_001025109.1 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr19:51172429 C>A maps to ENST00000391814 P937P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr19:43702386 A>G maps to NM_002780.3 N157N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr1:118479417 G>T maps to NM_006784.2 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr2:220285374 G>T maps to NM_001927.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A6E8-01A-11D-A31L-08 chr2:152698422 C>T maps to NM_000726.3 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr11:128844289 T>C maps to NM_001142685.1 S920S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr3:52304794 A>G maps to NM_025222.3 Y64Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr8:1900968 C>T maps to ENST00000398564 L1191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr11:5510454 T>C maps to NM_001005163.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr8:100866041 A>G maps to NM_017890.3 K3500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr2:69173529 C>G maps to NM_182536.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr7:55229297 C>T maps to NM_005228.3 C535C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr19:40540947 A>G maps to NM_001005851.2 F606F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr2:228846443 C>A maps to NM_001142644.1 E1698*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr1:155147950 C>T maps to NM_025058.3 N51N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr17:40323994 G>A maps to NM_012285.2 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr20:5904577 C>T maps to NM_001819.2 D596D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr8:103564149 C>T maps to NM_024410.3 C65C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr19:38633279 C>A maps to NM_015073.1 R1155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr9:21854676 G>A maps to NM_002451.3 K166K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr9:140809211 G>A maps to ENST00000277549 E243E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IL-01A-11D-A31L-08 chr9:37740870 C>G maps to NM_014907.2 G782G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr1:205768181 G>T maps to NM_173854.4 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr7:23556148 T>A did not map to a codon.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr4:89702351 T>C maps to NM_014883.2 K474K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr2:167289253 G>T maps to NM_002976.2 Y722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr8:32599589 G>T maps to ENST00000338921 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr5:40853135 C>T maps to NM_032587.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr20:44167962 G>A maps to ENST00000372665 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr2:60687904 G>A maps to NM_022893.3 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chrX:28807501 T>A maps to NM_014271.3 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr5:79933788 T>C maps to NM_000791.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr21:18924260 G>T maps to NM_001338.3 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr5:140201644 C>T maps to NM_018908.2 C95C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr17:3030695 A>T maps to ENST00000381953 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr22:41169987 T>C maps to NM_006358.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chrX:34149501 A>T maps to NM_203408.3 C298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr12:111954060 C>A maps to NM_002973.3 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr6:84140594 C>T did not map to a codon.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr17:65907563 C>T maps to ENST00000321892 D1314D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr21:38311177 T>C maps to NM_000411.5 E2E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr22:37263464 C>T maps to NM_013416.3 I101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr11:60658694 G>A maps to NM_014502.4 H486H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr17:18923108 C>T maps to NM_152351.3 C514C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr9:6504675 C>T maps to NM_152896.1 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr17:38182575 A>C maps to NM_014815.3 T606T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr2:73828484 C>T maps to NM_015120.4 D4011D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-QU-A6IO-01A-11D-A31L-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr9:130506866 C>T maps to NM_170600.2 R592R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr17:38933945 A>G maps to NM_181537.3 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr2:211438053 A>T maps to NM_001122633.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr1:228238396 C>T maps to ENST00000366753 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr20:43056984 C>T maps to ENST00000338692 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr9:133928257 C>T maps to ENST00000355048 D615D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr1:248569714 G>A maps to NM_030904.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr6:13592061 C>A maps to NM_012241.3 V137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr3:183521929 C>T maps to NM_018023.4 D1246D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr6:76373049 A>G maps to NM_015571.2 L270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr6:49986787 T>G maps to NM_001037497.1 R36R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IO-01A-11D-A31L-08 chr20:35383220 C>T maps to NM_001145315.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr6:63990359 G>A maps to NM_016571.2 R366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr6:33143389 C>T maps to NM_080680.2 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chrX:127185962 C>A maps to NM_138289.3 E75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chrX:102337985 G>A maps to NM_022052.1 Q213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr11:123886914 C>T maps to NM_001004462.1 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr12:11461247 C>T maps to NM_002723.3 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr15:34015066 C>T maps to NM_001036.3 D2257D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr19:14083866 G>A maps to NM_002918.4 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5748-01A-11D-1576-08 chr6:66205252 A>T maps to ENST00000370616 S17S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5761-01A-11D-1576-08 chr7:100350274 A>G maps to ENST00000349350 K849K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5762-01A-11D-1576-08 chr3:57488128 C>T maps to NM_178504.4 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CH-5766-01A-11D-1576-08 chr7:100348485 C>A maps to ENST00000349350 V496V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5495-01A-01D-1576-08 chr11:66314403 T>A did not map to a codon.
Sequencing variant TCGA-EJ-5498-01A-01D-1576-08 chr19:56090150 C>T maps to NM_152600.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-5505-01A-01D-1576-08 chr19:53960337 A>G did not map to a codon.
Sequencing variant TCGA-EJ-5511-01A-01D-1576-08 chr19:53950474 G>T did not map to a codon.
Sequencing variant TCGA-EJ-5542-01A-01D-1576-08 chr16:3613170 G>A maps to ENST00000448023 S636S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7331-01A-11D-2114-08 chr19:53958819 T>C maps to NM_001008401.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-7782-01A-11D-2114-08 chr8:43147833 C>G maps to NM_001005365.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr6:66115186 G>A maps to ENST00000370616 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EJ-8474-01A-11D-2395-08 chr16:1278551 A>T did not map to a codon.
Sequencing variant TCGA-EJ-A46G-01A-31D-A26M-08 chr13:39451252 G>T did not map to a codon.
Sequencing variant TCGA-EJ-A65F-01A-21D-A30X-08 chr11:13984531 G>C maps to NM_006108.2 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FC-A4JI-01A-11D-A257-08 chr19:43439763 G>A maps to NM_002783.2 D74D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G9-6373-01A-11D-1786-08 chr21:11047498 G>T did not map to a codon.
Sequencing variant TCGA-G9-6385-01A-11D-1786-08 chr21:11058352 T>C did not map to a codon.
Sequencing variant TCGA-G9-7523-01A-11D-2260-08 chr17:34641447 A>G did not map to a codon.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr21:11049591 C>T maps to NM_182482.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr21:11039297 C>T did not map to a codon.
Sequencing variant TCGA-HC-7738-01A-11D-2114-08 chr11:89392752 A>C did not map to a codon.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr21:11058352 T>C did not map to a codon.
Sequencing variant TCGA-HC-7750-01A-11D-2114-08 chr21:11038908 G>T did not map to a codon.
Sequencing variant TCGA-HC-7820-01A-11D-2114-08 chr1:19597013 G>T maps to NM_201252.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr11:89395332 A>G did not map to a codon.
Sequencing variant TCGA-HC-8256-01A-11D-2260-08 chr11:89395321 C>T did not map to a codon.
Sequencing variant TCGA-HC-8258-01A-11D-2260-08 chr21:11098838 C>T did not map to a codon.
Sequencing variant TCGA-HC-A6AQ-01A-11D-A30E-08 chr21:11038897 G>A did not map to a codon.
Sequencing variant TCGA-J4-A67M-01A-11D-A30E-08 chr21:11038953 T>C did not map to a codon.
Sequencing variant TCGA-J9-A52C-01A-11D-A26M-08 chr11:56143701 C>A maps to NM_001005204.1 A201A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KC-A4BN-01A-61D-A257-08 chr11:89395321 C>T did not map to a codon.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr18:61390554 G>A maps to NM_080475.2 A367A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59V-01A-11D-A29Q-08 chr19:4929358 C>T maps to ENST00000398240 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KK-A59Z-01A-12D-A26M-08 chr21:11058352 T>C did not map to a codon.
Sequencing variant TCGA-KK-A6E3-01A-21D-A30E-08 chr7:100363149 C>T maps to ENST00000349350 C1481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IM-01A-11D-A31L-08 chr6:132860432 G>A maps to NM_175057.3 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IN-01A-11D-A31L-08 chr1:247654713 C>T maps to NM_001004698.2 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-QU-A6IP-01A-11D-A31L-08 chr10:88769149 C>T maps to NM_133447.1 R381*. Only missense variants will be evaluated by CHASM.
