5112 NP_705833 G776S not found in SNVbox database
5252 NP_001070868 D61N not found in SNVbox database
5816 NP_001070868 R322Q not found in SNVbox database
6589 NP_705833 D323H not found in SNVbox database
8184 NP_705833 D488N not found in SNVbox database
8752 NP_001070868 C631Y not found in SNVbox database
8852 NP_705833 L260M not found in SNVbox database
8914 NP_705833 H290Y not found in SNVbox database
171 NP_705833 N975K not found in SNVbox database
415 NP_705833 Q644E not found in SNVbox database
703 NP_705833 E362Q not found in SNVbox database
767 NP_001070868 V565L not found in SNVbox database
824 NP_001070868 T263K not found in SNVbox database
969 NP_705833 W841C not found in SNVbox database
1005 NP_705833 W694R not found in SNVbox database
1166 NP_001070868 E654D not found in SNVbox database
1694 NP_001070868 E519K not found in SNVbox database
1988 NP_001070868 E21Q not found in SNVbox database
2165 NP_705833 F724L not found in SNVbox database
2469 NP_705833 V383I not found in SNVbox database
2477 NP_001070868 P770Q not found in SNVbox database
3411 NP_705833 L946F not found in SNVbox database
3589 NP_705833 S647C not found in SNVbox database
3791 NP_001070868 E656Q not found in SNVbox database
4308 NP_705833 F968L not found in SNVbox database
4370 NP_001070868 D85H not found in SNVbox database
4394 NP_001070868 R640H not found in SNVbox database
4616 NP_001070868 H676D not found in SNVbox database
4971 NP_705833 S789F not found in SNVbox database
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:1572103 C>T maps to ENST00000401097 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:1572103 C>T maps to ENST00000401097 L617L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:7863154 G>A maps to ENST00000377532 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:7863154 G>A maps to ENST00000377532 S307S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:55464879 C>T maps to NM_057176.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:55464879 C>T maps to NM_057176.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:203134454 C>T maps to NM_001048230.1 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:203134454 C>T maps to NM_001048230.1 F136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:203472793 C>G maps to NM_014359.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:203472793 C>G maps to NM_014359.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:213032276 C>T maps to NM_014053.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:213032276 C>T maps to NM_014053.2 I161I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:236973893 C>T maps to NM_000254.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr1:236973893 C>T maps to NM_000254.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr10:27447545 G>A maps to NM_001172303.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr10:27447545 G>A maps to NM_001172303.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr10:89717614 C>T maps to NM_000314.4 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr10:89717614 C>T maps to NM_000314.4 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr10:105201704 G>A maps to NM_014976.1 E1560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr10:105201704 G>A maps to NM_014976.1 E1560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr11:104866482 A>G maps to NM_001136112.1 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr11:104866482 A>G maps to NM_001136112.1 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr11:117109496 A>C maps to NM_207343.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr11:117109496 A>C maps to NM_207343.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr11:134253723 G>A maps to NM_054025.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr11:134253723 G>A maps to NM_054025.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr12:55863490 G>A maps to NM_001005499.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr12:55863490 G>A maps to NM_001005499.1 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr12:57550034 C>T maps to NM_002332.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr12:57550034 C>T maps to NM_002332.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr13:78176202 C>T maps to NM_144777.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr13:78176202 C>T maps to NM_144777.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr14:74534263 C>T maps to NM_005589.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr14:74534263 C>T maps to NM_005589.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr15:43663590 T>C maps to ENST00000399460 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr15:43663590 T>C maps to ENST00000399460 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr16:2106736 C>T maps to NM_000548.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr16:2106736 C>T maps to NM_000548.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr16:17232373 C>T maps to NM_022166.3 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr16:17232373 C>T maps to NM_022166.3 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr16:66670349 G>A maps to NM_178818.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr16:66670349 G>A maps to NM_178818.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:6553726 G>A maps to NM_016060.2 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:6553726 G>A maps to NM_016060.2 Q19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:7752017 C>G maps to NM_001080424.1 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:7752017 C>G maps to NM_001080424.1 L804L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:30815054 C>A maps to NM_003885.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:30815054 C>A maps to NM_003885.2 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:38556816 A>G maps to ENST00000357601 I957I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:38556816 A>G maps to ENST00000357601 I957I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:41956723 G>A maps to NM_005374.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:41956723 G>A maps to NM_005374.3 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:46030366 C>T maps to NM_024320.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr17:46030366 C>T maps to NM_024320.2 E78E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr18:580566 G>A maps to NM_004066.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr18:580566 G>A maps to NM_004066.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr18:21529760 G>C maps to ENST00000416669 L3130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr18:21529760 G>C maps to ENST00000416669 L3130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr18:60017105 G>A maps to NM_003839.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr18:60017105 G>A maps to NM_003839.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:12800191 G>C maps to ENST00000380339 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:12800191 G>C maps to ENST00000380339 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:36381328 G>A maps to ENST00000352614 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:36381328 G>A maps to ENST00000352614 Q376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:39965348 C>T maps to NM_003169.3 R1005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:39965348 C>T maps to NM_003169.3 R1005R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:55263155 C>T maps to NM_015868.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr19:55263155 C>T maps to NM_015868.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:24247078 C>A maps to ENST00000338315 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:24247078 C>A maps to ENST00000338315 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:48950792 C>T maps to NM_000233.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:48950792 C>T maps to NM_000233.3 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:73145355 C>T maps to NM_004097.2 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:73145355 C>T maps to NM_004097.2 H125H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:101646212 G>A maps to NM_001102426.1 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:101646212 G>A maps to NM_001102426.1 F639F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:197085611 C>T maps to NM_020760.1 K1400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr2:197085611 C>T maps to NM_020760.1 K1400K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr20:60511901 C>T maps to NM_001794.2 N884N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr20:60511901 C>T maps to NM_001794.2 N884N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr3:56667587 A>G maps to ENST00000447900 F1077F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr3:56667587 A>G maps to ENST00000447900 F1077F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr3:100963076 G>A maps to NM_016247.2 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr3:100963076 G>A maps to NM_016247.2 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr3:112993327 G>A maps to ENST00000273395 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr3:112993327 G>A maps to ENST00000273395 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr3:137800603 G>A maps to NM_173543.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr3:137800603 G>A maps to NM_173543.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr5:236601 G>A maps to NM_004168.2 E440E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr5:236601 G>A maps to NM_004168.2 E440E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr5:480052 G>A maps to NM_004174.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr5:480052 G>A maps to NM_004174.2 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr5:9197363 C>T maps to NM_003966.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr5:9197363 C>T maps to NM_003966.2 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr6:15496964 G>A maps to NM_004973.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr6:15496964 G>A maps to NM_004973.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr6:32135383 C>T maps to NM_030652.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr6:32135383 C>T maps to NM_030652.2 I262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr7:1525078 G>T maps to ENST00000389470 G1168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr7:1525078 G>T maps to ENST00000389470 G1168G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr7:97949381 C>G maps to NM_018842.4 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr7:97949381 C>G maps to NM_018842.4 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr7:120373013 G>A maps to NM_012281.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr7:120373013 G>A maps to NM_012281.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr7:157926523 G>A maps to NM_002847.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr7:157926523 G>A maps to NM_002847.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr9:79328480 G>A maps to NM_015225.2 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr9:79328480 G>A maps to NM_015225.2 Q305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr9:135145013 C>T maps to ENST00000372169 L2425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chr9:135145013 C>T maps to ENST00000372169 L2425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chrX:53561047 G>A maps to ENST00000276009 L4316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chrX:53561047 G>A maps to ENST00000276009 L4316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chrX:77373592 G>A maps to NM_000291.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chrX:77373592 G>A maps to NM_000291.3 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chrX:153941666 G>A maps to NM_001081573.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VR-01A-11D-A10S-08 chrX:153941666 G>A maps to NM_001081573.1 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:43894131 C>T maps to NM_015284.2 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:43894131 C>T maps to NM_015284.2 R482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:147121992 G>A maps to NM_016361.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:147121992 G>A maps to NM_016361.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:152080238 G>A maps to NM_007113.2 D1818D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:152080238 G>A maps to NM_007113.2 D1818D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:203672792 C>T maps to NM_001001396.1 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:203672792 C>T maps to NM_001001396.1 D317D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:246927546 G>A did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr1:246927546 G>A did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr10:93875 G>A maps to NM_177987.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr10:93875 G>A maps to NM_177987.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr10:25464454 C>T maps to NM_020752.2 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr10:25464454 C>T maps to NM_020752.2 R36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr11:800181 C>T maps to NM_145886.3 Q741Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr11:800181 C>T maps to NM_145886.3 Q741Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr11:88911390 G>A maps to NM_000372.4 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr11:88911390 G>A maps to NM_000372.4 Q90Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr11:113848496 G>A maps to NM_213621.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr11:113848496 G>A maps to NM_213621.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr11:115047274 G>A maps to NM_014333.3 D416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr11:115047274 G>A maps to NM_014333.3 D416D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:333193 G>A maps to NM_016615.3 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:333193 G>A maps to NM_016615.3 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:26208356 C>T maps to NM_001164747.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:26208356 C>T maps to NM_001164747.1 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:26208362 C>T maps to NM_001164747.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:26208362 C>T maps to NM_001164747.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:41337929 C>T maps to NM_001843.2 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:41337929 C>T maps to NM_001843.2 I547I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:81112733 C>T maps to NM_005593.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr12:81112733 C>T maps to NM_005593.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr13:101257340 G>A maps to NM_032813.2 I730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr13:101257340 G>A maps to NM_032813.2 I730I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr15:35274378 C>T maps to NM_014106.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr15:35274378 C>T maps to NM_014106.3 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr16:3140072 G>A maps to NM_032805.1 H399H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr16:3140072 G>A maps to NM_032805.1 H399H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr16:4385081 C>T maps to NM_032575.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr16:4385081 C>T maps to NM_032575.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr17:35830525 C>G maps to NM_001166105.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr17:35830525 C>G maps to NM_001166105.1 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr17:71282207 C>T maps to NM_012121.4 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr17:71282207 C>T maps to NM_012121.4 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr18:9570272 T>C maps to NM_001042388.1 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr18:9570272 T>C maps to NM_001042388.1 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr18:66344337 G>A maps to NM_019022.3 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr18:66344337 G>A maps to NM_019022.3 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr19:3589525 T>G maps to NM_133261.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr19:3589525 T>G maps to NM_133261.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr19:7619549 C>T maps to NM_001166111.1 R869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr19:7619549 C>T maps to NM_001166111.1 R869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr19:8161807 C>T maps to NM_032447.3 K1790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr19:8161807 C>T maps to NM_032447.3 K1790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr19:55889063 C>T maps to NM_139172.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr19:55889063 C>T maps to NM_139172.1 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr2:28635080 C>T maps to NM_005253.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr2:28635080 C>T maps to NM_005253.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr2:152476024 G>A maps to NM_001164507.1 I3604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr2:152476024 G>A maps to NM_001164507.1 I3604I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr2:158412761 C>G maps to NM_145259.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr2:158412761 C>G maps to NM_145259.2 A129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr20:62199859 C>T maps to NM_001037335.2 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr20:62199859 C>T maps to NM_001037335.2 A527A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr22:29660193 C>T maps to NM_012265.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr22:29660193 C>T maps to NM_012265.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr3:11372812 G>A did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr3:11372812 G>A did not map to a codon.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr3:78734953 G>A maps to NM_002941.3 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr3:78734953 G>A maps to NM_002941.3 C428C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr3:108195276 G>A maps to NM_014981.1 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr3:108195276 G>A maps to NM_014981.1 N420N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr3:148789137 T>C maps to NM_003071.3 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr3:148789137 T>C maps to NM_003071.3 E265E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:6615954 G>A maps to NM_015274.1 P858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:6615954 G>A maps to NM_015274.1 P858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:39246133 C>T maps to NM_025132.3 Y869Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:39246133 C>T maps to NM_025132.3 Y869Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:40752790 G>C maps to NM_024677.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:40752790 G>C maps to NM_024677.4 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:89326035 T>C maps to NM_017912.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:89326035 T>C maps to NM_017912.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:157688962 G>A maps to NM_016205.2 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:157688962 G>A maps to NM_016205.2 Q295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:175896931 C>T maps to NM_014269.4 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr4:175896931 C>T maps to NM_014269.4 Q86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr5:6742640 G>T maps to NM_006999.4 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr5:6742640 G>T maps to NM_006999.4 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr5:80554978 G>A maps to NM_001825.2 W307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr5:80554978 G>A maps to NM_001825.2 W307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr5:140741883 C>T maps to NM_018923.2 Q728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr5:140741883 C>T maps to NM_018923.2 Q728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr6:29395166 C>T maps to NM_013937.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr6:29395166 C>T maps to NM_013937.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr6:64422275 C>T maps to NM_015153.2 Q1598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr6:64422275 C>T maps to NM_015153.2 Q1598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr7:101844946 C>T maps to ENST00000360264 D801D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr7:101844946 C>T maps to ENST00000360264 D801D. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BI-A0VS-01A-11D-A10S-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr7:151970951 G>A maps to ENST00000355193 R284*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BI-A0VS-01A-11D-A10S-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr7:151970951 G>A maps to ENST00000355193 R284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr8:10480213 C>T maps to NM_178857.5 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr8:10480213 C>T maps to NM_178857.5 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr8:100155379 C>T maps to NM_017890.3 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr8:100155379 C>T maps to NM_017890.3 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr9:134362660 C>T maps to NM_013318.3 F1988F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chr9:134362660 C>T maps to NM_013318.3 F1988F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chrX:135291483 C>T maps to NM_001159702.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chrX:135291483 C>T maps to NM_001159702.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chrX:155003761 C>T maps to NM_005840.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chrX:155003761 C>T maps to NM_005840.1 Q77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chrX:155239719 G>A maps to NM_002186.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A0VS-01A-11D-A10S-08 chrX:155239719 G>A maps to NM_002186.2 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr10:91469149 C>T maps to ENST00000416354 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr10:91469149 C>T maps to ENST00000416354 Q95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr11:59245561 C>A maps to NM_001004705.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr11:59245561 C>A maps to NM_001004705.1 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr11:59949161 C>T maps to NM_152852.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr11:59949161 C>T maps to NM_152852.1 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr17:34067537 G>A maps to NM_033315.3 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr17:34067537 G>A maps to NM_033315.3 Q109Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr18:43532368 G>A maps to NM_020964.2 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr18:43532368 G>A maps to NM_020964.2 R417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr20:9546626 G>A maps to NM_177990.2 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr20:9546626 G>A maps to NM_177990.2 I465I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr20:62192593 G>A maps to NM_001037335.2 F2329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr20:62192593 G>A maps to NM_001037335.2 F2329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr3:100962777 T>A maps to NM_016247.2 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr3:100962777 T>A maps to NM_016247.2 A799A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr3:123044255 G>A maps to NM_183357.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr3:123044255 G>A maps to NM_183357.2 I667I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr4:46066530 A>T maps to NM_173536.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr4:46066530 A>T maps to NM_173536.3 I184I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr4:122853995 G>A maps to NM_001130698.1 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr4:122853995 G>A maps to NM_001130698.1 N139N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr5:140167431 A>G maps to NM_018900.2 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr5:140167431 A>G maps to NM_018900.2 A519A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr5:140167440 C>G maps to NM_018900.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr5:140167440 C>G maps to NM_018900.2 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr5:140167458 G>A maps to NM_018900.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr5:140167458 G>A maps to NM_018900.2 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr5:140167467 G>A maps to NM_018900.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr5:140167467 G>A maps to NM_018900.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr6:12121869 C>T maps to NM_002114.2 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr6:12121869 C>T maps to NM_002114.2 S614S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr8:24181360 C>T maps to NM_014265.4 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr8:24181360 C>T maps to NM_014265.4 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr9:990869 C>T maps to NM_021240.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chr9:990869 C>T maps to NM_021240.2 R428R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chrX:2406945 C>A maps to NM_004729.3 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chrX:2406945 C>A maps to NM_004729.3 L605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chrX:14027220 G>T maps to NM_017856.2 C180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chrX:14027220 G>T maps to NM_017856.2 C180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chrX:37663317 A>T maps to NM_000397.3 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BI-A20A-01A-11D-A14W-08 chrX:37663317 A>T maps to NM_000397.3 T362T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr1:145367738 A>G maps to NM_001039703.4 K3445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr1:145367738 A>G maps to NM_001039703.4 K3445K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr12:109537061 C>T maps to NM_080911.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr12:109537061 C>T maps to NM_080911.2 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr7:42949704 T>C maps to NM_001099858.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr7:42949704 T>C maps to NM_001099858.1 G323G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chrX:76814317 C>T did not map to a codon.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chrX:76814317 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr1:72400956 G>A maps to NM_173808.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr1:72400956 G>A maps to NM_173808.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr1:169798415 C>T maps to NM_018186.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr1:169798415 C>T maps to NM_018186.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr13:108861174 T>A maps to NM_001098268.1 R814R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr13:108861174 T>A maps to NM_001098268.1 R814R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr14:50100350 G>T maps to NM_018139.2 S506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr14:50100350 G>T maps to NM_018139.2 S506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr14:59112963 G>A maps to NM_016651.5 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr14:59112963 G>A maps to NM_016651.5 K541K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr14:96998946 C>G maps to NM_032632.3 S266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr14:96998946 C>G maps to NM_032632.3 S266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr15:22990122 C>T maps to NM_014608.2 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr15:22990122 C>T maps to NM_014608.2 Q915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr16:46943726 C>T maps to NM_133443.2 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr16:46943726 C>T maps to NM_133443.2 D236D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr17:48559579 G>A maps to NM_018346.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr17:48559579 G>A maps to NM_018346.1 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr17:73738774 C>T maps to NM_001005619.1 I965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr17:73738774 C>T maps to NM_001005619.1 I965I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr19:36499192 C>A maps to ENST00000455847 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr19:36499192 C>A maps to ENST00000455847 E247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr2:163002165 G>A maps to ENST00000233604 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr2:163002165 G>A maps to ENST00000233604 H95H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr20:33539595 C>T maps to NM_000178.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr20:33539595 C>T maps to NM_000178.2 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr20:57598815 C>T maps to NM_030773.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr20:57598815 C>T maps to NM_030773.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr21:28210810 G>A maps to NM_006988.3 C717C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr21:28210810 G>A maps to NM_006988.3 C717C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr22:29534801 T>G maps to NM_032045.4 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr22:29534801 T>G maps to NM_032045.4 A385A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr3:89390120 C>T maps to NM_005233.5 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr3:89390120 C>T maps to NM_005233.5 C290C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr3:195515363 G>A maps to NM_018406.5 D1029D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr3:195515363 G>A maps to NM_018406.5 D1029D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr4:4436544 C>T maps to NM_016930.2 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr4:4436544 C>T maps to NM_016930.2 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr4:149356644 C>T maps to ENST00000511528 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr4:149356644 C>T maps to ENST00000511528 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr4:184367412 G>C maps to NM_017632.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr4:184367412 G>C maps to NM_017632.2 R192R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr5:231089 A>C maps to NM_004168.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr5:231089 A>C maps to NM_004168.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr5:115351378 A>C maps to NM_173800.4 I891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr5:115351378 A>C maps to NM_173800.4 I891I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr6:25826751 C>T maps to NM_005074.3 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr6:25826751 C>T maps to NM_005074.3 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr6:36979600 C>T maps to NM_173558.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr6:36979600 C>T maps to NM_173558.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr6:45909282 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr6:45909282 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr8:41563759 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr8:41563759 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr8:56436428 C>T maps to NM_052898.1 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr8:56436428 C>T maps to NM_052898.1 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr8:70964458 A>T maps to NM_024504.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chr8:70964458 A>T maps to NM_024504.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chrX:108673541 G>A maps to ENST00000218006 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chrX:108673541 G>A maps to ENST00000218006 F595F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chrX:118222150 C>G maps to NM_020721.1 V1014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chrX:118222150 C>G maps to NM_020721.1 V1014V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chrX:129769011 T>C maps to NM_182314.1 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chrX:129769011 T>C maps to NM_182314.1 K484K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chrX:153217995 C>T maps to ENST00000369984 A1681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BE-01B-11D-A13W-08 chrX:153217995 C>T maps to ENST00000369984 A1681A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:156534462 C>T maps to NM_178229.4 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:156534462 C>T maps to NM_178229.4 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:230486820 C>T maps to ENST00000321327 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr1:230486820 C>T maps to ENST00000321327 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr10:101090616 C>T maps to NM_020348.2 D491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr10:101090616 C>T maps to NM_020348.2 D491D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:17426063 C>T maps to ENST00000302539 A1185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:17426063 C>T maps to ENST00000302539 A1185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:111635534 A>G maps to NM_181699.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:111635534 A>G maps to NM_181699.2 C100C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:111795060 C>G maps to NM_080659.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr11:111795060 C>G maps to NM_080659.2 S15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr12:51887507 C>G maps to NM_001039960.1 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr12:51887507 C>G maps to NM_001039960.1 L907L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr12:120650347 G>A maps to NM_001080855.1 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr12:120650347 G>A maps to NM_001080855.1 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr12:122690992 C>T maps to NM_030765.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr12:122690992 C>T maps to NM_030765.2 F65F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr12:122691460 C>A maps to NM_030765.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr12:122691460 C>A maps to NM_030765.2 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr14:68265154 C>T maps to NM_015346.3 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr14:68265154 C>T maps to NM_015346.3 K608K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr15:58830667 C>T maps to NM_000236.2 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr15:58830667 C>T maps to NM_000236.2 C75C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:20996704 G>A maps to NM_017539.1 Y2453Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:20996704 G>A maps to NM_017539.1 Y2453Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:22343427 C>G maps to NM_018119.2 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:22343427 C>G maps to NM_018119.2 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:30768369 A>C maps to NM_000294.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:30768369 A>C maps to NM_000294.2 G391G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:31382736 C>T maps to NM_000887.3 Q642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr16:31382736 C>T maps to NM_000887.3 Q642*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1BF-01B-11D-A13W-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-C5-A1BF-01B-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr17:5485359 G>A maps to NM_033004.3 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr17:5485359 G>A maps to NM_033004.3 Y157Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr18:28742591 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr18:28742591 G>T did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr19:1008187 C>T maps to NM_138690.1 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr19:1008187 C>T maps to NM_138690.1 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr19:58385761 C>G maps to NM_001144989.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr19:58385761 C>G maps to NM_001144989.1 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr2:105954073 C>T maps to NM_024093.1 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr2:105954073 C>T maps to NM_024093.1 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr2:152586146 G>A maps to NM_001164507.1 Y20Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr2:152586146 G>A maps to NM_001164507.1 Y20Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr20:25450667 C>T maps to NM_025176.4 R1104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr20:25450667 C>T maps to NM_025176.4 R1104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr20:42162660 T>C maps to NM_032107.4 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr20:42162660 T>C maps to NM_032107.4 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr21:27070995 A>C maps to NM_021219.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr21:27070995 A>C maps to NM_021219.2 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr3:31725291 A>G maps to NM_017784.4 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr3:31725291 A>G maps to NM_017784.4 P520P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr3:49160389 G>C maps to NM_002292.3 L1440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr3:49160389 G>C maps to NM_002292.3 L1440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr3:140407215 C>T maps to NM_152616.4 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr3:140407215 C>T maps to NM_152616.4 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr4:66189875 G>A maps to NM_004439.5 Q1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr4:66189875 G>A maps to NM_004439.5 Q1024*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr4:146059409 C>T maps to ENST00000447906 Q839Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr4:146059409 C>T maps to ENST00000447906 Q839Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr4:187629359 G>C maps to ENST00000260147 S541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr4:187629359 G>C maps to ENST00000260147 S541*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr5:74677812 C>T maps to NM_001130105.1 W654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr5:74677812 C>T maps to NM_001130105.1 W654*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr5:118866972 C>T maps to NM_000414.3 Q623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr5:118866972 C>T maps to NM_000414.3 Q623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr5:140228211 C>T maps to NM_031857.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr5:140228211 C>T maps to NM_031857.1 F44F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr7:73097114 G>A maps to NM_032317.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr7:73097114 G>A maps to NM_032317.2 F213F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr7:143039070 G>T maps to NM_000083.2 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chr7:143039070 G>T maps to NM_000083.2 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chrX:53658566 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BF-01B-11D-A13W-08 chrX:53658566 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:6680011 C>G maps to NM_153812.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:6680011 C>G maps to NM_153812.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:92184976 G>A maps to NM_003243.4 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:92184976 G>A maps to NM_003243.4 T486T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:109740253 C>T maps to NM_020775.3 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:109740253 C>T maps to NM_020775.3 V760V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:145532811 C>T maps to NM_003637.3 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:145532811 C>T maps to NM_003637.3 F377F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:158369019 G>A maps to NM_001004475.1 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:158369019 G>A maps to NM_001004475.1 I79I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:179989082 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr1:179989082 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr10:50819079 G>A maps to NM_003055.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr10:50819079 G>A maps to NM_003055.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr10:100374768 C>T maps to NM_021828.4 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr10:100374768 C>T maps to NM_021828.4 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:3716726 G>A maps to NM_016320.4 F1373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:3716726 G>A maps to NM_016320.4 F1373F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:12316099 C>T maps to NM_032867.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:12316099 C>T maps to NM_032867.2 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:61300490 G>A maps to NM_004200.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:61300490 G>A maps to NM_004200.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:111572231 G>A maps to NM_015191.1 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:111572231 G>A maps to NM_015191.1 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:117163787 C>G maps to NM_012104.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr11:117163787 C>G maps to NM_012104.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:6710827 G>A maps to ENST00000309577 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:6710827 G>A maps to ENST00000309577 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:7945645 C>T maps to NM_024865.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:7945645 C>T maps to NM_024865.2 V84V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:56092523 G>C maps to ENST00000347027 S367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:56092523 G>C maps to ENST00000347027 S367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:118615107 C>T maps to NM_016281.3 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr12:118615107 C>T maps to NM_016281.3 K531K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr14:61446333 G>A maps to NM_020810.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr14:61446333 G>A maps to NM_020810.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr14:94088399 G>T maps to ENST00000393153 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr14:94088399 G>T maps to ENST00000393153 L1629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr15:73615838 G>A maps to NM_005477.2 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr15:73615838 G>A maps to NM_005477.2 F865F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr15:86189139 C>G maps to NM_006738.4 L1443L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr15:86189139 C>G maps to NM_006738.4 L1443L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1BI-01B-11D-A13W-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-C5-A1BI-01B-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr16:89985854 C>T maps to ENST00000304984 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr16:89985854 C>T maps to ENST00000304984 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr17:1639341 C>T maps to NM_001163809.1 R1779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr17:1639341 C>T maps to NM_001163809.1 R1779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr17:72767863 C>T maps to NM_015654.3 *208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr17:72767863 C>T maps to NM_015654.3 *208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:6901985 C>T maps to ENST00000381407 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:6901985 C>T maps to ENST00000381407 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:18378220 G>C maps to NM_001145304.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:18378220 G>C maps to NM_001145304.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:32954773 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:32954773 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:33502622 G>A maps to NM_033103.4 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:33502622 G>A maps to NM_033103.4 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:36271141 C>T maps to ENST00000007510 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:36271141 C>T maps to ENST00000007510 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:41759595 G>C maps to NM_021913.3 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:41759595 G>C maps to NM_021913.3 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:58233777 G>A maps to ENST00000335820 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr19:58233777 G>A maps to ENST00000335820 V98V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr2:44079963 C>T maps to NM_022437.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr2:44079963 C>T maps to NM_022437.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr2:130953800 G>A maps to NM_207312.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr2:130953800 G>A maps to NM_207312.2 F49F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr2:179614187 C>T maps to ENST00000375038 E4315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr2:179614187 C>T maps to ENST00000375038 E4315E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr20:13899728 G>A maps to NM_025229.1 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr20:13899728 G>A maps to NM_025229.1 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr20:30746295 C>T maps to NM_014742.3 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr20:30746295 C>T maps to NM_014742.3 I516I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr22:42483074 G>A maps to NM_002490.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr22:42483074 G>A maps to NM_002490.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr4:90169398 C>T maps to NM_198281.2 K621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr4:90169398 C>T maps to NM_198281.2 K621K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:56209779 C>T maps to NM_153706.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:56209779 C>T maps to NM_153706.3 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:102262313 G>A maps to NM_000919.3 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:102262313 G>A maps to NM_000919.3 E156E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:135391394 C>T maps to NM_000358.2 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:135391394 C>T maps to NM_000358.2 I479I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:140532129 C>T maps to NM_018939.2 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:140532129 C>T maps to NM_018939.2 F764F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:173376972 C>T maps to NM_030627.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr5:173376972 C>T maps to NM_030627.2 F519F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:27798994 C>G maps to NM_003541.2 *104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:27798994 C>G maps to NM_003541.2 *104S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:31868749 C>T maps to NM_181842.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:31868749 C>T maps to NM_181842.2 Q111Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:75975014 G>A maps to NM_018247.3 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:75975014 G>A maps to NM_018247.3 Q129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:159457434 C>T maps to NM_054114.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr6:159457434 C>T maps to NM_054114.3 P540P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr7:100677707 C>G maps to NM_001040105.1 S1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr7:100677707 C>G maps to NM_001040105.1 S1004*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr8:95188868 A>C maps to NM_001144663.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr8:95188868 A>C maps to NM_001144663.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr9:79840895 G>T maps to ENST00000376646 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chr9:79840895 G>T maps to ENST00000376646 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chrX:68383009 C>T maps to NM_145119.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BI-01B-11D-A13W-08 chrX:68383009 C>T maps to NM_145119.3 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:155450753 G>C maps to ENST00000368346 S636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:155450753 G>C maps to ENST00000368346 S636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:155796640 G>A maps to ENST00000368331 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:155796640 G>A maps to ENST00000368331 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:200571166 G>C maps to NM_014875.2 S670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:200571166 G>C maps to NM_014875.2 S670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:205589547 G>C maps to NM_001973.2 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:205589547 G>C maps to NM_001973.2 S209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:248685273 G>A maps to NM_001013355.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr1:248685273 G>A maps to NM_001013355.1 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr10:24909043 G>A maps to NM_020824.3 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr10:24909043 G>A maps to NM_020824.3 Q594*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr10:119026277 C>T maps to NM_003054.4 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr10:119026277 C>T maps to NM_003054.4 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr10:124377809 C>G maps to ENST00000368915 L1723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr10:124377809 C>G maps to ENST00000368915 L1723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr11:9444573 C>T maps to NM_006391.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr11:9444573 C>T maps to NM_006391.2 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr11:102563729 C>T maps to NM_022122.2 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr11:102563729 C>T maps to NM_022122.2 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr12:52180552 G>A maps to NM_014191.2 K1390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr12:52180552 G>A maps to NM_014191.2 K1390K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr12:125298774 G>A maps to NM_005505.4 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr12:125298774 G>A maps to NM_005505.4 F201F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr14:24801113 G>A maps to NM_139247.3 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr14:24801113 G>A maps to NM_139247.3 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr14:69256774 G>A maps to NM_004926.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr14:69256774 G>A maps to NM_004926.2 I164I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr15:82512458 C>T maps to NM_024580.5 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr15:82512458 C>T maps to NM_024580.5 G468G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr15:84683324 G>A maps to NM_207517.2 K1335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr15:84683324 G>A maps to NM_207517.2 K1335K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr15:90904046 C>T maps to NM_001004309.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr15:90904046 C>T maps to NM_001004309.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr15:90904151 C>T maps to NM_001004309.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr15:90904151 C>T maps to NM_001004309.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr16:3274469 G>A maps to NM_198088.2 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr16:3274469 G>A maps to NM_198088.2 R204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr16:31282367 C>G maps to NM_001145808.1 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr16:31282367 C>G maps to NM_001145808.1 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:1437391 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:1437391 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:7318955 C>G maps to NM_020795.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:7318955 C>G maps to NM_020795.2 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:8109912 C>T maps to NM_004217.2 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:8109912 C>T maps to NM_004217.2 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:37566918 G>A maps to NM_004774.3 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr17:37566918 G>A maps to NM_004774.3 Q519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr19:7593568 C>T maps to NM_020533.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr19:7593568 C>T maps to NM_020533.2 R322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr19:12874589 G>C maps to NM_013312.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr19:12874589 G>C maps to NM_013312.2 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:27892131 C>G maps to NM_018158.2 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:27892131 C>G maps to NM_018158.2 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:121107167 C>G maps to NM_002193.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:121107167 C>G maps to NM_002193.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:191552002 G>C maps to NM_005966.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:191552002 G>C maps to NM_005966.3 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:232952240 T>C maps to NM_152383.4 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr2:232952240 T>C maps to NM_152383.4 Y137Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr20:2411090 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr20:2411090 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr20:37357038 C>G maps to NM_080552.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr20:37357038 C>G maps to NM_080552.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr20:47592586 T>C maps to NM_006420.2 D603D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr20:47592586 T>C maps to NM_006420.2 D603D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr20:48252849 C>G maps to NM_004776.3 *389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr20:48252849 C>G maps to NM_004776.3 *389S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr21:33887493 C>T maps to NM_058187.3 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr21:33887493 C>T maps to NM_058187.3 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr22:24219355 C>G maps to NM_030807.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr22:24219355 C>G maps to NM_030807.3 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr22:25007113 C>T maps to NM_005265.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr22:25007113 C>T maps to NM_005265.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:40192619 G>A maps to NM_015460.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:40192619 G>A maps to NM_015460.2 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:52003447 G>A maps to NM_032750.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:52003447 G>A maps to NM_032750.2 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:121410566 C>G maps to ENST00000393667 V2548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:121410566 C>G maps to ENST00000393667 V2548V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:138668372 C>T maps to NM_001040061.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr3:138668372 C>T maps to NM_001040061.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr4:7056572 C>G maps to NM_152293.2 S352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr4:7056572 C>G maps to NM_152293.2 S352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr4:57182676 G>A maps to NM_020722.1 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr4:57182676 G>A maps to NM_020722.1 P1003P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr5:140221088 G>A maps to NM_018911.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr5:140221088 G>A maps to NM_018911.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr5:149215949 C>G maps to NM_133263.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr5:149215949 C>G maps to NM_133263.3 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr6:11213695 G>A maps to NM_006403.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr6:11213695 G>A maps to NM_006403.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:64438700 G>C maps to NM_015852.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:64438700 G>C maps to NM_015852.3 L416L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:101988930 G>A maps to NM_001146210.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:101988930 G>A maps to NM_001146210.1 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:128414647 G>A maps to NM_001708.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:128414647 G>A maps to NM_001708.2 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:158445170 C>T maps to NM_017760.5 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr7:158445170 C>T maps to NM_017760.5 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr8:40532226 C>T maps to NM_024645.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr8:40532226 C>T maps to NM_024645.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr8:93004061 G>A maps to NM_175634.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr8:93004061 G>A maps to NM_175634.2 R266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:21187089 G>A maps to NM_021068.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:21187089 G>A maps to NM_021068.2 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:34993235 A>G maps to NM_001135005.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:34993235 A>G maps to NM_001135005.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:113562807 C>G maps to ENST00000189978 S723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:113562807 C>G maps to ENST00000189978 S723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:125023708 C>T maps to NM_033117.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:125023708 C>T maps to NM_033117.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:130207190 C>T maps to NM_007135.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:130207190 C>T maps to NM_007135.2 L404L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:131271284 C>G maps to NM_001003722.1 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:131271284 C>G maps to NM_001003722.1 S77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:136523567 G>A maps to NM_000787.3 *618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chr9:136523567 G>A maps to NM_000787.3 *618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chrX:47101545 C>T maps to NM_004651.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BJ-01A-11D-A13W-08 chrX:47101545 C>T maps to NM_004651.3 F458F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:1650894 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:1650894 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:10720516 C>T maps to NM_001079843.1 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:10720516 C>T maps to NM_001079843.1 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:18152848 C>T maps to NM_030812.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:18152848 C>T maps to NM_030812.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:34076830 C>T maps to ENST00000373381 L2011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:34076830 C>T maps to ENST00000373381 L2011L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:43782897 C>A maps to NM_005424.2 S813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:43782897 C>A maps to NM_005424.2 S813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:93159885 C>G maps to NM_005665.4 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:93159885 C>G maps to NM_005665.4 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:150241156 G>A maps to NM_001077628.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:150241156 G>A maps to NM_001077628.1 F18F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:154527963 G>A maps to NM_017582.6 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:154527963 G>A maps to NM_017582.6 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:231472603 C>T maps to NM_175876.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr1:231472603 C>T maps to NM_175876.3 A296A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:20466003 G>T maps to NM_032812.7 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:20466003 G>T maps to NM_032812.7 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:24886939 T>C did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:24886939 T>C did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:62632019 C>T maps to NM_014836.4 W615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:62632019 C>T maps to NM_014836.4 W615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:98129926 C>T maps to NM_012465.3 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:98129926 C>T maps to NM_012465.3 R936R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:124348624 C>A maps to ENST00000368915 S650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr10:124348624 C>A maps to ENST00000368915 S650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr11:703086 C>T maps to ENST00000449452 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr11:703086 C>T maps to ENST00000449452 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr11:6417048 G>A maps to ENST00000389906 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr11:6417048 G>A maps to ENST00000389906 A644A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr11:66328095 G>A maps to NM_001104.1 *577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr11:66328095 G>A maps to NM_001104.1 *577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr12:117658013 C>A maps to ENST00000338101 E1380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr12:117658013 C>A maps to ENST00000338101 E1380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr12:123494553 G>A maps to NM_020845.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr12:123494553 G>A maps to NM_020845.2 F162F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr13:26788557 G>A maps to NM_005977.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr13:26788557 G>A maps to NM_005977.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr13:102029362 G>T maps to NM_052867.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr13:102029362 G>T maps to NM_052867.2 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr14:21788327 C>T maps to NM_020366.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr14:21788327 C>T maps to NM_020366.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr14:52466481 C>T maps to NM_016039.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr14:52466481 C>T maps to NM_016039.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr14:76447098 C>T maps to NM_003239.2 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr14:76447098 C>T maps to NM_003239.2 Q46Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr14:88904623 C>G maps to NM_018418.4 S553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr14:88904623 C>G maps to NM_018418.4 S553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr15:63882964 G>A maps to NM_006537.2 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr15:63882964 G>A maps to NM_006537.2 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:18542929 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:18542929 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:20857631 C>G maps to NM_030941.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:20857631 C>G maps to NM_030941.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:24902256 G>C maps to NM_052944.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:24902256 G>C maps to NM_052944.2 R244R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:50667158 C>T maps to NM_033119.3 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr16:50667158 C>T maps to NM_033119.3 R294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr17:465782 G>A maps to NM_001128159.2 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr17:465782 G>A maps to NM_001128159.2 R506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr17:38645132 G>A maps to NM_032865.5 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr17:38645132 G>A maps to NM_032865.5 F176F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr17:42475271 G>A maps to NM_001002909.2 I1391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr17:42475271 G>A maps to NM_001002909.2 I1391I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr18:67993285 C>A maps to NM_004232.3 S461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr18:67993285 C>A maps to NM_004232.3 S461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:4361722 G>A maps to NM_003025.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:4361722 G>A maps to NM_003025.2 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:11557089 C>A maps to ENST00000436195 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:11557089 C>A maps to ENST00000436195 V229V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:36395530 G>C maps to NM_003332.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:36395530 G>C maps to NM_003332.3 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:40890034 G>A maps to NM_144685.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:40890034 G>A maps to NM_144685.3 F159F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:41522626 C>T maps to NM_000767.4 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:41522626 C>T maps to NM_000767.4 F457F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:50204794 C>T maps to NM_152359.2 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:50204794 C>T maps to NM_152359.2 F199F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:55672017 T>C maps to ENST00000301249 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr19:55672017 T>C maps to ENST00000301249 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr2:102793101 G>A maps to NM_000877.2 W531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr2:102793101 G>A maps to NM_000877.2 W531*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr20:5294781 G>A maps to NM_144773.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr20:5294781 G>A maps to NM_144773.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr21:37741396 C>T maps to ENST00000290384 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr21:37741396 C>T maps to ENST00000290384 V578V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr21:37741837 C>T maps to ENST00000290384 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr21:37741837 C>T maps to ENST00000290384 I725I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr21:47337527 C>A maps to NM_020528.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr21:47337527 C>A maps to NM_020528.2 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr22:39917808 G>A maps to NM_182810.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr22:39917808 G>A maps to NM_182810.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr22:41676973 G>A maps to NM_002883.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr22:41676973 G>A maps to NM_002883.2 F25F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:12198410 G>C maps to NM_003256.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:12198410 G>C maps to NM_003256.2 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:65456103 C>T maps to NM_001033057.1 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:65456103 C>T maps to NM_001033057.1 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:97655688 G>A maps to ENST00000182096 E866E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:97655688 G>A maps to ENST00000182096 E866E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:122259322 C>T maps to NM_031458.2 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:122259322 C>T maps to NM_031458.2 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:183978916 G>A maps to NM_033259.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr3:183978916 G>A maps to NM_033259.2 R53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr4:10083052 C>A maps to NM_017491.3 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr4:10083052 C>A maps to NM_017491.3 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr4:71024283 T>G maps to NM_214711.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr4:71024283 T>G maps to NM_214711.3 P105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr4:141555330 G>C maps to NM_015130.2 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr4:141555330 G>C maps to NM_015130.2 L839L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:41762233 G>A maps to NM_000436.3 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:41762233 G>A maps to NM_000436.3 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:140236853 G>A maps to NM_018901.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:140236853 G>A maps to NM_018901.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:140433382 C>T maps to NM_013340.2 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:140433382 C>T maps to NM_013340.2 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:149755766 G>A maps to ENST00000451292 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:149755766 G>A maps to ENST00000451292 A672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:154272067 C>T maps to NM_015465.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:154272067 C>T maps to NM_015465.3 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:176314514 G>A maps to NM_002115.2 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr5:176314514 G>A maps to NM_002115.2 R513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:4069808 G>C maps to NM_173563.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:4069808 G>C maps to NM_173563.1 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:44218332 C>T maps to NM_007355.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:44218332 C>T maps to NM_007355.2 V318V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:53156761 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:53156761 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:100368917 G>A maps to NM_032503.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr6:100368917 G>A maps to NM_032503.2 I307I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:84651842 C>T maps to NM_152754.2 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:84651842 C>T maps to NM_152754.2 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:100675896 C>T maps to NM_001040105.1 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:100675896 C>T maps to NM_001040105.1 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:104753144 C>T maps to NM_182931.2 Q1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:104753144 C>T maps to NM_182931.2 Q1648*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:137294338 G>C maps to NM_004717.2 S337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:137294338 G>C maps to NM_004717.2 S337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:140273622 C>T maps to NM_015689.3 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr7:140273622 C>T maps to NM_015689.3 K477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr8:77763458 C>T maps to NM_024721.4 F1434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chr8:77763458 C>T maps to NM_024721.4 F1434F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chrX:45013377 G>A maps to NM_176819.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chrX:45013377 G>A maps to NM_176819.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chrX:140994897 C>T maps to NM_005462.4 Q570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chrX:140994897 C>T maps to NM_005462.4 Q570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chrX:153282518 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chrX:153282518 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:16256060 C>G maps to NM_015001.2 S1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:16256060 C>G maps to NM_015001.2 S1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:19479795 G>A maps to ENST00000375267 I2277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:19479795 G>A maps to ENST00000375267 I2277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:19479840 G>A maps to ENST00000375267 V2262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:19479840 G>A maps to ENST00000375267 V2262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:24112167 C>G maps to NM_020362.4 Y108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:24112167 C>G maps to NM_020362.4 Y108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:24413278 C>T maps to ENST00000330966 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:24413278 C>T maps to ENST00000330966 S552S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:94047998 G>A maps to NM_003567.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:94047998 G>A maps to NM_003567.2 F515F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:109477411 C>T maps to NM_001048210.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:109477411 C>T maps to NM_001048210.1 A512A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:115267843 G>C maps to NM_001130523.1 S599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:115267843 G>C maps to NM_001130523.1 S599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:158639537 G>A maps to NM_003126.2 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:158639537 G>A maps to NM_003126.2 D546D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:167088638 G>T maps to NM_001080426.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:167088638 G>T maps to NM_001080426.1 V197V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:170967417 G>A maps to NM_025063.2 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:170967417 G>A maps to NM_025063.2 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:179561977 G>A maps to ENST00000444136 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:179561977 G>A maps to ENST00000444136 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:180165520 C>T maps to NM_002826.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:180165520 C>T maps to NM_002826.4 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:228645862 C>G maps to NM_175055.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:228645862 C>G maps to NM_175055.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:231376776 G>T maps to ENST00000421623 Y37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr1:231376776 G>T maps to ENST00000421623 Y37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr10:94675627 A>G maps to NM_019053.4 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr10:94675627 A>G maps to NM_019053.4 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr10:104375150 C>G maps to NM_016169.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr10:104375150 C>G maps to NM_016169.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:1642999 C>T maps to ENST00000359229 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:1642999 C>T maps to ENST00000359229 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:47290108 G>C maps to NM_005693.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:47290108 G>C maps to NM_005693.2 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:59857927 C>T maps to NM_000139.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:59857927 C>T maps to NM_000139.4 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:66188673 C>T maps to NM_178864.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:66188673 C>T maps to NM_178864.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:75277831 C>T maps to NM_001235.2 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:75277831 C>T maps to NM_001235.2 F146F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:86665890 C>G maps to NM_012193.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr11:86665890 C>G maps to NM_012193.2 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:6752713 G>A maps to NM_032489.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:6752713 G>A maps to NM_032489.2 F356F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:53566402 C>G maps to NM_015989.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:53566402 C>G maps to NM_015989.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:56094854 G>A maps to ENST00000347027 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:56094854 G>A maps to ENST00000347027 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:94676113 C>T maps to NM_005761.1 I1272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:94676113 C>T maps to NM_005761.1 I1272I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:100787218 C>T maps to NM_139319.2 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:100787218 C>T maps to NM_139319.2 Y182Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:105558477 G>A maps to NM_015275.1 K1138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:105558477 G>A maps to NM_015275.1 K1138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:124416303 C>G maps to NM_207437.3 L4228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr12:124416303 C>G maps to NM_207437.3 L4228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr13:110839652 C>T maps to NM_001845.4 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr13:110839652 C>T maps to NM_001845.4 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr14:35872940 C>T maps to NM_020529.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr14:35872940 C>T maps to NM_020529.2 V97V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr14:88442766 G>C maps to NM_000153.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr14:88442766 G>C maps to NM_000153.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr14:90755273 C>T maps to NM_017970.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr14:90755273 C>T maps to NM_017970.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:3828739 C>T maps to NM_004380.2 K634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:3828739 C>T maps to NM_004380.2 K634K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:4432188 G>A maps to NM_138440.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:4432188 G>A maps to NM_138440.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:15155746 C>A maps to NM_018427.3 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:15155746 C>A maps to NM_018427.3 E604*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:22132908 C>T maps to NM_173615.3 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:22132908 C>T maps to NM_173615.3 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:48125045 G>C maps to NM_033226.2 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:48125045 G>C maps to NM_033226.2 L1090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:48130713 C>T maps to NM_033226.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:48130713 C>T maps to NM_033226.2 L1046L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:58621281 C>G maps to NM_016284.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:58621281 C>G maps to NM_016284.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:64984721 G>T maps to NM_001797.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr16:64984721 G>T maps to NM_001797.2 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr17:1551690 G>C maps to NM_031430.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr17:1551690 G>C maps to NM_031430.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr17:7695327 G>T maps to NM_020877.2 E2332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr17:7695327 G>T maps to NM_020877.2 E2332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr17:61559096 C>T maps to NM_000789.3 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr17:61559096 C>T maps to NM_000789.3 F372F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr18:13731929 G>A maps to NM_003799.1 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr18:13731929 G>A maps to NM_003799.1 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr18:34855192 G>A maps to NM_020180.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr18:34855192 G>A maps to NM_020180.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr18:61262336 C>A maps to NM_012397.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr18:61262336 C>A maps to NM_012397.3 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr18:67992740 C>T maps to NM_004232.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr18:67992740 C>T maps to NM_004232.3 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:9059311 C>T maps to NM_024690.2 S9378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:9059311 C>T maps to NM_024690.2 S9378S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:44740264 C>G maps to NM_182490.1 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:44740264 C>G maps to NM_182490.1 S561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:52496663 G>C maps to ENST00000354939 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:52496663 G>C maps to ENST00000354939 L566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:53855450 C>G maps to NM_138374.1 S508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:53855450 C>G maps to NM_138374.1 S508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:54327206 G>C maps to ENST00000391773 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:54327206 G>C maps to ENST00000391773 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:54782201 G>A maps to ENST00000391747 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:54782201 G>A maps to ENST00000391747 H407H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:56702269 C>T maps to NM_001080456.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr19:56702269 C>T maps to NM_001080456.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:27565858 G>A maps to NM_001521.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:27565858 G>A maps to NM_001521.2 L135L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:27565899 G>T maps to NM_001521.2 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:27565899 G>T maps to NM_001521.2 S121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:32889466 G>A maps to NM_017735.4 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:32889466 G>A maps to NM_017735.4 E246E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:128628867 G>C maps to NM_031445.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:128628867 G>C maps to NM_031445.2 S158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:152695760 G>A maps to NM_000726.3 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:152695760 G>A maps to NM_000726.3 Q479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:178097217 C>A maps to NM_006164.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:178097217 C>A maps to NM_006164.3 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:215855599 A>C maps to NM_173076.2 Y1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr2:215855599 A>C maps to NM_173076.2 Y1150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr20:35675482 G>C maps to NM_002895.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr20:35675482 G>C maps to NM_002895.2 L526L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr22:30860843 C>G maps to NM_174975.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr22:30860843 C>G maps to NM_174975.4 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:48309747 C>G maps to NM_016089.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:48309747 C>G maps to NM_016089.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:48423301 C>T maps to NM_207102.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:48423301 C>T maps to NM_207102.2 F366F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:126737154 G>T maps to NM_032242.3 E1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:126737154 G>T maps to NM_032242.3 E1227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:156192550 G>A maps to NM_172159.3 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:156192550 G>A maps to NM_172159.3 Q182Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:167508189 C>G maps to NM_005025.4 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:167508189 C>G maps to NM_005025.4 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:179294462 C>T maps to NM_004301.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:179294462 C>T maps to NM_004301.3 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:183963306 G>T maps to NM_005787.5 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr3:183963306 G>T maps to NM_005787.5 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:8055962 G>A maps to NM_001130083.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:8055962 G>A maps to NM_001130083.1 I258I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:100237127 G>T maps to NM_000668.4 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:100237127 G>T maps to NM_000668.4 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:111542525 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:111542525 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:138453179 G>A maps to NM_019035.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:138453179 G>A maps to NM_019035.3 F21F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:169433386 G>A maps to NM_001166108.1 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:169433386 G>A maps to NM_001166108.1 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:187540002 G>A maps to ENST00000260147 F2582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:187540002 G>A maps to ENST00000260147 F2582F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:189068345 C>T maps to NM_178556.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr4:189068345 C>T maps to NM_178556.3 V409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr5:140263676 G>A maps to NM_018904.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr5:140263676 G>A maps to NM_018904.2 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr5:140744562 C>G maps to NM_018918.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr5:140744562 C>G maps to NM_018918.2 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr5:140755497 T>C maps to NM_018919.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr5:140755497 T>C maps to NM_018919.2 L616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:26045823 G>A maps to NM_003531.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:26045823 G>A maps to NM_003531.2 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:27419368 G>A maps to NM_007149.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:27419368 G>A maps to NM_007149.2 L657L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:30691825 G>A maps to NM_178014.2 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:30691825 G>A maps to NM_178014.2 Q329Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:32137053 C>T maps to NM_032741.4 *284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:32137053 C>T maps to NM_032741.4 *284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:46657052 G>A maps to NM_001010870.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:46657052 G>A maps to NM_001010870.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:128403633 C>T maps to ENST00000368210 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:128403633 C>T maps to ENST00000368210 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:137519720 G>C maps to NM_000416.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:137519720 G>C maps to NM_000416.2 S306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:144508375 C>T maps to NM_003764.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr6:144508375 C>T maps to NM_003764.3 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:7412989 C>T maps to NM_001037763.2 V849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:7412989 C>T maps to NM_001037763.2 V849V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:37298895 C>T maps to NM_014800.9 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:37298895 C>T maps to NM_014800.9 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:55214392 C>G maps to NM_005228.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:55214392 C>G maps to NM_005228.3 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:95217137 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:95217137 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:99725635 G>C maps to NM_203397.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:99725635 G>C maps to NM_203397.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:110526717 G>A maps to NM_032549.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:110526717 G>A maps to NM_032549.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:131082108 C>T maps to NM_013255.4 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:131082108 C>T maps to NM_013255.4 Q162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:151845150 C>A maps to ENST00000355193 E4678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr7:151845150 C>A maps to ENST00000355193 E4678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr8:30889905 C>G maps to NM_013357.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr8:30889905 C>G maps to NM_013357.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr8:71128947 G>A maps to NM_006540.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr8:71128947 G>A maps to NM_006540.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr8:142367297 G>A maps to NM_005293.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr8:142367297 G>A maps to NM_005293.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr9:117185764 C>T maps to NM_015404.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chr9:117185764 C>T maps to NM_015404.3 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:11207063 G>A maps to NM_013427.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:11207063 G>A maps to NM_013427.2 V287V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:24024243 C>T maps to NM_030624.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:24024243 C>T maps to NM_030624.2 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:105152803 C>T maps to NM_198465.2 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:105152803 C>T maps to NM_198465.2 Q391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:105153048 G>C maps to NM_198465.2 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:105153048 G>C maps to NM_198465.2 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:129041399 G>A maps to NM_006649.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:129041399 G>A maps to NM_006649.3 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:149931143 C>A maps to NM_003828.2 S647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:149931143 C>A maps to NM_003828.2 S647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:152938519 C>G maps to NM_001039582.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:152938519 C>G maps to NM_001039582.3 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:153696207 T>G maps to NM_017514.3 G1228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BL-01A-11D-A13W-08 chrX:153696207 T>G maps to NM_017514.3 G1228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:77685078 G>A maps to NM_005482.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:77685078 G>A maps to NM_005482.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:107937832 C>T maps to NM_001113226.1 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:107937832 C>T maps to NM_001113226.1 C315C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:151021204 C>T maps to NM_017860.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:151021204 C>T maps to NM_017860.3 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:205027455 C>T maps to NM_005076.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr1:205027455 C>T maps to NM_005076.3 V121V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr10:75258748 G>A maps to NM_152586.3 Q1565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr10:75258748 G>A maps to NM_152586.3 Q1565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr10:89685299 C>G maps to NM_000314.4 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr10:89685299 C>G maps to NM_000314.4 Y65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr10:98714982 C>T maps to NM_001170765.1 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr10:98714982 C>T maps to NM_001170765.1 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr11:117150912 G>A maps to NM_207343.2 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr11:117150912 G>A maps to NM_207343.2 E361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:20782868 C>G maps to NM_000921.3 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:20782868 C>G maps to NM_000921.3 S523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:49427594 G>C maps to NM_003482.3 L3631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:49427594 G>C maps to NM_003482.3 L3631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:49427851 G>A maps to NM_003482.3 Q3580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:49427851 G>A maps to NM_003482.3 Q3580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:50384051 C>T maps to NM_013277.3 *633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:50384051 C>T maps to NM_013277.3 *633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:52168058 C>A maps to NM_014191.2 I1244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:52168058 C>A maps to NM_014191.2 I1244I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:57921756 C>G maps to NM_052897.3 S788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:57921756 C>G maps to NM_052897.3 S788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:104522199 A>T did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:104522199 A>T did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:114386650 G>A maps to NM_016196.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr12:114386650 G>A maps to NM_016196.3 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr14:100615442 G>A maps to NM_206918.2 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr15:41768711 G>A maps to NM_015138.4 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr15:41768711 G>A maps to NM_015138.4 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr15:64204181 G>A maps to NM_014326.3 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr15:64204181 G>A maps to NM_014326.3 F319F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:7155833 G>T maps to NM_203414.1 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:7155833 G>T maps to NM_203414.1 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:41244493 G>A maps to ENST00000471181 N1018N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:41244493 G>A maps to ENST00000471181 N1018N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:62020420 C>T maps to NM_000334.4 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:62020420 C>T maps to NM_000334.4 T1351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:72245513 G>A maps to NM_032646.5 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:72245513 G>A maps to NM_032646.5 Q302Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:76501503 G>C maps to ENST00000389840 L1605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr17:76501503 G>C maps to ENST00000389840 L1605L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr18:19192398 C>G maps to NM_006938.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr18:19192398 C>G maps to NM_006938.2 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:1062281 G>C maps to NM_019112.3 L1894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:1062281 G>C maps to NM_019112.3 L1894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:14040432 G>A maps to NM_017721.4 Q890Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:14040432 G>A maps to NM_017721.4 Q890Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:22585687 T>A did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:22585687 T>A did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:36508768 C>T maps to NM_015526.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:36508768 C>T maps to NM_015526.2 G436G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:53644385 T>A maps to NM_001172674.1 G566G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:58472917 G>A maps to NM_152474.4 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr19:58472917 G>A maps to NM_152474.4 R125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:20189767 G>A maps to NM_001006657.1 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:20189767 G>A maps to NM_001006657.1 F3F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:69554096 C>T maps to ENST00000357308 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:69554096 C>T maps to ENST00000357308 V668V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:96970570 G>A maps to NM_014014.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:96970570 G>A maps to NM_014014.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:202074060 C>T maps to NM_032977.3 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:202074060 C>T maps to NM_032977.3 F397F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:219321884 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:219321884 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:223423364 C>G maps to NM_152386.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr2:223423364 C>G maps to NM_152386.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr22:21188889 T>C maps to NM_058004.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr22:21188889 T>C maps to NM_058004.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr22:43565514 C>T maps to NM_015140.3 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr22:43565514 C>T maps to NM_015140.3 T545T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr3:52437781 G>C maps to NM_004656.2 S460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr3:52437781 G>C maps to NM_004656.2 S460*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr3:132278759 T>G maps to NM_032169.4 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr3:132278759 T>G maps to NM_032169.4 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:2514237 C>T maps to NM_002938.4 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:2514237 C>T maps to NM_002938.4 D96D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:9784378 C>T maps to NM_000798.4 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:9784378 C>T maps to NM_000798.4 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:94750667 A>G maps to NM_005172.1 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:94750667 A>G maps to NM_005172.1 K197K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:109895697 T>C maps to ENST00000333642 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:109895697 T>C maps to ENST00000333642 K152K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:140264025 C>A maps to NM_057175.3 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr4:140264025 C>A maps to NM_057175.3 S150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr5:52206173 G>C maps to NM_181501.1 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr5:52206173 G>C maps to NM_181501.1 P594P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr5:115351426 C>T maps to NM_173800.4 D907D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr5:115351426 C>T maps to NM_173800.4 D907D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr5:145895352 C>T maps to NM_194251.2 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr5:145895352 C>T maps to NM_194251.2 W108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr5:171299925 G>A maps to NM_012300.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr5:171299925 G>A maps to NM_012300.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:31890314 G>C maps to NM_001191057.1 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:31890314 G>C maps to NM_001191057.1 S264*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:84751141 C>T maps to NM_152754.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:84751141 C>T maps to NM_152754.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:99051699 C>T maps to NM_006693.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:99051699 C>T maps to NM_006693.2 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:101844748 C>T maps to ENST00000360264 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr7:101844748 C>T maps to ENST00000360264 L735L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr8:43025772 C>T maps to ENST00000458501 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BM-01A-11D-A13W-08 chr8:43025772 C>T maps to ENST00000458501 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:3319364 G>A maps to NM_022114.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:3319364 G>A maps to NM_022114.3 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:87038328 C>T maps to ENST00000263723 Q465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr1:87038328 C>T maps to ENST00000263723 Q465*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr10:64943285 G>C maps to NM_032776.1 L2335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr10:64943285 G>C maps to NM_032776.1 L2335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr10:121586538 A>T maps to NM_014937.2 V882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr10:121586538 A>T maps to NM_014937.2 V882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr11:120186098 C>G maps to NM_014352.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr11:120186098 C>G maps to NM_014352.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr12:58019064 C>T maps to NM_133489.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr12:58019064 C>T maps to NM_133489.2 T475T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr14:69349242 C>A maps to NM_001130004.1 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr14:69349242 C>A maps to NM_001130004.1 E629*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr15:52188683 C>T maps to NM_014547.4 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr15:52188683 C>T maps to NM_014547.4 F232F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr16:15704956 G>C maps to NM_014647.3 S1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr16:15704956 G>C maps to NM_014647.3 S1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr17:27075425 C>G maps to NM_004295.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr17:27075425 C>G maps to NM_004295.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr17:44115925 G>T maps to NM_015443.3 S840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr17:44115925 G>T maps to NM_015443.3 S840*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr19:38976784 C>T maps to NM_000540.2 V1830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr19:38976784 C>T maps to NM_000540.2 V1830V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:1805481 T>A maps to ENST00000399161 K1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:1805481 T>A maps to ENST00000399161 K1088*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:74902125 C>T maps to NM_004263.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:74902125 C>T maps to NM_004263.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:233899463 C>T maps to NM_005383.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr2:233899463 C>T maps to NM_005383.2 P280P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1BN-01B-11D-A14W-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-C5-A1BN-01B-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr22:50582542 G>A maps to NM_018995.2 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr22:50582542 G>A maps to NM_018995.2 P792P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr3:129247935 C>T maps to NM_000539.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr3:129247935 C>T maps to NM_000539.3 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr3:169496993 C>A maps to NM_018657.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr3:169496993 C>A maps to NM_018657.4 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr6:29408112 C>T maps to NM_013941.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr6:29408112 C>T maps to NM_013941.2 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr6:116757049 C>T maps to NM_013352.2 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr6:116757049 C>T maps to NM_013352.2 Y473Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr6:139241453 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr6:139241453 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr8:104973323 T>C maps to NM_001100117.2 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr8:104973323 T>C maps to NM_001100117.2 S911S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr9:136277935 G>A maps to NM_020385.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chr9:136277935 G>A maps to NM_020385.2 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chrX:75649150 C>A maps to NM_020932.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chrX:75649150 C>A maps to NM_020932.2 A276A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chrX:105451165 A>C maps to NM_001171020.1 R581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chrX:105451165 A>C maps to NM_001171020.1 R581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chrX:132161142 G>T maps to NM_031907.1 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chrX:132161142 G>T maps to NM_031907.1 S369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chrX:141291725 G>C maps to NM_016249.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BN-01B-11D-A14W-08 chrX:141291725 G>C maps to NM_016249.3 S16S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:3775313 C>T maps to ENST00000430539 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:3775313 C>T maps to ENST00000430539 Y49Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:48703473 C>T maps to NM_001135181.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:48703473 C>T maps to NM_001135181.1 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:115829245 C>T maps to NM_002506.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:115829245 C>T maps to NM_002506.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:223396681 C>T maps to NM_017982.3 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:223396681 C>T maps to NM_017982.3 E451E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:241798675 G>A maps to NM_001821.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr1:241798675 G>A maps to NM_001821.3 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr10:7745453 C>T maps to NM_002216.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr10:7745453 C>T maps to NM_002216.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr10:43692547 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr10:43692547 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr10:70748635 G>A maps to NM_015634.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr10:70748635 G>A maps to NM_015634.3 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr10:105372775 G>A maps to ENST00000369774 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr10:105372775 G>A maps to ENST00000369774 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr10:134219455 C>T maps to NM_138499.3 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr10:134219455 C>T maps to NM_138499.3 D484D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr11:63670178 C>T maps to NM_001039469.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr11:63670178 C>T maps to NM_001039469.2 A447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr12:49994423 C>T maps to NM_032130.2 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr12:49994423 C>T maps to NM_032130.2 E333E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr13:36396958 G>A maps to NM_004734.4 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr13:36396958 G>A maps to NM_004734.4 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr16:24358138 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr16:24358138 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr17:6716197 C>T maps to NM_053285.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr17:6716197 C>T maps to NM_053285.1 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr18:9950483 C>T maps to NM_003574.5 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr18:9950483 C>T maps to NM_003574.5 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr19:4511412 C>T maps to NM_001080400.1 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr19:4511412 C>T maps to NM_001080400.1 T839T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr19:56701804 C>G maps to NM_001080456.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr19:56701804 C>G maps to NM_001080456.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr2:85554083 A>C maps to ENST00000409015 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr2:85554083 A>C maps to ENST00000409015 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr2:128324315 C>T maps to ENST00000389524 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr2:128324315 C>T maps to ENST00000389524 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr2:210557805 G>A maps to NM_002374.3 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr2:210557805 G>A maps to NM_002374.3 W304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr20:17596582 G>A maps to ENST00000377813 A1313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr20:17596582 G>A maps to ENST00000377813 A1313A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr20:34263074 G>A maps to NM_021100.4 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr20:34263074 G>A maps to NM_021100.4 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr21:44488637 G>A maps to ENST00000398168 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr21:44488637 G>A maps to ENST00000398168 F99F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr22:30776080 C>T maps to NM_001017981.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr22:30776080 C>T maps to NM_001017981.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr22:44234842 G>A maps to NM_014351.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr22:44234842 G>A maps to NM_014351.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:38022264 G>A maps to NM_001008392.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:38022264 G>A maps to NM_001008392.1 T246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:49758727 C>A maps to NM_022064.2 S1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:49758727 C>A maps to NM_022064.2 S1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:62556597 G>A maps to ENST00000383709 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:62556597 G>A maps to ENST00000383709 I531I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:98109724 C>T maps to NM_001005516.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:98109724 C>T maps to NM_001005516.1 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:130720085 C>T maps to NM_001001486.1 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr3:130720085 C>T maps to NM_001001486.1 L884L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr4:52883761 G>A maps to NM_001024611.1 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr4:52883761 G>A maps to NM_001024611.1 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr4:140281652 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr4:140281652 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr5:42718862 A>G maps to NM_000163.2 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr5:42718862 A>G maps to NM_000163.2 K418K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr7:14758206 C>T maps to NM_004080.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr7:14758206 C>T maps to NM_004080.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr7:100675494 A>G maps to NM_001040105.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr7:100675494 A>G maps to NM_001040105.1 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr7:151962240 G>A maps to ENST00000355193 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr7:151962240 G>A maps to ENST00000355193 Q356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr8:63976818 G>A maps to NM_000370.3 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr8:63976818 G>A maps to NM_000370.3 F203F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr9:35560822 C>T maps to NM_001135999.1 Q1396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chr9:35560822 C>T maps to NM_001135999.1 Q1396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chrX:127186236 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M5-01A-11D-A13W-08 chrX:127186236 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:28861791 G>A maps to NM_001048194.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:28861791 G>A maps to NM_001048194.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:40726593 C>G maps to NM_005857.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:40726593 C>G maps to NM_005857.3 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:45363061 C>T maps to NM_020365.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:45363061 C>T maps to NM_020365.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:101704599 C>T maps to NM_001400.4 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:101704599 C>T maps to NM_001400.4 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:146736154 C>T maps to NM_004284.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:146736154 C>T maps to NM_004284.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:160262344 G>A maps to NM_001098398.1 Y972Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:160262344 G>A maps to NM_001098398.1 Y972Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:170705269 G>C maps to NM_022716.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:170705269 G>C maps to NM_022716.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:173840187 G>T maps to NM_001122770.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr1:173840187 G>T maps to NM_001122770.1 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr10:15649713 T>A maps to NM_003638.1 K576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr10:15649713 T>A maps to NM_003638.1 K576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr10:49459668 C>A maps to NM_001018071.3 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr10:49459668 C>A maps to NM_001018071.3 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr10:111651525 G>C maps to NM_020383.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr10:111651525 G>C maps to NM_020383.3 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr11:57569477 C>T maps to NM_001085458.1 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr11:57569477 C>T maps to NM_001085458.1 I410I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr11:62601345 G>C maps to NM_018093.2 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr11:62601345 G>C maps to NM_018093.2 S280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr11:68341594 G>A maps to NM_001164160.1 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr11:68341594 G>A maps to NM_001164160.1 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr11:107943061 T>G maps to NM_003478.3 L293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr11:107943061 T>G maps to NM_003478.3 L293*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1M6-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr12:6776899 C>A maps to NM_001135734.1 E572*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1M6-01A-11D-A13W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr12:6776899 C>A maps to NM_001135734.1 E572*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr12:9085315 C>G maps to ENST00000433083 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr12:9085315 C>G maps to ENST00000433083 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr14:24545479 G>A maps to NM_006032.2 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr14:24545479 G>A maps to NM_006032.2 Q349Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr14:102466694 C>T maps to NM_001376.4 Q1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr14:102466694 C>T maps to NM_001376.4 Q1345*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr15:62942298 C>T maps to NM_015059.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr15:62942298 C>T maps to NM_015059.2 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr16:1793356 G>A maps to NM_015133.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr16:1793356 G>A maps to NM_015133.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr16:67179510 G>A maps to NM_025187.3 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr16:67179510 G>A maps to NM_025187.3 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr16:67902435 C>T maps to NM_005796.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr16:67902435 C>T maps to NM_005796.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:6919819 G>A maps to NM_001142798.1 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:6919819 G>A maps to NM_001142798.1 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:7578381 G>C maps to NM_001126112.1 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:7690335 C>T maps to NM_020877.2 I2196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:7690335 C>T maps to NM_020877.2 I2196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:17772739 G>A maps to NM_001082968.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:17772739 G>A maps to NM_001082968.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:48761447 C>T maps to NM_003786.3 Q1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:48761447 C>T maps to NM_003786.3 Q1365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:57958297 G>C maps to NM_016261.3 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:57958297 G>C maps to NM_016261.3 S165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:72943104 C>A maps to NM_178233.1 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr17:72943104 C>A maps to NM_178233.1 T385T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr18:18562726 G>A maps to NM_005406.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr18:18562726 G>A maps to NM_005406.2 F852F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:3977936 G>A maps to NM_001961.3 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:3977936 G>A maps to NM_001961.3 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:16045203 G>A maps to NM_021187.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:16045203 G>A maps to NM_021187.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:31770290 G>A maps to NM_020856.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:31770290 G>A maps to NM_020856.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:33096836 C>T maps to NM_032139.2 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:33096836 C>T maps to NM_032139.2 S799S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:38200718 G>C maps to NM_032689.4 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:38200718 G>C maps to NM_032689.4 S5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:44501187 C>T maps to NM_003445.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:44501187 C>T maps to NM_003445.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:44740133 G>A maps to NM_182490.1 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:44740133 G>A maps to NM_182490.1 E517E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:51228561 C>T maps to NM_002975.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr19:51228561 C>T maps to NM_002975.2 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr2:37349710 C>T maps to NM_001135651.1 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr2:37349710 C>T maps to NM_001135651.1 E335E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr2:44123817 C>T maps to NM_133259.3 P1285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr2:44123817 C>T maps to NM_133259.3 P1285P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr2:44190815 C>A maps to NM_133259.3 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr2:44190815 C>A maps to NM_133259.3 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr2:108881767 G>A maps to NM_001008743.1 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr2:108881767 G>A maps to NM_001008743.1 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr20:50407562 G>A maps to NM_020436.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr20:50407562 G>A maps to NM_020436.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr21:32598164 G>C maps to NM_003253.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr21:32598164 G>C maps to NM_003253.2 L562L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:42132993 C>T maps to NM_001042646.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:42132993 C>T maps to NM_001042646.1 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:108288400 G>A maps to NM_020890.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:108288400 G>A maps to NM_020890.2 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:129284293 G>A maps to NM_015103.2 L1470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:129284293 G>A maps to NM_015103.2 L1470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:191047504 C>G maps to NM_178335.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:191047504 C>G maps to NM_178335.2 V14V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:193380645 G>A maps to NM_130837.2 K852K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr3:193380645 G>A maps to NM_130837.2 K852K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr4:82088332 G>A maps to NM_006259.1 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr4:82088332 G>A maps to NM_006259.1 I298I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr5:131977956 T>G maps to NM_005732.3 S1280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr5:131977956 T>G maps to NM_005732.3 S1280S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr5:135513102 C>T maps to NM_001001419.1 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr5:135513102 C>T maps to NM_001001419.1 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr5:135513157 C>T maps to NM_001001419.1 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr5:135513157 C>T maps to NM_001001419.1 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr5:150497333 G>A maps to NM_001155.4 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr5:150497333 G>A maps to NM_001155.4 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr6:99283887 C>A maps to NM_005604.2 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr6:99283887 C>A maps to NM_005604.2 S380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr7:100355922 C>T maps to ENST00000349350 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr7:100355922 C>T maps to ENST00000349350 T1136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr7:111368506 C>T maps to ENST00000428084 R1917R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr7:111368506 C>T maps to ENST00000428084 R1917R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr8:42044947 G>A maps to NM_000930.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr8:42044947 G>A maps to NM_000930.3 I169I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr8:124359380 C>T maps to NM_014109.3 Q721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr8:124359380 C>T maps to NM_014109.3 Q721Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr9:84608576 G>C maps to NM_001001670.2 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chr9:84608576 G>C maps to NM_001001670.2 L1064L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chrX:48840189 C>T maps to NM_020137.3 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chrX:48840189 C>T maps to NM_020137.3 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chrX:139586892 C>T maps to NM_005634.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M6-01A-11D-A13W-08 chrX:139586892 C>T maps to NM_005634.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:8399733 C>A maps to ENST00000377479 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:8399733 C>A maps to ENST00000377479 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:20998568 C>A maps to NM_020816.2 E862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:20998568 C>A maps to NM_020816.2 E862*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:109394360 G>C maps to NM_152763.3 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:109394360 G>C maps to NM_152763.3 S309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:120342437 C>T maps to NM_032044.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:120342437 C>T maps to NM_032044.3 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:152286054 G>C maps to NM_002016.1 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:152286054 G>C maps to NM_002016.1 S436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:153920585 C>T maps to NM_181715.2 *694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:153920585 C>T maps to NM_181715.2 *694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:156177683 C>T maps to NM_014655.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:156177683 C>T maps to NM_014655.2 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:158636104 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:158636104 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:215749312 T>C maps to NM_016121.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:215749312 T>C maps to NM_016121.3 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:222712017 G>A maps to NM_024746.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr1:222712017 G>A maps to NM_024746.3 L517L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr10:29762859 G>C maps to NM_021738.2 V1812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr10:29762859 G>C maps to NM_021738.2 V1812V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr10:61835653 G>C maps to NM_020987.2 S1662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr10:61835653 G>C maps to NM_020987.2 S1662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr10:75608804 G>A maps to ENST00000423381 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr10:75608804 G>A maps to ENST00000423381 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr11:45671567 G>A maps to NM_003654.4 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr11:45671567 G>A maps to NM_003654.4 Y302Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr11:45882476 C>A maps to NM_021117.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr11:45882476 C>A maps to NM_021117.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr11:118983582 A>G maps to NM_014807.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr11:118983582 A>G maps to NM_014807.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr12:56618690 G>A maps to NM_024068.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr12:56618690 G>A maps to NM_024068.3 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr12:57677634 G>A maps to ENST00000438036 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr12:57677634 G>A maps to ENST00000438036 G399G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr12:104522199 A>T did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr12:104522199 A>T did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr13:50097351 G>A maps to NM_001040443.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr13:50097351 G>A maps to NM_001040443.1 V204V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr13:52346017 C>T maps to NM_001031719.1 W166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr13:52346017 C>T maps to NM_001031719.1 W166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr13:52952232 C>T maps to NM_018676.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr13:52952232 C>T maps to NM_018676.3 L624L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr13:113729376 C>T maps to NM_001112732.1 Y451Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr13:113729376 C>T maps to NM_001112732.1 Y451Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr14:31358870 G>C maps to NM_004086.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr14:31358870 G>C maps to NM_004086.2 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr14:75580937 A>G maps to NM_033116.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr14:75580937 A>G maps to NM_033116.4 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr15:41797682 G>A maps to NM_002344.5 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr15:41797682 G>A maps to NM_002344.5 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr16:16180760 C>T maps to ENST00000399408 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr16:16180760 C>T maps to ENST00000399408 F791F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr16:29899990 C>T maps to NM_201575.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr16:29899990 C>T maps to NM_201575.2 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:74568853 G>C maps to NM_006456.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:74568853 G>C maps to NM_006456.2 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:76120083 G>A maps to NM_007267.6 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:76120083 G>A maps to NM_007267.6 I356I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:76120119 G>C maps to NM_007267.6 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:76120119 G>C maps to NM_007267.6 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:79073864 G>A maps to NM_017451.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:79073864 G>A maps to NM_017451.2 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:79827244 C>A maps to NM_004309.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:79827244 C>A maps to NM_004309.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:80963068 C>T maps to NM_001009905.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr17:80963068 C>T maps to NM_001009905.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:38804674 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:38804674 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:103040289 C>G maps to NM_003853.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:103040289 C>G maps to NM_003853.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:103040353 C>T maps to NM_003853.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:103040353 C>T maps to NM_003853.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:202619286 C>A maps to NM_020919.3 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:202619286 C>A maps to NM_020919.3 E527*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:206630244 C>A maps to NM_201266.1 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr2:206630244 C>A maps to NM_201266.1 A785A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr20:35748154 G>C maps to ENST00000343811 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr20:35748154 G>C maps to ENST00000343811 L798L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr20:44665957 C>T maps to NM_001134771.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr20:44665957 C>T maps to NM_001134771.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr21:45978217 G>A maps to NM_198696.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr21:45978217 G>A maps to NM_198696.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr22:51183145 C>T maps to NM_001097.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr22:51183145 C>T maps to NM_001097.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr3:132319906 C>T maps to NM_178445.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr3:132319906 C>T maps to NM_178445.1 I222I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr4:1730121 G>C maps to NM_006342.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr4:1730121 G>C maps to NM_006342.1 S331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr4:71588331 C>T maps to NM_001037442.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr4:71588331 C>T maps to NM_001037442.2 T14T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr5:80626632 G>A maps to NM_130767.2 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr5:80626632 G>A maps to NM_130767.2 I506I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr5:140176540 C>T maps to NM_018905.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr5:140176540 C>T maps to NM_018905.2 T664T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr6:43591720 G>A maps to NM_019096.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr6:43591720 G>A maps to NM_019096.3 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr7:27170292 G>A maps to NM_002141.4 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr7:27170292 G>A maps to NM_002141.4 F20F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr7:95157137 C>T maps to NM_016116.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr7:95157137 C>T maps to NM_016116.2 N167N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr7:98574695 G>A maps to ENST00000359863 E2787E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr7:98574695 G>A maps to ENST00000359863 E2787E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr9:132397622 C>T maps to NM_014064.2 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chr9:132397622 C>T maps to NM_014064.2 C184C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chrX:100911644 G>T maps to NM_177949.2 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chrX:100911644 G>T maps to NM_177949.2 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chrX:140969326 C>A maps to NM_138702.1 Y218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M7-01A-11D-A13W-08 chrX:140969326 C>A maps to NM_138702.1 Y218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:10197128 C>T maps to NM_001105562.2 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:10197128 C>T maps to NM_001105562.2 G743G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:91403561 A>G maps to NM_201269.1 H1056H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:91403561 A>G maps to NM_201269.1 H1056H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:169697036 C>T maps to NM_000450.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:169697036 C>T maps to NM_000450.2 P437P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:213032465 C>T maps to NM_014053.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:213032465 C>T maps to NM_014053.2 I224I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:214549656 G>A maps to NM_005401.4 R938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:214549656 G>A maps to NM_005401.4 R938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:229667458 C>T maps to NM_012089.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr1:229667458 C>T maps to NM_012089.2 S453S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr10:24908765 A>C maps to NM_020824.3 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr10:24908765 A>C maps to NM_020824.3 S686S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr11:27136997 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr11:27136997 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr14:77319572 G>A maps to NM_194287.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr14:77319572 G>A maps to NM_194287.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr15:77472801 G>A maps to NM_024776.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr15:77472801 G>A maps to NM_024776.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr17:7406711 C>G maps to NM_000937.4 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr17:7406711 C>G maps to NM_000937.4 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr17:11511459 C>T maps to NM_001372.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr17:11511459 C>T maps to NM_001372.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr17:62529077 G>A maps to NM_138363.1 K598K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr17:62529077 G>A maps to NM_138363.1 K598K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr18:51892103 C>T maps to ENST00000382911 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr18:51892103 C>T maps to ENST00000382911 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:12491264 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:12491264 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:21607217 C>G maps to NM_001076678.2 S586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:21607217 C>G maps to NM_001076678.2 S586*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:58384593 G>A maps to NM_001144989.1 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:58384593 G>A maps to NM_001144989.1 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:58564882 G>T maps to NM_182572.3 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr19:58564882 G>T maps to NM_182572.3 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr3:183551374 G>A maps to NM_018622.5 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr3:183551374 G>A maps to NM_018622.5 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr4:123258114 G>A maps to NM_015312.3 S4030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr4:123258114 G>A maps to NM_015312.3 S4030S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr6:31733526 G>A maps to NM_025258.2 T840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr6:31733526 G>A maps to NM_025258.2 T840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr7:100349806 G>A maps to ENST00000349350 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chr7:100349806 G>A maps to ENST00000349350 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chrX:37026575 G>A maps to NM_001013736.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chrX:37026575 G>A maps to NM_001013736.2 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chrX:52826381 T>A maps to NM_001009616.2 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M8-01A-21D-A13W-08 chrX:52826381 T>A maps to NM_001009616.2 K3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr1:232626796 C>T maps to NM_020808.3 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr1:232626796 C>T maps to NM_020808.3 L543L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr10:68280426 G>A maps to NM_013266.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr10:68280426 G>A maps to NM_013266.2 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr15:22990061 G>A maps to NM_014608.2 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr15:22990061 G>A maps to NM_014608.2 L894L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr15:52901517 C>T maps to NM_019600.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr15:52901517 C>T maps to NM_019600.2 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr17:75186916 G>A maps to NM_001039573.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr17:75186916 G>A maps to NM_001039573.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr19:30935509 C>T maps to NM_014717.1 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr19:30935509 C>T maps to NM_014717.1 C347C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr19:57967233 G>T maps to NM_020633.2 Y207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr19:57967233 G>T maps to NM_020633.2 Y207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr2:201507421 A>C maps to NM_001159.3 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr2:201507421 A>C maps to NM_001159.3 P915P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr2:216272871 G>C maps to NM_212482.1 S826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr2:216272871 G>C maps to NM_212482.1 S826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr22:37964250 C>T maps to NM_152243.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr22:37964250 C>T maps to NM_152243.2 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr5:80547052 G>A maps to NM_001825.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr5:80547052 G>A maps to NM_001825.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr6:154567918 G>C maps to NM_001008503.1 *419Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr6:154567918 G>C maps to NM_001008503.1 *419Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr7:149129367 C>T maps to ENST00000440594 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr7:149129367 C>T maps to ENST00000440594 T666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr8:65509396 C>T maps to NM_004820.3 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chr8:65509396 C>T maps to NM_004820.3 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chrX:34657408 G>A maps to NM_031442.3 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chrX:34657408 G>A maps to NM_031442.3 R108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chrX:149638348 C>T maps to NM_005491.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1M9-01A-11D-A13W-08 chrX:149638348 C>T maps to NM_005491.3 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr1:11897156 C>T maps to ENST00000376496 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr1:11897156 C>T maps to ENST00000376496 I694I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr1:150958851 C>A maps to NM_003568.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr1:150958851 C>A maps to NM_003568.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr10:14816479 G>A maps to NM_031453.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr10:14816479 G>A maps to NM_031453.2 G61G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr10:34739376 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr10:34739376 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr11:1643251 A>G maps to ENST00000359229 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr11:1643251 A>G maps to ENST00000359229 C24C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr12:51856146 G>A maps to NM_001039960.1 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr12:51856146 G>A maps to NM_001039960.1 G385G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr12:96063913 C>A maps to NM_021229.3 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr12:96063913 C>A maps to NM_021229.3 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr13:78320889 C>T maps to ENST00000389459 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr13:78320889 C>T maps to ENST00000389459 S364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr14:70512939 G>A maps to NM_183002.1 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr14:70512939 G>A maps to NM_183002.1 I836I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr16:55362885 G>A maps to NM_024335.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr16:55362885 G>A maps to NM_024335.2 A332A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr17:4720322 C>T maps to NM_002663.3 H558H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr17:4720322 C>T maps to NM_002663.3 H558H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr17:40934778 C>A maps to NM_032387.4 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr17:40934778 C>A maps to NM_032387.4 R208R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr19:12858249 G>A maps to NM_004317.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr19:12858249 G>A maps to NM_004317.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr19:58640192 G>A maps to NM_024620.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr19:58640192 G>A maps to NM_024620.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr2:71660367 A>G maps to NM_014497.3 A1942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr2:71660367 A>G maps to NM_014497.3 A1942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr2:109545670 A>T maps to ENST00000376651 C113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr2:109545670 A>T maps to ENST00000376651 C113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr2:149247487 G>A maps to ENST00000404807 Q1429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr2:149247487 G>A maps to ENST00000404807 Q1429Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr2:179483069 A>T maps to NM_133378.4 V13137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr2:179483069 A>T maps to NM_133378.4 V13137V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr20:43559249 G>A maps to NM_001124756.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr20:43559249 G>A maps to NM_001124756.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr21:22710835 G>A maps to NM_004540.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr21:22710835 G>A maps to NM_004540.2 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr22:44359203 A>G maps to NM_015380.4 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr22:44359203 A>G maps to NM_015380.4 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr3:51897274 C>T maps to NM_203424.1 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr3:51897274 C>T maps to NM_203424.1 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr3:65425602 T>C maps to NM_001033057.1 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr3:65425602 T>C maps to NM_001033057.1 Q407Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr4:73943172 G>A maps to NM_032217.3 Q2496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr4:73943172 G>A maps to NM_032217.3 Q2496*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr6:7310257 C>T maps to ENST00000474597 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr6:7310257 C>T maps to ENST00000474597 L28L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr6:47646845 T>C maps to NM_153839.6 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr6:47646845 T>C maps to NM_153839.6 T81T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr6:142758604 G>A maps to NM_198569.2 K1118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr6:142758604 G>A maps to NM_198569.2 K1118K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr7:141802439 G>C maps to ENST00000475668 G2659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ME-01A-11D-A13W-08 chr7:141802439 G>C maps to ENST00000475668 G2659G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:21807445 G>T maps to NM_032264.2 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:21807445 G>T maps to NM_032264.2 E469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:43827909 A>C maps to NM_001255.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:43827909 A>C maps to NM_001255.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:60312833 G>A maps to NM_015888.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:60312833 G>A maps to NM_015888.4 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:190067661 C>T maps to NM_199051.1 W596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:190067661 C>T maps to NM_199051.1 W596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:209791341 C>T maps to NM_000228.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:209791341 C>T maps to NM_000228.2 L987L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:226426769 C>A maps to ENST00000366807 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:226426769 C>A maps to ENST00000366807 E533*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:228003830 C>T maps to NM_183062.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:228003830 C>T maps to NM_183062.2 G63G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:230398691 G>A maps to NM_004481.3 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr1:230398691 G>A maps to NM_004481.3 R418R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr10:7423843 G>C maps to NM_001018039.1 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr10:7423843 G>C maps to NM_001018039.1 S6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr10:13275613 G>A maps to NM_145314.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr10:13275613 G>A maps to NM_145314.1 F48F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr10:120353958 G>A maps to NM_004248.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr10:120353958 G>A maps to NM_004248.2 A266A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr11:5461826 G>C maps to NM_001005288.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr11:5461826 G>C maps to NM_001005288.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr11:36484189 C>T maps to NM_001160167.1 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr11:36484189 C>T maps to NM_001160167.1 S337S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr12:28605542 C>T maps to NM_018318.3 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr12:28605542 C>T maps to NM_018318.3 Q353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr12:45568076 A>T maps to ENST00000256692 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr12:45568076 A>T maps to ENST00000256692 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr13:31205522 G>A maps to NM_005800.4 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr13:31205522 G>A maps to NM_005800.4 S260S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr13:114762092 G>C maps to ENST00000389544 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr13:114762092 G>C maps to ENST00000389544 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr14:21250154 C>A maps to NM_005615.4 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr14:21250154 C>A maps to NM_005615.4 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr14:64491094 C>T maps to NM_182914.2 Q1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr14:64491094 C>T maps to NM_182914.2 Q1920*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr14:103406261 G>A maps to NM_006035.3 D1538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr14:103406261 G>A maps to NM_006035.3 D1538D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr15:62283885 G>T maps to NM_020821.2 S490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr15:62283885 G>T maps to NM_020821.2 S490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr15:86228061 C>T maps to NM_006738.4 F1753F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr15:86228061 C>T maps to NM_006738.4 F1753F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr16:67574373 C>T maps to NM_001193523.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr16:67574373 C>T maps to NM_001193523.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr17:34431240 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr17:34431240 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr17:56540517 C>T maps to NM_001080439.1 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr17:56540517 C>T maps to NM_001080439.1 E389E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr17:74771184 C>T maps to NM_024311.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr17:74771184 C>T maps to NM_024311.2 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr19:3595826 G>A maps to NM_201636.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr19:3595826 G>A maps to NM_201636.2 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr19:10625528 C>T maps to NM_001166215.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr19:10625528 C>T maps to NM_001166215.1 E53E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr19:12076009 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr19:12076009 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr19:17056394 G>A maps to ENST00000443236 I976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr19:17056394 G>A maps to ENST00000443236 I976I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:15307387 C>T maps to NM_015909.2 L2300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:15307387 C>T maps to NM_015909.2 L2300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:67631385 G>A maps to NM_019002.3 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:67631385 G>A maps to NM_019002.3 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:75116396 C>T maps to NM_000189.4 R801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:75116396 C>T maps to NM_000189.4 R801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:88991296 C>T maps to NM_144563.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:88991296 C>T maps to NM_144563.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:179325901 G>A maps to NM_001042702.3 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:179325901 G>A maps to NM_001042702.3 E320E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:179458766 A>G maps to NM_133378.4 R16883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr2:179458766 A>G maps to NM_133378.4 R16883R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr22:42461876 G>T maps to NM_000262.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr22:42461876 G>T maps to NM_000262.2 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:9594297 G>A maps to NM_198560.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:9594297 G>A maps to NM_198560.2 I22I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:147128258 C>G maps to NM_003412.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:147128258 C>G maps to NM_003412.3 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:185252684 C>T maps to NM_139248.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:185252684 C>T maps to NM_139248.2 L95L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:189608647 C>T maps to NM_003722.4 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:189608647 C>T maps to NM_003722.4 Q575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:196089279 G>A maps to NM_015562.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr3:196089279 G>A maps to NM_015562.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr6:26392862 C>T maps to NM_001197237.1 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr6:26392862 C>T maps to NM_001197237.1 Q414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr7:66460332 C>T maps to NM_016038.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chr7:66460332 C>T maps to NM_016038.2 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chrX:100387417 C>G maps to NM_006733.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chrX:100387417 C>G maps to NM_006733.2 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chrX:134292175 G>C maps to NM_001031705.2 S162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MF-01A-11D-A13W-08 chrX:134292175 G>C maps to NM_001031705.2 S162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:1469406 G>A maps to NM_018188.3 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:1469406 G>A maps to NM_018188.3 L620L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:10035737 C>T maps to NM_022787.3 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:10035737 C>T maps to NM_022787.3 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:11561450 G>A maps to NM_020780.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:11561450 G>A maps to NM_020780.1 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:12342892 C>T maps to NM_015378.2 L1578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:12342892 C>T maps to NM_015378.2 L1578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:17318247 G>A maps to NM_022089.2 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:17318247 G>A maps to NM_022089.2 I744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:18703403 C>T maps to NM_032880.4 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:18703403 C>T maps to NM_032880.4 A404A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:19436712 G>A maps to ENST00000375267 L3994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:19436712 G>A maps to ENST00000375267 L3994L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:22168564 G>A maps to NM_005529.5 F3041F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:22168564 G>A maps to NM_005529.5 F3041F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:23688743 G>A maps to NM_001077195.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:23688743 G>A maps to NM_001077195.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:24388455 G>C maps to ENST00000330966 S1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:24388455 G>C maps to ENST00000330966 S1308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:26161932 G>A maps to NM_024037.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:26161932 G>A maps to NM_024037.1 Q209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:28285126 C>T maps to NM_014474.2 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:28285126 C>T maps to NM_014474.2 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:28661063 C>T maps to NM_017638.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:28661063 C>T maps to NM_017638.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:41475252 C>G maps to NM_001905.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:41475252 C>G maps to NM_001905.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:45271328 C>T maps to NM_004073.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:45271328 C>T maps to NM_004073.2 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:54238060 G>A maps to NM_018087.4 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:54238060 G>A maps to NM_018087.4 F634F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:65854987 C>T maps to ENST00000371069 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:65854987 C>T maps to ENST00000371069 Q415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:67147792 C>G maps to ENST00000237247 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:67147792 C>G maps to ENST00000237247 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:82431797 C>T maps to ENST00000370717 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:82431797 C>T maps to ENST00000370717 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:85624861 C>A maps to NM_032184.1 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:85624861 C>A maps to NM_032184.1 L1052L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:92508476 C>T maps to NM_173567.4 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:92508476 C>T maps to NM_173567.4 R139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:109795140 C>T maps to NM_001408.2 Q814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:109795140 C>T maps to NM_001408.2 Q814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:110050943 C>T maps to NM_020703.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:110050943 C>T maps to NM_020703.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:113236731 C>T maps to NM_020963.3 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:113236731 C>T maps to NM_020963.3 I411I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:145704065 C>T maps to NM_007053.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:145704065 C>T maps to NM_007053.2 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:147090734 A>C maps to NM_004326.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:147090734 A>C maps to NM_004326.2 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:153591382 G>A maps to NM_001024210.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:153591382 G>A maps to NM_001024210.1 I95I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:154098849 C>T maps to NM_207308.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:154098849 C>T maps to NM_207308.2 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:158724676 G>A maps to NM_001005184.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:158724676 G>A maps to NM_001005184.1 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:159175723 C>A maps to NM_001122951.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:159175723 C>A maps to NM_001122951.2 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:159683845 G>A maps to NM_000567.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:159683845 G>A maps to NM_000567.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:172557993 G>T maps to ENST00000367723 E737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:172557993 G>T maps to ENST00000367723 E737*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:181767714 C>T maps to ENST00000357570 S2229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:181767714 C>T maps to ENST00000357570 S2229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:198668783 C>T maps to ENST00000271610 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:198668783 C>T maps to ENST00000271610 S130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:211280692 G>A maps to NM_172362.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:211280692 G>A maps to NM_172362.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:214816096 C>T maps to NM_016343.3 L1472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:214816096 C>T maps to NM_016343.3 L1472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:224345360 G>A maps to NM_015176.2 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:224345360 G>A maps to NM_015176.2 Q340Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:233394327 G>C maps to NM_014801.3 S427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:233394327 G>C maps to NM_014801.3 S427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:234596008 G>A maps to NM_005646.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:234596008 G>A maps to NM_005646.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:235944339 G>C maps to NM_000081.2 S1680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:235944339 G>C maps to NM_000081.2 S1680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:243579061 C>T maps to NM_006642.3 Q559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:243579061 C>T maps to NM_006642.3 Q559*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:248202315 C>T maps to NM_001004686.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr1:248202315 C>T maps to NM_001004686.2 F249F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:1070525 C>T maps to NM_033261.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:1070525 C>T maps to NM_033261.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:14995990 G>A maps to NM_001033855.1 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:14995990 G>A maps to NM_001033855.1 Q7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:34688325 G>A maps to NM_019619.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:34688325 G>A maps to NM_019619.3 L274L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:75567714 G>C maps to NM_003635.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:75567714 G>C maps to NM_003635.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:93757459 C>T maps to NM_003972.2 F1204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:93757459 C>T maps to NM_003972.2 F1204F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:94268605 G>A maps to NM_004969.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:94268605 G>A maps to NM_004969.3 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:95088618 G>A maps to NM_013451.3 Q1678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:95088618 G>A maps to NM_013451.3 Q1678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:97135750 C>T maps to NM_001034954.1 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:97135750 C>T maps to NM_001034954.1 S572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:121571449 C>T maps to NM_014937.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:121571449 C>T maps to NM_014937.2 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:124184410 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr10:124184410 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr11:397561 C>G maps to NM_007183.2 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr11:397561 C>G maps to NM_007183.2 S323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr11:5173509 C>T maps to NM_012375.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr11:5173509 C>T maps to NM_012375.2 G30G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr11:67218800 C>T maps to NM_206997.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr11:67218800 C>T maps to NM_206997.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr11:77910691 C>T maps to NM_020798.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr11:77910691 C>T maps to NM_020798.2 I286I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:304435 G>A maps to NM_003044.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:304435 G>A maps to NM_003044.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:431664 G>A maps to NM_001042603.1 R782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:431664 G>A maps to NM_001042603.1 R782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:6707088 C>T maps to ENST00000309577 W621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:6707088 C>T maps to ENST00000309577 W621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:8330154 C>T maps to NM_001004328.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:8330154 C>T maps to NM_001004328.2 F293F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:11339075 G>C maps to NM_181429.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:11339075 G>C maps to NM_181429.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:45761519 C>T maps to NM_001142679.1 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:45761519 C>T maps to NM_001142679.1 Q350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:49496667 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:49496667 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:50045025 G>A maps to NM_175736.4 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:50045025 G>A maps to NM_175736.4 F574F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:54109765 C>T maps to NM_020898.2 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:54109765 C>T maps to NM_020898.2 Q357Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:56234571 G>A maps to NM_002429.4 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:56234571 G>A maps to NM_002429.4 F133F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:62949937 C>A maps to ENST00000393630 I1126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:62949937 C>A maps to ENST00000393630 I1126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:64811847 C>T maps to NM_007235.3 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:64811847 C>T maps to NM_007235.3 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:104461750 G>A maps to NM_013320.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:104461750 G>A maps to NM_013320.2 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:113724845 C>G maps to NM_001143819.1 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:113724845 C>G maps to NM_001143819.1 L599L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:118511519 G>A maps to NM_019086.5 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:118511519 G>A maps to NM_019086.5 I401I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:121175683 G>T maps to NM_000017.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:121175683 G>T maps to NM_000017.2 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:124104569 A>G maps to NM_020936.1 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr12:124104569 A>G maps to NM_020936.1 K562K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr13:31725796 T>C maps to NM_006644.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr13:31725796 T>C maps to NM_006644.2 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr13:113980314 C>T maps to NM_024719.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr13:113980314 C>T maps to NM_024719.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:23870052 G>A maps to NM_002471.3 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:23870052 G>A maps to NM_002471.3 I425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:31578644 C>T maps to NM_015382.2 E2146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:31578644 C>T maps to NM_015382.2 E2146E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:39771448 C>G maps to ENST00000396158 Y309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:39771448 C>G maps to ENST00000396158 Y309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:57876232 G>A maps to NM_001011713.2 *363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:57876232 G>A maps to NM_001011713.2 *363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:73730415 C>T maps to ENST00000427855 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:73730415 C>T maps to ENST00000427855 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:102900645 C>T maps to NM_014844.3 Q498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr14:102900645 C>T maps to NM_014844.3 Q498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:44890481 G>A maps to NM_025137.3 Q1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:44890481 G>A maps to NM_025137.3 Q1328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:45398797 G>A maps to NM_014080.4 R625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:45398797 G>A maps to NM_014080.4 R625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:50903386 G>C maps to NM_017672.4 S728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:50903386 G>C maps to NM_017672.4 S728*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:64791778 C>G maps to NM_015042.1 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:64791778 C>G maps to NM_015042.1 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:70960835 G>C maps to NM_018003.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr15:70960835 G>C maps to NM_018003.2 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:613437 G>A maps to ENST00000293874 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:613437 G>A maps to ENST00000293874 E48E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:17202794 G>A maps to NM_022166.3 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:17202794 G>A maps to NM_022166.3 L879L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:19483457 C>T maps to NM_001105248.1 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:19483457 C>T maps to NM_001105248.1 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:22337137 C>T maps to NM_018119.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:22337137 C>T maps to NM_018119.2 Q469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:57155593 C>T maps to NM_152727.5 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:57155593 C>T maps to NM_152727.5 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:67401274 C>T maps to NM_018296.5 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:67401274 C>T maps to NM_018296.5 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:72993630 G>A maps to NM_006885.3 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:72993630 G>A maps to NM_006885.3 D138D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:75149146 G>A maps to NM_153486.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:75149146 G>A maps to NM_153486.3 I92I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:84690970 G>A maps to NM_024731.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:84690970 G>A maps to NM_024731.2 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:88744856 C>T maps to NM_178310.3 *293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr16:88744856 C>T maps to NM_178310.3 *293*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1MH-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-C5-A1MH-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:1703352 G>C maps to NM_052928.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:1703352 G>C maps to NM_052928.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:4701365 G>C maps to NM_002798.1 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:4701365 G>C maps to NM_002798.1 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:7750517 A>C maps to NM_001080424.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:7750517 A>C maps to NM_001080424.1 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:16537968 C>T maps to NM_020787.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:16537968 C>T maps to NM_020787.3 E85E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:17701148 C>T maps to ENST00000395776 S1629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:17701148 C>T maps to ENST00000395776 S1629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:27244443 C>G maps to NM_001033561.1 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:27244443 C>G maps to NM_001033561.1 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:27977721 C>T maps to NM_033389.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:27977721 C>T maps to NM_033389.2 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:38788619 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:38788619 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:42089328 G>A maps to NM_032376.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:42089328 G>A maps to NM_032376.2 F247F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:65717521 C>G maps to NM_015462.3 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:65717521 C>G maps to NM_015462.3 S114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:72436355 G>A maps to NM_022036.2 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr17:72436355 G>A maps to NM_022036.2 K192K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:9257109 C>G maps to NM_015208.3 S1282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:9257109 C>G maps to NM_015208.3 S1282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:9258685 G>A maps to NM_015208.3 E1807E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:9258685 G>A maps to NM_015208.3 E1807E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:14105523 G>A maps to NM_145287.3 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:14105523 G>A maps to NM_145287.3 Q339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:21492845 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:21492845 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:30350038 G>A maps to NM_020805.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:30350038 G>A maps to NM_020805.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:74092248 C>T maps to ENST00000443185 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr18:74092248 C>T maps to ENST00000443185 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:5135453 G>A maps to NM_015015.2 E730E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:5135453 G>A maps to NM_015015.2 E730E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:6183145 C>T maps to NM_030924.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:6183145 C>T maps to NM_030924.3 I395I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:8660995 C>T maps to NM_030957.2 W433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:8660995 C>T maps to NM_030957.2 W433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:10741982 C>T maps to NM_020428.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:10741982 C>T maps to NM_020428.3 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:11565682 C>T maps to NM_001420.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:11565682 C>T maps to NM_001420.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:38991619 C>A maps to NM_000540.2 S2535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:38991619 C>A maps to NM_000540.2 S2535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:44740721 G>A maps to NM_182490.1 E713E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:44740721 G>A maps to NM_182490.1 E713E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:46388495 C>G maps to NM_015649.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:46388495 C>G maps to NM_015649.1 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:47422774 G>C maps to NM_004491.4 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:47422774 G>C maps to NM_004491.4 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:49398375 G>C maps to NM_003323.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:49398375 G>C maps to NM_003323.2 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:49949849 G>A maps to NM_017916.2 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:49949849 G>A maps to NM_017916.2 I263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:50760688 C>G maps to NM_001145809.1 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:50760688 C>G maps to NM_001145809.1 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:56549516 C>T maps to NM_153447.4 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr19:56549516 C>T maps to NM_153447.4 L914L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:25966751 G>C maps to NM_018263.4 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:25966751 G>C maps to NM_018263.4 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:96948945 G>A maps to NM_014014.3 F1636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:96948945 G>A maps to NM_014014.3 F1636F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:100915695 G>A maps to NM_198461.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:100915695 G>A maps to NM_198461.3 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:120658343 G>A maps to NM_002830.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:120658343 G>A maps to NM_002830.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:128394376 C>G maps to ENST00000389524 L2047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:128394376 C>G maps to ENST00000389524 L2047L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:139326584 C>T maps to NM_001001664.2 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:139326584 C>T maps to NM_001001664.2 R372*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:159166126 G>A maps to NM_138803.3 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:159166126 G>A maps to NM_138803.3 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:161143485 C>G maps to NM_016836.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:161143485 C>G maps to NM_016836.3 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:179425301 A>G maps to NM_133378.4 N25951N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:179425301 A>G maps to NM_133378.4 N25951N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:179465712 C>A maps to NM_133378.4 E16072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:179465712 C>A maps to NM_133378.4 E16072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:183866921 G>A maps to NM_205842.1 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:183866921 G>A maps to NM_205842.1 R155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:191931241 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:191931241 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:201994662 C>T maps to NM_001127183.1 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:201994662 C>T maps to NM_001127183.1 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:204161617 C>G maps to ENST00000429815 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:204161617 C>G maps to ENST00000429815 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:213872481 C>A maps to ENST00000342002 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr2:213872481 C>A maps to ENST00000342002 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr20:3210346 G>C maps to NM_001174090.1 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr20:3210346 G>C maps to NM_001174090.1 S565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr20:36640988 G>A maps to NM_014657.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr20:36640988 G>A maps to NM_014657.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr20:40116319 C>G maps to NM_032221.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr20:40116319 C>G maps to NM_032221.3 L662L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr21:32598170 G>A maps to NM_003253.2 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr21:32598170 G>A maps to NM_003253.2 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr21:38525249 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr21:38525249 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr21:43411093 G>A maps to NM_020727.4 I1037I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr21:43411093 G>A maps to NM_020727.4 I1037I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr21:45211273 G>T maps to NM_003683.5 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr21:45211273 G>T maps to NM_003683.5 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr22:17072423 G>A maps to NM_014406.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr22:17072423 G>A maps to NM_014406.4 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr22:26830048 C>G maps to NM_020437.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr22:26830048 C>G maps to NM_020437.4 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr22:32756344 C>T maps to NM_001098535.1 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr22:32756344 C>T maps to NM_001098535.1 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr22:41525926 C>G maps to NM_001429.3 S401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr22:41525926 C>G maps to NM_001429.3 S401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:46716159 G>A maps to NM_147129.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:46716159 G>A maps to NM_147129.3 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:52582225 C>T maps to ENST00000296302 S1641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:52582225 C>T maps to ENST00000296302 S1641S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:99979909 C>T maps to ENST00000394144 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:99979909 C>T maps to ENST00000394144 D16D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:111886194 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:111886194 C>G did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:124374456 G>C maps to NM_001024660.3 L1934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:124374456 G>C maps to NM_001024660.3 L1934L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:130284199 C>T maps to NM_001102608.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:130284199 C>T maps to NM_001102608.1 R342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:171969134 C>A maps to NM_022763.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:171969134 C>A maps to NM_022763.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:183977944 C>T maps to NM_033259.2 *80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:183977944 C>T maps to NM_033259.2 *80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:184090792 G>A maps to NM_000460.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr3:184090792 G>A maps to NM_000460.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:16504352 C>T maps to NM_001290.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:16504352 C>T maps to NM_001290.3 A345A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:38698832 C>T maps to NM_016531.5 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:38698832 C>T maps to NM_016531.5 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:38800104 G>C maps to NM_003263.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:38800104 G>C maps to NM_003263.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:72306421 C>T maps to NM_001098484.2 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:72306421 C>T maps to NM_001098484.2 F299F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:114824077 G>A maps to NM_024590.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:114824077 G>A maps to NM_024590.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:154513679 C>G maps to NM_001131007.1 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:154513679 C>G maps to NM_001131007.1 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:170038680 C>T maps to NM_020870.3 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:170038680 C>T maps to NM_020870.3 V590V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:186274727 G>A maps to NM_031953.2 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr4:186274727 G>A maps to NM_031953.2 L688L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:13885101 G>A maps to NM_001369.2 F993F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:13885101 G>A maps to NM_001369.2 F993F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:13891183 G>A maps to NM_001369.2 F826F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:13891183 G>A maps to NM_001369.2 F826F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:35084644 G>A maps to NM_000949.4 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:35084644 G>A maps to NM_000949.4 I100I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:56219368 C>T maps to ENST00000381226 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:56219368 C>T maps to ENST00000381226 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:65077184 G>A maps to NM_020726.4 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:65077184 G>A maps to NM_020726.4 K253K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:65370982 G>A maps to ENST00000506030 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:65370982 G>A maps to ENST00000506030 L1303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:81608441 C>G maps to NM_001017971.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:81608441 C>G maps to NM_001017971.1 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:121187813 C>T maps to NM_177478.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:121187813 C>T maps to NM_177478.1 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:135583166 C>T maps to NM_020389.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:135583166 C>T maps to NM_020389.2 A612A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:140250049 C>T maps to NM_018902.3 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:140250049 C>T maps to NM_018902.3 F454F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:167674360 C>T maps to NM_001122679.1 I2130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:167674360 C>T maps to NM_001122679.1 I2130I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:173317424 C>G maps to NM_030627.2 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:173317424 C>G maps to NM_030627.2 S230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:179192493 C>G maps to NM_014757.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr5:179192493 C>G maps to NM_014757.4 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:17507542 G>A maps to NM_006366.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:17507542 G>A maps to NM_006366.2 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:32261576 C>T maps to ENST00000447241 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:32261576 C>T maps to ENST00000447241 E291E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:41658580 C>T maps to ENST00000343317 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:41658580 C>T maps to ENST00000343317 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:56394341 C>G maps to ENST00000361203 L5622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:56394341 C>G maps to ENST00000361203 L5622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:111698933 G>A maps to NM_002912.3 Q523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:111698933 G>A maps to NM_002912.3 Q523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:117244317 C>T maps to NM_173560.3 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:117244317 C>T maps to NM_173560.3 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:130761644 C>T maps to NM_052913.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:130761644 C>T maps to NM_052913.2 V26V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:158342599 G>A maps to NM_016224.3 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr6:158342599 G>A maps to NM_016224.3 E329E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:1479624 G>A maps to NM_182924.3 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:1479624 G>A maps to NM_182924.3 I634I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:2412416 G>A maps to ENST00000314800 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:2412416 G>A maps to ENST00000314800 K599K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:19739761 C>A maps to NM_001002926.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:19739761 C>A maps to NM_001002926.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:28997038 G>A maps to NM_014817.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:28997038 G>A maps to NM_014817.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:33014870 C>T maps to NM_007270.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:33014870 C>T maps to NM_007270.3 Q149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:87536721 G>A maps to NM_006716.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:87536721 G>A maps to NM_006716.3 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:100730883 G>A maps to NM_030961.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:100730883 G>A maps to NM_030961.1 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:128138113 G>A maps to NM_018396.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:128138113 G>A maps to NM_018396.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:129053477 G>A maps to NM_015328.3 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr7:129053477 G>A maps to NM_015328.3 K470K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:42552632 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:42552632 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:51569548 G>A maps to NM_018967.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:51569548 G>A maps to NM_018967.2 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:87552527 C>G maps to NM_003909.3 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:87552527 C>G maps to NM_003909.3 S200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:100133457 C>T maps to NM_017890.3 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:100133457 C>T maps to NM_017890.3 Q331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:109226921 C>T maps to NM_001568.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:109226921 C>T maps to NM_001568.2 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:144998411 C>G maps to NM_201380.2 L2032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr8:144998411 C>G maps to NM_201380.2 L2032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:14737459 C>T maps to ENST00000380880 G2161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:14737459 C>T maps to ENST00000380880 G2161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:34500822 C>G maps to NM_012144.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:34500822 C>G maps to NM_012144.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:71491607 G>C maps to NM_003558.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:71491607 G>C maps to NM_003558.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:86554521 G>A maps to NM_032307.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:86554521 G>A maps to NM_032307.3 S310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:111678516 G>A maps to NM_003640.3 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:111678516 G>A maps to NM_003640.3 Q309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:129102820 C>G maps to NM_033446.1 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:129102820 C>G maps to NM_033446.1 S39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:141010113 C>T maps to ENST00000277549 L1921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chr9:141010113 C>T maps to ENST00000277549 L1921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:23957379 C>G maps to NM_152761.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:23957379 C>G maps to NM_152761.2 S320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:32380903 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:32380903 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:55782356 G>A maps to NM_016656.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:55782356 G>A maps to NM_016656.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:62863881 C>T maps to NM_015185.2 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:62863881 C>T maps to NM_015185.2 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:90691232 C>T maps to NM_080832.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:90691232 C>T maps to NM_080832.2 F219F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:122802165 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:122802165 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:123224509 C>T maps to NM_001042750.1 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:123224509 C>T maps to NM_001042750.1 L1121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:129518527 C>T maps to NM_178471.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:129518527 C>T maps to NM_178471.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:129765490 C>T maps to NM_182314.1 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:129765490 C>T maps to NM_182314.1 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:153033711 C>T maps to NM_005393.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:153033711 C>T maps to NM_005393.2 P365P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:153763456 G>T maps to ENST00000369620 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MH-01A-11D-A14W-08 chrX:153763456 G>T maps to ENST00000369620 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:27100374 C>T maps to NM_006015.4 Q1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:27100374 C>T maps to NM_006015.4 Q1363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:116534854 C>T maps to NM_018420.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:116534854 C>T maps to NM_018420.2 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:145360623 G>A maps to NM_001039703.4 S3083S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr1:145360623 G>A maps to NM_001039703.4 S3083S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr10:46122403 G>C maps to NM_001128324.1 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr10:46122403 G>C maps to NM_001128324.1 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr10:104492658 C>T maps to NM_178858.4 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr10:104492658 C>T maps to NM_178858.4 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr10:120871422 C>T maps to NM_207009.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr10:120871422 C>T maps to NM_207009.2 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr11:63990962 G>C maps to NM_178443.2 *668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr11:63990962 G>C maps to NM_178443.2 *668S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr15:73616099 G>A maps to NM_005477.2 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr15:73616099 G>A maps to NM_005477.2 I778I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:2115599 G>T maps to NM_000548.3 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:2115599 G>T maps to NM_000548.3 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:49313389 G>A maps to NM_004352.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:49313389 G>A maps to NM_004352.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:67271210 C>T maps to NM_013241.2 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:67271210 C>T maps to NM_013241.2 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:88891255 G>A maps to NM_000512.4 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr16:88891255 G>A maps to NM_000512.4 G387G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr19:964967 G>A maps to NM_005224.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr19:964967 G>A maps to NM_005224.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr19:14516687 C>G maps to NM_078481.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr19:14516687 C>G maps to NM_078481.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr19:49652820 C>T maps to NM_003660.2 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr19:49652820 C>T maps to NM_003660.2 F1124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr2:71209787 G>A maps to NM_001115116.1 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr2:71209787 G>A maps to NM_001115116.1 Q288Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr2:73447239 G>A maps to NM_006062.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr2:73447239 G>A maps to NM_006062.2 G89G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr20:3025089 C>G maps to NM_001501.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr20:3025089 C>G maps to NM_001501.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr20:18576745 C>A maps to NM_080820.4 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr20:18576745 C>A maps to NM_080820.4 V77V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr3:12660148 G>C maps to ENST00000415519 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr3:12660148 G>C maps to ENST00000415519 G24G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr4:166976379 C>T maps to ENST00000507499 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr4:166976379 C>T maps to ENST00000507499 D582D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr5:95067757 C>G maps to NM_014899.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr5:95067757 C>G maps to NM_014899.3 V66V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr5:118865665 A>C maps to NM_000414.3 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr5:118865665 A>C maps to NM_000414.3 T615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:57467153 C>T maps to NM_000947.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:57467153 C>T maps to NM_000947.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:90312809 C>T maps to ENST00000339746 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:90312809 C>T maps to ENST00000339746 L94L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1MI-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:154567852 G>A maps to NM_001130700.1 L40L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-C5-A1MI-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:154567852 G>A maps to NM_001130700.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:170871051 G>A maps to NM_003194.4 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr6:170871051 G>A maps to NM_003194.4 Q76Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr7:72413867 G>A maps to ENST00000434423 G1112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr7:72413867 G>A maps to ENST00000434423 G1112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr7:98508770 G>A maps to ENST00000359863 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr7:98508770 G>A maps to ENST00000359863 E628E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr9:20414342 A>G maps to NM_004529.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr9:20414342 A>G maps to NM_004529.2 S167S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr9:107531249 G>A maps to NM_018376.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MI-01A-11D-A14W-08 chr9:107531249 G>A maps to NM_018376.2 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:42657385 C>T maps to NM_001198850.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:42657385 C>T maps to NM_001198850.1 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:145474434 G>A maps to NM_001039888.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:145474434 G>A maps to NM_001039888.2 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:158368641 G>T maps to NM_001004475.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:158368641 G>T maps to NM_001004475.1 I205I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:192779518 C>T maps to NM_002923.3 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:192779518 C>T maps to NM_002923.3 Q78*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:197069808 G>A maps to NM_018136.4 Q2858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:197069808 G>A maps to NM_018136.4 Q2858*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:229568793 G>A maps to NM_001100.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr1:229568793 G>A maps to NM_001100.3 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr10:124380783 C>A maps to ENST00000368915 V1832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr10:124380783 C>A maps to ENST00000368915 V1832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr10:128795092 C>T maps to ENST00000398025 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr10:128795092 C>T maps to ENST00000398025 F185F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr10:135094895 G>A maps to NM_006659.2 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr10:135094895 G>A maps to NM_006659.2 F818F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr11:94337147 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr11:94337147 A>G did not map to a codon.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr11:94731207 A>G maps to NM_018039.2 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr11:94731207 A>G maps to NM_018039.2 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr11:119185549 G>A maps to NM_006500.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr11:119185549 G>A maps to NM_006500.2 R131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr12:56436360 C>T maps to NM_001029.3 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr12:56436360 C>T maps to NM_001029.3 D52D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr13:26343348 G>A maps to NM_016529.4 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr13:26343348 G>A maps to NM_016529.4 S850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr15:28525272 C>T maps to NM_004667.4 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr15:28525272 C>T maps to NM_004667.4 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr17:19746513 G>A maps to NM_014683.3 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr17:19746513 G>A maps to NM_014683.3 Q189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr18:2937747 C>T maps to NM_014646.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr18:2937747 C>T maps to NM_014646.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr19:40513242 C>T maps to NM_178544.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr19:40513242 C>T maps to NM_178544.3 D78D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr19:58491315 A>G maps to NM_025027.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr19:58491315 A>G maps to NM_025027.3 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr2:18113429 C>T maps to NM_002252.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr2:18113429 C>T maps to NM_002252.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr2:101654035 G>A maps to NM_001102426.1 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr2:101654035 G>A maps to NM_001102426.1 T455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr2:158167844 A>G maps to NM_014568.1 K936K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr2:158167844 A>G maps to NM_014568.1 K936K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr22:50599415 G>A maps to NM_018995.2 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr22:50599415 G>A maps to NM_018995.2 L1162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr3:109027095 C>T maps to NM_138815.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr3:109027095 C>T maps to NM_138815.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr4:146435947 G>A maps to NM_001003688.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr4:146435947 G>A maps to NM_001003688.1 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr5:66398417 C>G maps to NM_001164664.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr5:66398417 C>G maps to NM_001164664.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr5:140754831 G>A maps to NM_018919.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr5:140754831 G>A maps to NM_018919.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr5:143586960 C>G maps to NM_020768.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr5:143586960 C>G maps to NM_020768.3 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr6:31864204 T>C maps to ENST00000395728 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr6:31864204 T>C maps to ENST00000395728 K196K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr7:107577712 A>G maps to NM_002291.2 I1257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr7:107577712 A>G maps to NM_002291.2 I1257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr7:122755585 C>A maps to NM_022444.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr7:122755585 C>A maps to NM_022444.3 E592*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr7:151846144 C>T maps to ENST00000355193 V4346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr7:151846144 C>T maps to ENST00000355193 V4346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr8:30657145 C>T maps to NM_001009552.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr8:30657145 C>T maps to NM_001009552.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr8:144993179 C>T maps to NM_201380.2 Q3740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr8:144993179 C>T maps to NM_201380.2 Q3740Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr9:35093899 G>A maps to NM_032634.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr9:35093899 G>A maps to NM_032634.2 I259I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr9:96062405 C>T maps to ENST00000297954 L2100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr9:96062405 C>T maps to ENST00000297954 L2100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr9:138847246 G>A maps to NM_016172.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr9:138847246 G>A maps to NM_016172.2 S51S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr9:139890113 C>T maps to NM_004669.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr9:139890113 C>T maps to NM_004669.2 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:1421178 C>T maps to NM_031921.4 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:1421178 C>T maps to NM_031921.4 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:15863293 G>T maps to NM_015291.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:15863293 G>T maps to NM_015291.2 E187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:27059193 C>T maps to NM_006015.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:27059193 C>T maps to NM_006015.4 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:38444714 G>A maps to NM_006802.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:38444714 G>A maps to NM_006802.2 L258L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:39916807 G>A maps to ENST00000361689 V4722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:39916807 G>A maps to ENST00000361689 V4722V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:41283020 C>T maps to NM_004700.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:41283020 C>T maps to NM_004700.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:94996027 C>T maps to NM_001993.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:94996027 C>T maps to NM_001993.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:114505024 C>T maps to ENST00000426820 Q761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:114505024 C>T maps to ENST00000426820 Q761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:155319337 C>T maps to ENST00000368346 K2477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:155319337 C>T maps to ENST00000368346 K2477K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:160651193 C>T maps to NM_001778.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:160651193 C>T maps to NM_001778.2 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:161166036 G>C maps to NM_005099.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:161166036 G>C maps to NM_005099.4 V338V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:201843429 C>T maps to NM_018085.4 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:201843429 C>T maps to NM_018085.4 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:202698922 G>C maps to ENST00000367264 S1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:202698922 G>C maps to ENST00000367264 S1506*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:203819760 C>T maps to NM_014827.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:203819760 C>T maps to NM_014827.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:228563769 C>T maps to NM_001098623.1 L7616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:228563769 C>T maps to NM_001098623.1 L7616L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:237947566 G>A maps to NM_001035.2 K4185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:237947566 G>A maps to NM_001035.2 K4185K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:247978611 G>C maps to NM_001001966.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:247978611 G>C maps to NM_001001966.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:26856370 C>G maps to NM_019043.3 S652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:26856370 C>G maps to NM_019043.3 S652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:70043942 C>T maps to NM_022129.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:70043942 C>T maps to NM_022129.3 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:70992571 G>A maps to NM_025130.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:70992571 G>A maps to NM_025130.3 L93L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:91195878 G>C maps to NM_213606.3 S409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:91195878 G>C maps to NM_213606.3 S409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:97380955 C>T maps to NM_002860.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:97380955 C>T maps to NM_002860.3 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:101953848 G>A maps to NM_001278.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:101953848 G>A maps to NM_001278.3 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:103990663 G>A maps to NM_005029.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:103990663 G>A maps to NM_005029.3 F172F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:103990724 G>T maps to NM_005029.3 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:103990724 G>T maps to NM_005029.3 S152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:129216660 G>A maps to ENST00000398025 E1561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr10:129216660 G>A maps to ENST00000398025 E1561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:248981 G>C maps to NM_002817.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:248981 G>C maps to NM_002817.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:1020729 C>T maps to NM_005961.2 P1198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:1020729 C>T maps to NM_005961.2 P1198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:9424907 G>C maps to NM_006391.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:9424907 G>C maps to NM_006391.2 V52V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:11398877 G>A maps to NM_198516.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:11398877 G>A maps to NM_198516.2 I276I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:16877406 G>A maps to ENST00000448080 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:16877406 G>A maps to ENST00000448080 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:17793408 C>T maps to NM_001112741.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:17793408 C>T maps to NM_001112741.1 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:47296119 G>A maps to NM_003682.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:47296119 G>A maps to NM_003682.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:61919294 C>G maps to NM_001040694.1 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:61919294 C>G maps to NM_001040694.1 L868L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:62488793 C>T maps to NM_001079559.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:62488793 C>T maps to NM_001079559.1 R528R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:65650771 C>T maps to NM_001335.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:65650771 C>T maps to NM_001335.3 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:108380359 G>A maps to NM_015065.2 I1958I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr11:108380359 G>A maps to NM_015065.2 I1958I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:56726778 G>A maps to NM_001127460.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:56726778 G>A maps to NM_001127460.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:63544013 G>A maps to NM_000706.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:63544013 G>A maps to NM_000706.3 R201R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:70954691 G>A maps to NM_001109754.1 L1397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:70954691 G>A maps to NM_001109754.1 L1397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:108942981 G>A maps to NM_014706.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:108942981 G>A maps to NM_014706.3 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:120541721 G>A maps to NM_006861.6 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr12:120541721 G>A maps to NM_006861.6 F45F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:28122531 C>T maps to NM_153371.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:28122531 C>T maps to NM_153371.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:99087953 G>A maps to NM_005766.2 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:99087953 G>A maps to NM_005766.2 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:99361908 C>G maps to NM_005073.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:99361908 C>G maps to NM_005073.3 V328V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:103257204 G>C maps to ENST00000376052 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:103257204 G>C maps to ENST00000376052 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:114469199 G>A maps to NM_182614.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr13:114469199 G>A maps to NM_182614.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr14:52735041 C>T maps to NM_000953.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr14:52735041 C>T maps to NM_000953.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:41120598 G>A maps to NM_001130143.1 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:41120598 G>A maps to NM_001130143.1 Q81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:45411370 G>C maps to NM_144565.2 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:45411370 G>C maps to NM_144565.2 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:48056111 G>A maps to NM_153618.1 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:48056111 G>A maps to NM_153618.1 E271E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:74637436 G>A maps to NM_000781.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:74637436 G>A maps to NM_000781.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:101598291 C>G maps to NM_024652.3 S1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr15:101598291 C>G maps to NM_024652.3 S1542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr16:58712777 G>A maps to NM_018231.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr16:58712777 G>A maps to NM_018231.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr16:68725653 C>T maps to NM_001793.4 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr16:68725653 C>T maps to NM_001793.4 F609F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:3989911 G>A maps to NM_015113.3 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:3989911 G>A maps to NM_015113.3 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:4576053 C>T maps to ENST00000301396 G888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:4576053 C>T maps to ENST00000301396 G888G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:4848124 A>G maps to NM_015528.1 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:4848124 A>G maps to NM_015528.1 Q289Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:7701880 A>T maps to NM_020877.2 K2802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:7701880 A>T maps to NM_020877.2 K2802*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:10360824 G>C maps to NM_017533.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:10360824 G>C maps to NM_017533.2 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:30302565 C>G maps to NM_015355.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:30302565 C>G maps to NM_015355.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:56650662 C>T maps to ENST00000240361 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:56650662 C>T maps to ENST00000240361 L1176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:79234146 G>A maps to NM_001037984.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:79234146 G>A maps to NM_001037984.1 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr18:18567071 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr18:18567071 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr18:54591289 C>T maps to NM_015285.2 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr18:54591289 C>T maps to NM_015285.2 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:581369 C>G maps to NM_001728.2 S283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:581369 C>G maps to NM_001728.2 S283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:1008172 C>T maps to NM_138690.1 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:1008172 C>T maps to NM_138690.1 L783L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:1207151 C>G maps to NM_000455.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:1207151 C>G maps to NM_000455.4 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:3762718 C>T maps to NM_172251.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:3762718 C>T maps to NM_172251.2 F7F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:11258506 C>T maps to NM_182513.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:11258506 C>T maps to NM_182513.2 G158G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:12783678 G>C maps to NM_032332.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:12783678 G>C maps to NM_032332.3 V175V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:39219658 C>T maps to NM_004924.3 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:39219658 C>T maps to NM_004924.3 I814I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:39219712 C>T maps to NM_004924.3 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:39219712 C>T maps to NM_004924.3 I832I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:39219928 G>T maps to NM_004924.3 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:39219928 G>T maps to NM_004924.3 E865*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:50168984 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:50168984 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:53269067 G>A maps to NM_198457.2 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:53269067 G>A maps to NM_198457.2 F647F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:58004284 C>G maps to NM_001098491.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr19:58004284 C>G maps to NM_001098491.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:48808939 C>T maps to NM_172311.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:48808939 C>T maps to NM_172311.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:120069237 G>C maps to NM_001017927.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:120069237 G>C maps to NM_001017927.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:127827587 G>A maps to NM_139343.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:127827587 G>A maps to NM_139343.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:141243033 G>C maps to NM_018557.2 L3101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:141243033 G>C maps to NM_018557.2 L3101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:152226591 C>T maps to NM_007115.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:152226591 C>T maps to NM_007115.3 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:172648020 G>A maps to NM_003705.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:172648020 G>A maps to NM_003705.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:179634577 G>A maps to NM_133378.4 V2910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:179634577 G>A maps to NM_133378.4 V2910V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:203155172 G>A maps to NM_015934.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:203155172 G>A maps to NM_015934.3 Q209Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:204073910 C>T maps to NM_001114132.1 Q2522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:204073910 C>T maps to NM_001114132.1 Q2522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:215645840 G>A maps to NM_000465.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr2:215645840 G>A maps to NM_000465.2 Q253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr20:30226890 C>G maps to NM_032609.2 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr20:30226890 C>G maps to NM_032609.2 S24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr20:32256039 G>C maps to NM_001024675.1 *246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr20:32256039 G>C maps to NM_001024675.1 *246S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr20:40727168 G>A maps to ENST00000373198 F1268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr20:40727168 G>A maps to ENST00000373198 F1268F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr22:36718515 G>A maps to NM_002473.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr22:36718515 G>A maps to NM_002473.4 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr22:50356424 C>G maps to NM_001001852.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr22:50356424 C>G maps to NM_001001852.3 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:52825551 C>T maps to NM_002215.2 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:52825551 C>T maps to NM_002215.2 I838I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:56766437 G>A maps to NM_001128615.1 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:56766437 G>A maps to NM_001128615.1 F384F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:58516239 G>A maps to NM_003500.3 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:58516239 G>A maps to NM_003500.3 I315I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:124837624 C>G maps to NM_001195483.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:124837624 C>G maps to NM_001195483.1 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:126139025 C>T maps to ENST00000505024 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:126139025 C>T maps to ENST00000505024 Q347*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:127642674 C>T maps to NM_207335.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:127642674 C>T maps to NM_207335.2 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:132184865 C>T maps to NM_015268.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:132184865 C>T maps to NM_015268.3 L640L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:133647581 G>A maps to NM_025041.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:133647581 G>A maps to NM_025041.2 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:141917645 C>A maps to NM_001039547.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:141917645 C>A maps to NM_001039547.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:149374820 G>A maps to NM_001168278.1 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:149374820 G>A maps to NM_001168278.1 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:152880787 C>T maps to NM_002886.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr3:152880787 C>T maps to NM_002886.2 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr4:66231718 G>A maps to NM_004439.5 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr4:66231718 G>A maps to NM_004439.5 Q661*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr4:121958174 G>A maps to NM_024574.3 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr4:121958174 G>A maps to NM_024574.3 V317V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:43659316 C>T maps to NM_182977.2 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:43659316 C>T maps to NM_182977.2 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:81573525 G>A maps to NM_001025.4 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:81573525 G>A maps to NM_001025.4 I50I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:90449159 G>A maps to NM_032119.3 L6249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:90449159 G>A maps to NM_032119.3 L6249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:140176741 G>A maps to NM_018905.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:140176741 G>A maps to NM_018905.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:171544617 G>A maps to NM_005990.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:171544617 G>A maps to NM_005990.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:180431734 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr5:180431734 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:32154455 G>A maps to NM_002586.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:32154455 G>A maps to NM_002586.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:46107442 G>A maps to NM_014936.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:46107442 G>A maps to NM_014936.4 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:143093706 G>A maps to NM_006734.3 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:143093706 G>A maps to NM_006734.3 I723I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:153077322 C>T maps to NM_003381.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:153077322 C>T maps to NM_003381.2 F130F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:154727586 C>T maps to NM_173515.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr6:154727586 C>T maps to NM_173515.2 G523G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr7:155090261 C>G maps to ENST00000344756 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr7:155090261 C>G maps to ENST00000344756 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr8:67089289 G>C maps to NM_000756.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr8:67089289 G>C maps to NM_000756.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr8:133492620 G>A maps to NM_004519.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr8:133492620 G>A maps to NM_004519.2 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr9:418176 G>A maps to NM_203447.3 L1270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr9:418176 G>A maps to NM_203447.3 L1270L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr9:1053807 C>G maps to NM_181872.4 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr9:1053807 C>G maps to NM_181872.4 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr9:101546365 C>T maps to ENST00000375018 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr9:101546365 C>T maps to ENST00000375018 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:19713766 C>T maps to NM_031892.2 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:19713766 C>T maps to NM_031892.2 E161E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:30577709 G>A maps to NM_025159.2 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:30577709 G>A maps to NM_025159.2 Q255*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:34149540 C>T maps to NM_203408.3 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:34149540 C>T maps to NM_203408.3 K285K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:49019253 G>A maps to NM_024859.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:49019253 G>A maps to NM_024859.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:53228334 G>A maps to NM_004187.3 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:53228334 G>A maps to NM_004187.3 I689I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:63488740 C>T maps to NM_017677.3 Q597Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chrX:63488740 C>T maps to NM_017677.3 Q597Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:11575525 G>C maps to NM_020780.1 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:11575525 G>C maps to NM_020780.1 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:151149167 G>T maps to ENST00000354473 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:151149167 G>T maps to ENST00000354473 L360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:155753849 C>A maps to ENST00000368331 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:155753849 C>A maps to ENST00000368331 E607*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:155755145 C>T maps to ENST00000368331 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr1:155755145 C>T maps to ENST00000368331 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr11:55904864 C>T maps to NM_001004064.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr11:55904864 C>T maps to NM_001004064.1 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr11:58919991 C>A maps to NM_198847.2 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr11:58919991 C>A maps to NM_198847.2 S284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr12:8088660 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr12:8088660 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr12:49425643 G>A maps to NM_003482.3 R4282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr12:49425643 G>A maps to NM_003482.3 R4282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr12:90036008 A>C maps to ENST00000428670 L111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr12:90036008 A>C maps to ENST00000428670 L111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr13:20763589 C>T maps to NM_004004.5 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr13:20763589 C>T maps to NM_004004.5 W44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr14:20482424 G>A maps to NM_001004712.1 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr14:20482424 G>A maps to NM_001004712.1 Q310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr14:23394234 G>A maps to NM_006109.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr14:23394234 G>A maps to NM_006109.3 F264F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr14:102793112 G>A maps to NM_018335.3 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr14:102793112 G>A maps to NM_018335.3 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr15:24923095 C>A maps to NM_018958.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr15:24923095 C>A maps to NM_018958.2 P694P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr15:89450572 G>A maps to NM_005928.2 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr15:89450572 G>A maps to NM_005928.2 N80N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr17:2139834 C>G maps to NM_017575.4 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr17:2139834 C>G maps to NM_017575.4 L940L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr17:17719222 G>A maps to NM_001005291.2 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr17:17719222 G>A maps to NM_001005291.2 S808S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr18:67781754 G>A maps to NM_173630.3 V1203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr18:67781754 G>A maps to NM_173630.3 V1203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:9068287 G>C maps to NM_024690.2 V6386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:9068287 G>C maps to NM_024690.2 V6386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:19221579 C>G maps to NM_178526.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:19221579 C>G maps to NM_178526.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:39051943 C>T maps to NM_000540.2 R4158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:39051943 C>T maps to NM_000540.2 R4158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr2:177017630 G>A maps to NM_014621.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr2:177017630 G>A maps to NM_014621.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr20:43929599 C>G maps to ENST00000372754 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr20:43929599 C>G maps to ENST00000372754 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr22:30866016 G>A maps to NM_174975.4 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr22:30866016 G>A maps to NM_174975.4 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr3:145913066 G>C maps to NM_020353.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr3:145913066 G>C maps to NM_020353.2 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr4:128554176 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr4:128554176 T>G did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr4:175414435 C>T maps to NM_000860.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr4:175414435 C>T maps to NM_000860.4 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr5:180056291 G>A maps to NM_182925.4 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr5:180056291 G>A maps to NM_182925.4 R318*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr6:16295254 T>G maps to NM_006877.3 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr6:16295254 T>G maps to NM_006877.3 T292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr6:38560592 T>C maps to NM_052893.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr6:38560592 T>C maps to NM_052893.1 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr7:142575712 G>C maps to NM_018646.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr7:142575712 G>C maps to NM_018646.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr9:21187443 G>A maps to NM_021068.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr9:21187443 G>A maps to NM_021068.2 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chrX:69353868 C>T maps to NM_001551.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chrX:69353868 C>T maps to NM_001551.2 D24D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chrX:122387319 G>A maps to NM_000828.4 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chrX:122387319 G>A maps to NM_000828.4 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:94972173 C>A maps to ENST00000454898 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:94972173 C>A maps to ENST00000454898 G631G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:118477107 C>T maps to NM_006784.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:118477107 C>T maps to NM_006784.2 Q62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:152732420 C>T maps to NM_001025231.1 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:152732420 C>T maps to NM_001025231.1 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:153660529 G>A maps to NM_000906.3 E750E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:153660529 G>A maps to NM_000906.3 E750E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:177226387 A>T maps to NM_021165.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:177226387 A>T maps to NM_021165.2 I179I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:229568026 G>A maps to NM_001100.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:229568026 G>A maps to NM_001100.3 F202F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:236716982 C>G maps to NM_018072.5 L2045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr1:236716982 C>G maps to NM_018072.5 L2045L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:18956109 G>A maps to NM_147199.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:18956109 G>A maps to NM_147199.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:58477547 C>T maps to NM_201648.2 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:58477547 C>T maps to NM_201648.2 Q194Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:62397702 C>T maps to NM_198335.2 W542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:62397702 C>T maps to NM_198335.2 W542*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:105923633 G>A maps to NM_198439.2 C594C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr11:105923633 G>A maps to NM_198439.2 C594C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr12:49438039 T>A maps to NM_003482.3 K1711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr12:49438039 T>A maps to NM_003482.3 K1711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr14:71495432 T>C maps to NM_014982.2 L1161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr14:71495432 T>C maps to NM_014982.2 L1161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr14:75266401 T>C did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr14:75266401 T>C did not map to a codon.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr15:44092973 C>T maps to NM_016400.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr15:44092973 C>T maps to NM_016400.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr15:45007718 G>T maps to NM_004048.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr15:45007718 G>T maps to NM_004048.2 E56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr15:59080148 G>A maps to NM_001040450.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr15:59080148 G>A maps to NM_001040450.1 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr16:31091076 G>A maps to NM_014699.3 P1144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr16:31091076 G>A maps to NM_014699.3 P1144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr16:67974268 G>A maps to NM_000229.1 H287H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr16:67974268 G>A maps to NM_000229.1 H287H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:1554405 G>A maps to NM_006445.3 F2283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:1554405 G>A maps to NM_006445.3 F2283F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:39537388 C>G maps to NM_021013.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:39537388 C>G maps to NM_021013.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:39596477 G>A maps to NM_006771.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:39596477 G>A maps to NM_006771.3 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:42850446 C>T maps to NM_002390.4 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:42850446 C>T maps to NM_002390.4 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:53077095 G>T maps to NM_178509.5 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:53077095 G>T maps to NM_178509.5 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:62081144 C>A maps to NM_001099789.1 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:62081144 C>A maps to NM_001099789.1 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:78318497 C>T maps to NM_020914.4 F2170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:78318497 C>T maps to NM_020914.4 F2170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:79428054 C>G maps to ENST00000436173 L2122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr17:79428054 C>G maps to ENST00000436173 L2122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr18:3729210 G>A maps to NM_004746.2 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr18:3729210 G>A maps to NM_004746.2 D505D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr18:33779771 G>C maps to NM_017947.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr18:33779771 G>C maps to NM_017947.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr19:19010502 G>A maps to NM_007263.3 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr19:19010502 G>A maps to NM_007263.3 Y304Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:18765968 C>T maps to ENST00000455492 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:18765968 C>T maps to ENST00000455492 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:74077618 C>T maps to NM_213622.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:74077618 C>T maps to NM_213622.1 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:177016483 G>A maps to NM_014621.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:177016483 G>A maps to NM_014621.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:179393093 G>A maps to NM_133378.4 R33194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:179393093 G>A maps to NM_133378.4 R33194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:209010506 G>A maps to NM_005210.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:209010506 G>A maps to NM_005210.3 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:220154977 C>T maps to NM_002846.3 V970V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:220154977 C>T maps to NM_002846.3 V970V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:220164720 G>A maps to NM_002846.3 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:220164720 G>A maps to NM_002846.3 I474I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:241535884 C>T maps to NM_023083.3 D476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr2:241535884 C>T maps to NM_023083.3 D476D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr22:30890921 C>G maps to NM_174977.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr22:30890921 C>G maps to NM_174977.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr4:39924313 G>A maps to NM_001100399.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr4:39924313 G>A maps to NM_001100399.1 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr4:173942727 C>G maps to NM_001034845.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr4:173942727 C>G maps to NM_001034845.2 L530L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr5:9122802 G>A maps to NM_003966.2 C582C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr5:9122802 G>A maps to NM_003966.2 C582C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr5:73981267 C>T maps to NM_000521.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr5:73981267 C>T maps to NM_000521.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr5:176936487 G>T maps to NM_024872.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr5:176936487 G>T maps to NM_024872.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr6:24569027 G>A maps to NM_014809.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr6:24569027 G>A maps to NM_014809.3 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr6:101312039 C>T maps to NM_006828.2 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr6:101312039 C>T maps to NM_006828.2 W47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr7:11053395 G>A maps to ENST00000303905 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr7:11053395 G>A maps to ENST00000303905 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr7:48273628 C>T maps to NM_152701.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr7:48273628 C>T maps to NM_152701.3 L260L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr7:73657530 G>A maps to NM_181471.1 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr7:73657530 G>A maps to NM_181471.1 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr8:19250841 C>G maps to NM_022071.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr8:19250841 C>G maps to NM_022071.3 L354L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr8:140630926 C>T maps to NM_016601.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chr8:140630926 C>T maps to NM_016601.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chrX:18622354 C>T maps to NM_001037343.1 N437N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chrX:18622354 C>T maps to NM_001037343.1 N437N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chrX:30712557 G>C maps to ENST00000378948 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MN-01A-11D-A14W-08 chrX:30712557 G>C maps to ENST00000378948 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:144879255 C>A maps to NM_014644.4 L1398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:144879255 C>A maps to NM_014644.4 L1398L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:144879465 C>T maps to NM_014644.4 E1328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:144879465 C>T maps to NM_014644.4 E1328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:150482444 C>T maps to ENST00000369049 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:150482444 C>T maps to ENST00000369049 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:207644372 C>A maps to NM_001006658.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:207644372 C>A maps to NM_001006658.2 L478L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:216465553 T>C maps to ENST00000366943 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr1:216465553 T>C maps to ENST00000366943 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr11:64695311 G>A maps to NM_006244.3 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr11:64695311 G>A maps to NM_006244.3 E145E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr11:68312449 C>T maps to NM_001164160.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr11:68312449 C>T maps to NM_001164160.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr13:41134583 G>C maps to NM_002015.3 Y348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr13:41134583 G>C maps to NM_002015.3 Y348*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr14:92102779 C>G maps to NM_024764.2 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr14:92102779 C>G maps to NM_024764.2 V577V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr16:74528656 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr16:74528656 C>A did not map to a codon.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr17:36485383 C>T maps to ENST00000398597 R1357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr17:36485383 C>T maps to ENST00000398597 R1357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr17:61882429 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr17:61882429 G>C did not map to a codon.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr2:26257497 C>T maps to NM_016131.4 D7D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr2:26257497 C>T maps to NM_016131.4 D7D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:49051890 C>G maps to NM_018031.3 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:49051890 C>G maps to NM_018031.3 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:49053408 C>T maps to NM_001009996.1 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:49053408 C>T maps to NM_001009996.1 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:49201116 G>A maps to NM_022903.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:49201116 G>A maps to NM_022903.3 L175L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:140401672 C>T maps to NM_152616.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:140401672 C>T maps to NM_152616.4 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:186940920 C>T maps to NM_001879.5 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr3:186940920 C>T maps to NM_001879.5 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr4:156716530 G>T maps to ENST00000502959 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr4:156716530 G>T maps to ENST00000502959 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr4:186180182 C>T maps to NM_031953.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr4:186180182 C>T maps to NM_031953.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr6:17800191 C>T maps to NM_022113.4 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr6:17800191 C>T maps to NM_022113.4 L869L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chrX:91132648 C>T maps to NM_032968.3 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chrX:91132648 C>T maps to NM_032968.3 F470F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr13:77460013 G>A maps to NM_138444.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr13:77460013 G>A maps to NM_138444.3 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr14:105684014 G>A maps to NM_001519.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr14:105684014 G>A maps to NM_001519.2 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr15:32926202 G>A maps to NM_014783.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr15:32926202 G>A maps to NM_014783.3 L435L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr17:10541419 G>A maps to NM_002470.2 S1223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr17:10541419 G>A maps to NM_002470.2 S1223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:3595525 G>A maps to NM_002936.3 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:3595525 G>A maps to NM_002936.3 Q257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27276035 G>A maps to NM_021831.5 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27276035 G>A maps to NM_021831.5 G70G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27276871 G>T maps to NM_021831.5 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27276871 G>T maps to NM_021831.5 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27278088 G>A maps to NM_021831.5 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27278088 G>A maps to NM_021831.5 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27278588 G>A maps to NM_021831.5 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27278588 G>A maps to NM_021831.5 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr20:57899465 C>T maps to NM_207034.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr20:57899465 C>T maps to NM_207034.1 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr22:31535959 C>T maps to NM_015715.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr22:31535959 C>T maps to NM_015715.3 G127G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr3:49002354 C>G maps to NM_006321.2 Y109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr3:49002354 C>G maps to NM_006321.2 Y109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr3:52821210 G>A maps to NM_002215.2 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr3:52821210 G>A maps to NM_002215.2 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr3:126736416 C>T maps to NM_032242.3 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr3:126736416 C>T maps to NM_032242.3 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr4:5620290 G>A maps to NM_147127.4 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr4:5620290 G>A maps to NM_147127.4 R874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr4:85699804 G>A maps to NM_014991.4 L1457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr4:85699804 G>A maps to NM_014991.4 L1457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr5:56205484 C>T maps to NM_153706.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr5:56205484 C>T maps to NM_153706.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr5:156770010 G>A maps to NM_001001343.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr5:156770010 G>A maps to NM_001001343.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr5:180669215 G>C maps to NM_006098.4 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr5:180669215 G>C maps to NM_006098.4 S80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr6:37611648 G>A maps to ENST00000297153 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr6:37611648 G>A maps to ENST00000297153 L827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr7:883119 C>T maps to ENST00000456758 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr7:883119 C>T maps to ENST00000456758 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr7:2952969 C>T maps to NM_032415.4 Q990Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr7:2952969 C>T maps to NM_032415.4 Q990Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr7:99695254 G>A maps to NM_005916.3 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr7:99695254 G>A maps to NM_005916.3 R367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr10:108432646 T>C maps to NM_001013031.1 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr10:108432646 T>C maps to NM_001013031.1 R679R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr10:111881893 A>G maps to NM_016824.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr10:111881893 A>G maps to NM_016824.3 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr11:22849395 C>A maps to NM_148893.1 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr11:22849395 C>A maps to NM_148893.1 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr12:48528575 C>T maps to NM_001166686.1 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr12:48528575 C>T maps to NM_001166686.1 D308D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr12:53824965 T>C maps to NM_020547.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr12:53824965 T>C maps to NM_020547.2 P477P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr13:101728268 G>A maps to NM_052867.2 G1303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr13:101728268 G>A maps to NM_052867.2 G1303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr16:4383432 A>G maps to NM_032575.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr16:4383432 A>G maps to NM_032575.2 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr16:22122306 C>T maps to NM_173615.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr16:22122306 C>T maps to NM_173615.3 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr17:28434999 T>C maps to NM_198529.3 Y1490Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr17:28434999 T>C maps to NM_198529.3 Y1490Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr17:62290373 G>A maps to NM_018469.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr17:62290373 G>A maps to NM_018469.3 L402L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr19:3964676 G>A maps to NM_001348.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr19:3964676 G>A maps to NM_001348.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr19:23544538 A>T maps to NM_003430.2 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr19:23544538 A>T maps to NM_003430.2 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr4:122835997 C>A maps to NM_001130698.1 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr4:122835997 C>A maps to NM_001130698.1 V426V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr5:15936808 C>T maps to NM_012304.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr5:15936808 C>T maps to NM_012304.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr5:140230161 G>T maps to NM_031857.1 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr5:140230161 G>T maps to NM_031857.1 V694V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr6:27101230 G>T maps to NM_021064.4 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr6:27101230 G>T maps to NM_021064.4 A127A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr6:27841105 C>T maps to NM_003546.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr6:27841105 C>T maps to NM_003546.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr7:56122147 C>G maps to NM_001762.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr7:56122147 C>G maps to NM_001762.3 V96V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chrX:30686130 G>A maps to ENST00000378948 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chrX:30686130 G>A maps to ENST00000378948 W52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chrX:114082599 C>T maps to NM_000868.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chrX:114082599 C>T maps to NM_000868.2 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chrX:136649492 C>T maps to NM_003413.3 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chrX:136649492 C>T maps to NM_003413.3 Q215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:861389 G>C maps to ENST00000443100 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:861389 G>C maps to ENST00000443100 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:1203342 C>T maps to NM_194315.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:1203342 C>T maps to NM_194315.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:2445806 C>T maps to ENST00000425477 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:2445806 C>T maps to ENST00000425477 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:3427461 G>A maps to ENST00000452816 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:3427461 G>A maps to ENST00000452816 V448V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:6214951 G>C maps to NM_015557.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:6214951 G>C maps to NM_015557.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:8426004 C>T maps to NM_012102.3 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:8426004 C>T maps to NM_012102.3 W438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:11855207 C>T maps to ENST00000376585 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:11855207 C>T maps to ENST00000376585 E367E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:12009903 G>A maps to ENST00000376369 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:12009903 G>A maps to ENST00000376369 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:16257905 C>G maps to NM_015001.2 S1724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:16257905 C>G maps to NM_015001.2 S1724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:16907342 C>T maps to NM_017940.3 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:16907342 C>T maps to NM_017940.3 K496K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:22159061 C>T maps to NM_005529.5 G3711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:22159061 C>T maps to NM_005529.5 G3711G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:26752836 C>G maps to NM_024674.4 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:26752836 C>G maps to NM_024674.4 S173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:27092808 C>T maps to NM_006015.4 Q944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:27092808 C>T maps to NM_006015.4 Q944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:27428976 G>C maps to NM_003047.3 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:27428976 G>C maps to NM_003047.3 L573L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:27440752 G>C maps to NM_003047.3 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:27440752 G>C maps to NM_003047.3 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:38019728 G>C maps to NM_024700.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:38019728 G>C maps to NM_024700.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:47571829 G>A maps to NM_178134.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:47571829 G>A maps to NM_178134.2 T366T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:52861943 G>A maps to NM_004153.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:52861943 G>A maps to NM_004153.3 F165F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:54371904 C>T maps to NM_000792.5 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:54371904 C>T maps to NM_000792.5 Q207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:55277498 G>A maps to NM_001110533.1 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:55277498 G>A maps to NM_001110533.1 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:57480997 C>T maps to ENST00000371231 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:57480997 C>T maps to ENST00000371231 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:65332605 G>A maps to NM_002227.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:65332605 G>A maps to NM_002227.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:94337711 G>C maps to NM_014597.4 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:94337711 G>C maps to NM_014597.4 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:110882686 G>A maps to NM_022768.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:110882686 G>A maps to NM_022768.4 V220V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:116929995 C>T maps to NM_000701.7 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:116929995 C>T maps to NM_000701.7 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:116931551 C>G maps to NM_000701.7 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:116931551 C>G maps to NM_000701.7 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:117626691 G>A maps to NM_003594.3 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:117626691 G>A maps to NM_003594.3 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:118482164 G>A maps to NM_006784.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:118482164 G>A maps to NM_006784.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:118491032 G>A maps to NM_006784.2 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:118491032 G>A maps to NM_006784.2 G476G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:150082609 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:150082609 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:150671182 G>A maps to NM_032132.4 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:150671182 G>A maps to NM_032132.4 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:151204208 G>C maps to NM_001135638.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:151204208 G>C maps to NM_001135638.1 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:151206944 C>T maps to NM_001135638.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:151206944 C>T maps to NM_001135638.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:151824758 G>C maps to NM_182578.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:151824758 G>C maps to NM_182578.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:152382128 C>A maps to NM_016190.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:152382128 C>A maps to NM_016190.2 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:153713819 C>T maps to ENST00000428986 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:153713819 C>T maps to ENST00000428986 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:153742318 C>G maps to ENST00000428986 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:153742318 C>G maps to ENST00000428986 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:154187020 G>C maps to NM_001098616.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:154187020 G>C maps to NM_001098616.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:154543730 C>T maps to NM_000748.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:154543730 C>T maps to NM_000748.2 F144F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:154744506 G>A maps to NM_002249.4 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:154744506 G>A maps to NM_002249.4 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:155695198 G>C maps to NM_004632.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:155695198 G>C maps to NM_004632.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:155934785 G>A maps to NM_001162383.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:155934785 G>A maps to NM_001162383.1 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:155988143 C>T maps to ENST00000368312 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:155988143 C>T maps to ENST00000368312 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:157737270 G>C maps to NM_030764.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:157737270 G>C maps to NM_030764.3 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:158390316 G>A maps to NM_001004476.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:158390316 G>A maps to NM_001004476.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:158549182 G>A maps to NM_001004477.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:158549182 G>A maps to NM_001004477.1 F169F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:162353430 C>G maps to NM_001135240.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:162353430 C>G maps to NM_001135240.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:162546700 C>T maps to ENST00000367925 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:162546700 C>T maps to ENST00000367925 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:162560262 C>T maps to ENST00000367925 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:162560262 C>T maps to ENST00000367925 F440F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:165173198 G>C maps to NM_177398.3 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:165173198 G>C maps to NM_177398.3 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:165514073 C>T maps to NM_001005214.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:165514073 C>T maps to NM_001005214.3 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:167097843 G>C maps to NM_001080426.1 *1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:167097843 G>C maps to NM_001080426.1 *1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:167301705 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:167301705 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:175067645 G>C maps to NM_022093.1 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:175067645 G>C maps to NM_022093.1 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:176640120 G>A maps to NM_020318.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:176640120 G>A maps to NM_020318.2 V669V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:197396582 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:197396582 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:208383783 G>A maps to NM_025179.3 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:208383783 G>A maps to NM_025179.3 F404F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:210015686 C>G maps to NM_014388.6 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:210015686 C>G maps to NM_014388.6 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:210015735 C>T maps to NM_014388.6 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:210015735 C>T maps to NM_014388.6 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:228469877 C>G maps to NM_001098623.1 L2814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:228469877 C>G maps to NM_001098623.1 L2814L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:229730241 C>T maps to NM_014409.3 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:229730241 C>T maps to NM_014409.3 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:231830493 C>T maps to NM_001164537.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:231830493 C>T maps to NM_001164537.1 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:237872192 C>T maps to NM_001035.2 Q3313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:237872192 C>T maps to NM_001035.2 Q3313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:241714341 C>T maps to NM_003679.3 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:241714341 C>T maps to NM_003679.3 Q104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:244735746 C>T maps to NM_001130957.1 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:244735746 C>T maps to NM_001130957.1 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:248616298 C>G maps to NM_001004136.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:248616298 C>G maps to NM_001004136.1 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:17636382 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:17636382 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:27454083 C>T maps to NM_001172303.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:27454083 C>T maps to NM_001172303.1 I215I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:28283894 C>T maps to NM_018076.2 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:28283894 C>T maps to NM_018076.2 W59*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:45924145 C>T maps to NM_000698.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:45924145 C>T maps to NM_000698.2 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:55698579 G>C maps to NM_001142763.1 S1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:55698579 G>C maps to NM_001142763.1 S1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:75553452 C>T maps to NM_015037.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:75553452 C>T maps to NM_015037.2 L807L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:76788622 C>T maps to NM_012330.2 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:76788622 C>T maps to NM_012330.2 L1347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:76979067 C>T maps to NM_001184783.1 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:76979067 C>T maps to NM_001184783.1 Q119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:90427328 C>T maps to NM_001198829.1 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:90427328 C>T maps to NM_001198829.1 Q47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:98405364 C>A maps to NM_152309.2 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:98405364 C>A maps to NM_152309.2 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:101639881 C>A maps to ENST00000342239 E1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:101639881 C>A maps to ENST00000342239 E1436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:112838143 C>G maps to NM_000681.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:112838143 C>G maps to NM_000681.3 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:112839031 C>T maps to NM_000681.3 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:112839031 C>T maps to NM_000681.3 F426F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:116048874 C>T maps to NM_198496.1 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:116048874 C>T maps to NM_198496.1 F583F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:119805359 G>C maps to ENST00000369199 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:119805359 G>C maps to ENST00000369199 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:121569691 C>G maps to NM_014937.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:121569691 C>G maps to NM_014937.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:124348772 C>T maps to ENST00000368915 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:124348772 C>T maps to ENST00000368915 V699V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:127542655 G>C maps to NM_018180.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:127542655 G>C maps to NM_018180.2 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:135112975 C>T maps to NM_006659.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:135112975 C>T maps to NM_006659.2 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:606579 C>G maps to ENST00000264555 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:606579 C>G maps to ENST00000264555 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:607351 C>T maps to ENST00000264555 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:607351 C>T maps to ENST00000264555 F632F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:1028328 G>A maps to NM_005961.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:1028328 G>A maps to NM_005961.2 I550I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:1028942 G>A maps to NM_005961.2 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:1028942 G>A maps to NM_005961.2 Q467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:17793717 C>T maps to NM_001112741.1 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:17793717 C>T maps to NM_001112741.1 F359F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:31312393 G>A maps to NM_181807.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:31312393 G>A maps to NM_181807.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:34472556 C>T maps to NM_001752.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:34472556 C>T maps to NM_001752.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:57472621 C>T maps to ENST00000431606 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:57472621 C>T maps to ENST00000431606 K99K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:63990555 C>T maps to NM_178443.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:63990555 C>T maps to NM_178443.2 I573I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:64609202 G>A maps to NM_017525.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:64609202 G>A maps to NM_017525.2 V85V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:65349986 C>G maps to NM_001099409.1 S615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:65349986 C>G maps to NM_001099409.1 S615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:66467040 G>C maps to NM_006946.2 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:66467040 G>C maps to NM_006946.2 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:67044811 G>A maps to NM_001619.3 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:67044811 G>A maps to NM_001619.3 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:67353984 C>G maps to NM_000852.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:67353984 C>G maps to NM_000852.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:68125244 G>T maps to NM_002335.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:68125244 G>T maps to NM_002335.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:68512460 G>C maps to NM_004923.3 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:68512460 G>C maps to NM_004923.3 S250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:70333106 C>T maps to ENST00000338508 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:70333106 C>T maps to ENST00000338508 R1091R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:71903283 C>T maps to NM_016729.2 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:71903283 C>T maps to NM_016729.2 Q23*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:71903324 C>G maps to NM_016729.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:71903324 C>G maps to NM_016729.2 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:72408142 G>C maps to NM_001040118.2 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:72408142 G>C maps to NM_001040118.2 L1017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:72533172 G>A maps to NM_033388.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:72533172 G>A maps to NM_033388.1 Q159Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:113230726 G>A maps to NM_017868.3 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:113230726 G>A maps to NM_017868.3 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:114320604 C>T maps to NM_015523.3 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:114320604 C>T maps to NM_015523.3 Q208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:116692247 G>A maps to NM_000482.3 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:116692247 G>A maps to NM_000482.3 Q176*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:118940947 C>T maps to NM_021729.4 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:118940947 C>T maps to NM_021729.4 F158F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:119053982 C>A maps to NM_024618.2 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:119053982 C>A maps to NM_024618.2 L921L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:119207070 C>T maps to NM_032015.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:119207070 C>T maps to NM_032015.3 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:120776192 G>C maps to NM_014619.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:120776192 G>C maps to NM_014619.2 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:123676286 C>T maps to NM_001005325.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:123676286 C>T maps to NM_001005325.1 V257V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:123813597 C>T maps to NM_001005187.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:123813597 C>T maps to NM_001005187.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:134027949 C>A maps to NM_015261.2 L1349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:134027949 C>A maps to NM_015261.2 L1349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:134047137 G>A maps to NM_015261.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr11:134047137 G>A maps to NM_015261.2 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:2719825 C>T maps to NM_199460.2 F1246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:2719825 C>T maps to NM_199460.2 F1246F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:2908401 C>G maps to NM_002014.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:2908401 C>G maps to NM_002014.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:6782422 C>T maps to NM_001135734.1 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:6782422 C>T maps to NM_001135734.1 E290E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:11174552 G>C maps to NM_176888.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:11174552 G>C maps to NM_176888.1 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:21790115 G>A maps to NM_002300.6 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:21790115 G>A maps to NM_002300.6 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:31244670 C>T maps to NM_030653.3 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:31244670 C>T maps to NM_030653.3 Q370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:40040239 C>G maps to NM_001031748.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:40040239 C>G maps to NM_001031748.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:49425637 G>A maps to NM_003482.3 Q4284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:49425637 G>A maps to NM_003482.3 Q4284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:51458155 C>T maps to NM_030809.1 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:51458155 C>T maps to NM_030809.1 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:52940164 C>T maps to NM_033448.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:52940164 C>T maps to NM_033448.2 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:53700809 G>C maps to NM_021640.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:53700809 G>C maps to NM_021640.3 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:56815234 G>C maps to NM_003920.3 S923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:56815234 G>C maps to NM_003920.3 S923*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:56994156 G>A maps to NM_013449.3 Q1576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:56994156 G>A maps to NM_013449.3 Q1576*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:57107410 C>T maps to NM_001113203.1 R1960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:57107410 C>T maps to NM_001113203.1 R1960R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:85459080 C>G maps to NM_001079910.1 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:85459080 C>G maps to NM_001079910.1 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:91539882 G>A maps to NM_133503.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:91539882 G>A maps to NM_133503.2 F344F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:97150282 C>T maps to ENST00000342887 Q1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:97150282 C>T maps to ENST00000342887 Q1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:104131461 C>T maps to NM_017564.9 L1867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:104131461 C>T maps to NM_017564.9 L1867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:107391156 C>G maps to NM_004075.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:107391156 C>G maps to NM_004075.3 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:112119639 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:112119639 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:113714773 C>T maps to NM_001143819.1 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:113714773 C>T maps to NM_001143819.1 F403F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:120575380 C>A maps to NM_006836.1 E2211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:120575380 C>A maps to NM_006836.1 E2211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:120800869 C>T maps to NM_002442.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:120800869 C>T maps to NM_002442.2 K126K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:123058850 C>G maps to NM_014708.4 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:123058850 C>G maps to NM_014708.4 S769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:124158263 C>T maps to NM_024809.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:124158263 C>T maps to NM_024809.3 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:26959423 C>T maps to NM_001260.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:26959423 C>T maps to NM_001260.1 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:29286974 G>C maps to NM_001135919.1 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:29286974 G>C maps to NM_001135919.1 S301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:42876456 C>G maps to NM_016248.2 S1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:42876456 C>G maps to NM_016248.2 S1192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:46935610 G>A maps to NM_025113.2 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:46935610 G>A maps to NM_025113.2 Q362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:47286682 C>T maps to NM_001164211.1 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:47286682 C>T maps to NM_001164211.1 V535V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:52348139 G>A maps to NM_001031719.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:52348139 G>A maps to NM_001031719.1 Q132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:52667253 G>A maps to NM_199289.1 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:52667253 G>A maps to NM_199289.1 Q382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:84454214 G>T maps to NM_052910.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:84454214 G>T maps to NM_052910.1 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:111927124 C>T maps to NM_001113511.1 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr13:111927124 C>T maps to NM_001113511.1 F441F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:20944589 C>T maps to NM_000270.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:20944589 C>T maps to NM_000270.3 R234*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:23844998 G>A maps to NM_022789.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:23844998 G>A maps to NM_022789.3 E148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:38724387 C>T maps to NM_175060.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:38724387 C>T maps to NM_175060.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:42361084 C>G maps to NM_152447.3 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:42361084 C>G maps to NM_152447.3 S673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:45564748 C>T maps to NM_017922.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:45564748 C>T maps to NM_017922.3 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:51054633 C>G maps to ENST00000358385 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:51054633 C>G maps to ENST00000358385 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:51404507 C>T maps to NM_002863.4 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:51404507 C>T maps to NM_002863.4 Q97Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:55621363 C>T maps to NM_014750.4 K678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:55621363 C>T maps to NM_014750.4 K678K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:57938126 C>T maps to NM_018168.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:57938126 C>T maps to NM_018168.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:58832748 C>T maps to NM_002892.3 S1108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:58832748 C>T maps to NM_002892.3 S1108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:59782053 C>G maps to NM_014992.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:59782053 C>G maps to NM_014992.1 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:67799666 G>A maps to NM_022474.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:67799666 G>A maps to NM_022474.2 L674L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:68257343 C>A maps to NM_015346.3 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:68257343 C>A maps to NM_015346.3 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:69262693 C>G maps to NM_207442.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:69262693 C>G maps to NM_207442.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:88983587 G>A maps to NM_007039.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:88983587 G>A maps to NM_007039.3 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:91931635 C>T maps to ENST00000417249 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:91931635 C>T maps to ENST00000417249 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:93396081 C>T maps to NM_001275.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:93396081 C>T maps to NM_001275.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:94038401 C>T maps to ENST00000393153 Q640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:94038401 C>T maps to ENST00000393153 Q640*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:94545829 C>A maps to NM_020414.3 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:94545829 C>A maps to NM_020414.3 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:96864439 C>A maps to NM_152327.2 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:96864439 C>A maps to NM_152327.2 S45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:105643315 C>T maps to NM_177533.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:105643315 C>T maps to NM_177533.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:33988602 C>T maps to NM_001036.3 I2015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:33988602 C>T maps to NM_001036.3 I2015I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:35166069 G>A maps to NM_014691.2 Q1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:35166069 G>A maps to NM_014691.2 Q1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:40764158 G>A maps to NM_130468.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:40764158 G>A maps to NM_130468.3 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:41275975 G>A maps to NM_017553.1 V1407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:41275975 G>A maps to NM_017553.1 V1407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:42446304 G>A maps to ENST00000397272 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:42446304 G>A maps to ENST00000397272 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:42731631 C>T maps to NM_022473.1 K1358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:42731631 C>T maps to NM_022473.1 K1358K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:43658611 C>T maps to NM_152455.3 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:43658611 C>T maps to NM_152455.3 Q306Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:43814639 C>G maps to ENST00000382031 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:43814639 C>G maps to ENST00000382031 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:49048134 G>A maps to NM_001194998.1 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:49048134 G>A maps to NM_001194998.1 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:49064852 G>C maps to NM_001194998.1 S538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:49064852 G>C maps to NM_001194998.1 S538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:50190328 C>T maps to NM_024837.2 K803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:50190328 C>T maps to NM_024837.2 K803K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:52090410 G>A maps to NM_014548.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:52090410 G>A maps to NM_014548.3 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:52901376 C>T maps to NM_019600.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:52901376 C>T maps to NM_019600.2 L578L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:64701922 G>A maps to NM_016213.4 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:64701922 G>A maps to NM_016213.4 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:67664959 C>G maps to NM_001031715.2 S422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:67664959 C>G maps to NM_001031715.2 S422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:73415040 C>T maps to NM_002499.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:73415040 C>T maps to NM_002499.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:74474748 G>A maps to ENST00000449139 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:74474748 G>A maps to ENST00000449139 F490F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:75980336 G>T maps to NM_001897.4 I1023I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:75980336 G>T maps to NM_001897.4 I1023I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:78775676 G>C maps to NM_004136.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:78775676 G>C maps to NM_004136.2 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:82533677 G>C maps to NM_024580.5 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:82533677 G>C maps to NM_024580.5 S104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:89391201 C>T maps to NM_013227.3 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:89391201 C>T maps to NM_013227.3 V555V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:90349433 G>A maps to NM_001150.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:90349433 G>A maps to NM_001150.2 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:92459365 G>C maps to NM_013272.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr15:92459365 G>C maps to NM_013272.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:1591970 C>A maps to NM_024600.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:1591970 C>A maps to NM_024600.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:1715110 C>T maps to NM_020825.3 F908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:1715110 C>T maps to NM_020825.3 F908F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:3433400 G>C maps to ENST00000396852 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:3433400 G>C maps to ENST00000396852 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:4016741 C>T maps to NM_001116.3 L1032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:4016741 C>T maps to NM_001116.3 L1032L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:16255324 G>C maps to NM_001171.5 L1201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:16255324 G>C maps to NM_001171.5 L1201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:16282744 G>C maps to NM_001171.5 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:16282744 G>C maps to NM_001171.5 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:28192331 G>C maps to NM_015171.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:28192331 G>C maps to NM_015171.2 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:31733960 C>T maps to NM_001130913.1 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:31733960 C>T maps to NM_001130913.1 F6F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:49433131 C>G maps to NM_144602.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:49433131 C>G maps to NM_144602.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:56918015 C>T maps to NM_000339.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:56918015 C>T maps to NM_000339.2 I575I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:57503909 G>C maps to NM_032940.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:57503909 G>C maps to NM_032940.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:57601500 C>T maps to ENST00000349457 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:57601500 C>T maps to ENST00000349457 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:57789805 C>T maps to NM_005886.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:57789805 C>T maps to NM_005886.2 L540L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:58768069 G>A maps to NM_002080.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:58768069 G>A maps to NM_002080.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:67974262 G>A maps to NM_000229.1 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:67974262 G>A maps to NM_000229.1 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:67974358 G>A maps to NM_000229.1 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:67974358 G>A maps to NM_000229.1 I257I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:68090293 C>G maps to NM_017803.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:68090293 C>G maps to NM_017803.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:69776285 C>G maps to NM_014062.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:69776285 C>G maps to NM_014062.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:71015348 C>T maps to NM_032821.2 L1484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:71015348 C>T maps to NM_032821.2 L1484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:85689361 G>A maps to NM_014615.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:85689361 G>A maps to NM_014615.2 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:88878027 G>A maps to NM_000485.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:88878027 G>A maps to NM_000485.2 F39F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:89724710 G>A maps to NM_153025.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:89724710 G>A maps to NM_153025.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:90001668 C>T maps to ENST00000304984 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr16:90001668 C>T maps to ENST00000304984 F617F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:643788 C>T maps to NM_024792.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:643788 C>T maps to NM_024792.1 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:2195914 C>T maps to NM_017575.4 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:2195914 C>T maps to NM_017575.4 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:2596109 C>G maps to NM_015229.3 V1053V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:2596109 C>G maps to NM_015229.3 V1053V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:3559813 G>C maps to NM_001031681.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:3559813 G>C maps to NM_001031681.2 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:4711669 C>T maps to NM_002663.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:4711669 C>T maps to NM_002663.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:5364390 G>A maps to ENST00000457531 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:5364390 G>A maps to ENST00000457531 F298F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7123963 C>G maps to ENST00000356839 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7123963 C>G maps to ENST00000356839 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7125394 G>A maps to ENST00000356839 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7125394 G>A maps to ENST00000356839 W295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7196798 G>T maps to NM_015982.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7196798 G>T maps to NM_015982.3 I110I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7481233 G>A maps to NM_001416.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7481233 G>A maps to NM_001416.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7674069 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:7674069 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:13977715 C>G maps to NM_001303.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:13977715 C>G maps to NM_001303.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:15449100 G>A maps to NM_145301.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:15449100 G>A maps to NM_145301.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:16021222 G>A maps to ENST00000395857 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:16021222 G>A maps to ENST00000395857 L678L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:26108114 G>A maps to NM_000625.4 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:26108114 G>A maps to NM_000625.4 Q271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:27064451 C>T maps to NM_178170.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:27064451 C>T maps to NM_178170.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:27939912 C>T maps to NM_152345.4 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:27939912 C>T maps to NM_152345.4 I528I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:29663831 C>T maps to NM_001042492.2 F2109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:29663831 C>T maps to NM_001042492.2 F2109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:35346677 C>T maps to NM_012138.3 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:35346677 C>T maps to NM_012138.3 Q428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:39969495 C>T maps to NM_021939.3 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:39969495 C>T maps to NM_021939.3 N70N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:45918125 G>A maps to NM_138355.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:45918125 G>A maps to NM_138355.3 I28I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:46052531 C>G maps to NM_176096.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:46052531 C>G maps to NM_176096.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:46135814 C>G maps to ENST00000362042 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:46135814 C>G maps to ENST00000362042 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:57889098 C>T maps to NM_030938.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:57889098 C>T maps to NM_030938.3 F288F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:59489401 C>G maps to NM_203425.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:59489401 C>G maps to NM_203425.1 L22L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:59958413 G>C maps to NM_020748.2 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:59958413 G>C maps to NM_020748.2 L744L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:66040015 G>A maps to NM_002266.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:66040015 G>A maps to NM_002266.2 V331V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:66538871 C>T maps to NM_017565.3 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:66538871 C>T maps to NM_017565.3 K297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:72921681 C>T maps to NM_178160.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:72921681 C>T maps to NM_178160.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:73552125 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:73552125 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:73738842 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:73738842 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:74072989 C>G maps to NM_003857.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:74072989 C>G maps to NM_003857.2 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:74276385 G>A maps to NM_032134.1 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:74276385 G>A maps to NM_032134.1 L1370L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:74570584 G>A maps to NM_006456.2 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:74570584 G>A maps to NM_006456.2 Q75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:74625171 C>T maps to NM_018414.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:74625171 C>T maps to NM_018414.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:76394391 C>G maps to NM_024419.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:76394391 C>G maps to NM_024419.3 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:76394406 C>G maps to NM_024419.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:76394406 C>G maps to NM_024419.3 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:76993302 C>G maps to NM_138793.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:76993302 C>G maps to NM_138793.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:78180857 C>T maps to NM_024110.2 V927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:78180857 C>T maps to NM_024110.2 V927V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:78328271 C>T maps to NM_020914.4 L3635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:78328271 C>T maps to NM_020914.4 L3635L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:8394575 G>A maps to NM_001105244.1 L1437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:8394575 G>A maps to NM_001105244.1 L1437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:21134843 C>T maps to NM_000271.4 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:21134843 C>T maps to NM_000271.4 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:25583080 G>T maps to NM_001792.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:25583080 G>T maps to NM_001792.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:29046628 G>A maps to NM_001944.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:29046628 G>A maps to NM_001944.2 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:43450594 C>T maps to NM_020964.2 T2054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:43450594 C>T maps to NM_020964.2 T2054T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:43467828 G>A maps to NM_020964.2 Q1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:43467828 G>A maps to NM_020964.2 Q1666*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:44555157 G>C maps to NM_145653.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:44555157 G>C maps to NM_145653.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:77895866 G>A maps to NM_014913.3 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr18:77895866 G>A maps to NM_014913.3 V857V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:881595 G>C maps to NM_005481.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:881595 G>C maps to NM_005481.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:2226836 C>T maps to ENST00000221482 L1439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:2226836 C>T maps to ENST00000221482 L1439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:3576257 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:3576257 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:7550777 G>C maps to NM_080662.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:7550777 G>C maps to NM_080662.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:7689277 G>A maps to NM_020196.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:7689277 G>A maps to NM_020196.2 F292F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:7795303 G>A maps to NM_198492.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:7795303 G>A maps to NM_198492.3 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:9071869 C>T maps to NM_024690.2 L5192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:9071869 C>T maps to NM_024690.2 L5192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:11034791 C>T maps to NM_024029.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:11034791 C>T maps to NM_024029.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:12155222 C>T maps to NM_001080404.1 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:12155222 C>T maps to NM_001080404.1 K378K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:14262962 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:14262962 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:15852819 C>T maps to NM_013938.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:15852819 C>T maps to NM_013938.1 V206V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:15853002 C>A maps to NM_013938.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:15853002 C>A maps to NM_013938.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:15918292 C>T maps to NM_013940.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:15918292 C>T maps to NM_013940.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:17444511 C>T maps to NM_020959.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:17444511 C>T maps to NM_020959.2 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:18731228 G>A maps to NM_012109.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:18731228 G>A maps to NM_012109.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:36104781 G>A maps to NM_015302.1 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:36104781 G>A maps to NM_015302.1 K58K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:36258751 G>A maps to NM_001039887.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:36258751 G>A maps to NM_001039887.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:39306253 C>T maps to NM_001398.2 *329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:39306253 C>T maps to NM_001398.2 *329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:39798860 G>C maps to NM_020862.1 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:39798860 G>C maps to NM_020862.1 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:40771138 G>A maps to NM_001626.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:40771138 G>A maps to NM_001626.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:41944234 G>A maps to ENST00000417807 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:41944234 G>A maps to ENST00000417807 Q110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:42753674 C>A maps to NM_006494.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:42753674 C>A maps to NM_006494.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:43411293 G>A maps to NM_002782.3 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:43411293 G>A maps to NM_002782.3 F340F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:45389235 G>A maps to NM_001042724.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:45389235 G>A maps to NM_001042724.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:46215970 G>A maps to NM_001080469.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:46215970 G>A maps to NM_001080469.1 I261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:48800517 G>T maps to NM_144577.3 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:48800517 G>T maps to NM_144577.3 I576I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:49131292 C>T maps to NM_020126.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:49131292 C>T maps to NM_020126.3 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:49519366 C>T maps to NM_000894.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:49519366 C>T maps to NM_000894.2 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50059840 C>G maps to NM_015953.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50059840 C>G maps to NM_015953.3 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50154542 G>A maps to NM_021228.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50154542 G>A maps to NM_021228.2 E299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50482461 G>A maps to NM_016440.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50482461 G>A maps to NM_016440.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50906814 C>T maps to ENST00000391817 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50906814 C>T maps to ENST00000391817 F401F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50962465 C>T maps to NM_004533.3 F898F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:50962465 C>T maps to NM_004533.3 F898F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:58438813 G>A maps to NM_133460.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:58438813 G>A maps to NM_133460.1 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:58565154 G>A maps to NM_182572.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:58565154 G>A maps to NM_182572.3 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:58906056 G>A maps to NM_001009.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:58906056 G>A maps to NM_001009.3 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:1653334 C>T maps to NM_012293.1 Q739Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:1653334 C>T maps to NM_012293.1 Q739Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:9645419 G>A maps to NM_003183.4 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:9645419 G>A maps to NM_003183.4 R473R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:11964763 G>A maps to ENST00000396099 V882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:11964763 G>A maps to ENST00000396099 V882V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:29063287 C>G maps to NM_182756.3 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:29063287 C>G maps to NM_182756.3 S268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:47705645 C>T maps to NM_000251.1 Q816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:47705645 C>T maps to NM_000251.1 Q816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:48026984 G>C maps to NM_000179.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:48026984 G>C maps to NM_000179.2 L621L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:63220777 C>T maps to NM_015252.3 F1020F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:63220777 C>T maps to NM_015252.3 F1020F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:73315527 C>G maps to NM_015470.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:73315527 C>G maps to NM_015470.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:73479987 G>A maps to NM_006429.3 *544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:73479987 G>A maps to NM_006429.3 *544*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:131487173 C>T maps to NM_207364.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:131487173 C>T maps to NM_207364.2 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:165578670 G>A maps to ENST00000392717 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:165578670 G>A maps to ENST00000392717 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:170063719 C>T maps to NM_004525.2 L2170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:170063719 C>T maps to NM_004525.2 L2170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:170396617 G>A maps to NM_024622.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:170396617 G>A maps to NM_024622.3 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:179343349 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:179343349 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:179449408 C>T maps to NM_133378.4 A19085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:179449408 C>T maps to NM_133378.4 A19085A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:191769882 G>A maps to NM_014905.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:191769882 G>A maps to NM_014905.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:200820175 G>A maps to NM_001039693.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:200820175 G>A maps to NM_001039693.2 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:200820964 G>A maps to NM_024520.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:200820964 G>A maps to NM_024520.2 A148A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:203147125 G>A maps to NM_015934.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:203147125 G>A maps to NM_015934.3 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:209007481 C>T maps to NM_005210.3 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:209007481 C>T maps to NM_005210.3 E136E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:210594967 G>A maps to NM_002374.3 E1777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:210594967 G>A maps to NM_002374.3 E1777E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:216964766 G>A maps to NM_138390.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:216964766 G>A maps to NM_138390.3 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:218686476 G>A maps to NM_022648.4 I1082I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:218686476 G>A maps to NM_022648.4 I1082I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:219103489 C>G maps to NM_005731.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:219103489 C>G maps to NM_005731.2 V124V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:219142176 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:219142176 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:222294715 G>A maps to NM_004438.3 N884N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:222294715 G>A maps to NM_004438.3 N884N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:228121063 C>G maps to NM_000091.4 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:228121063 C>G maps to NM_000091.4 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:230910659 G>T maps to NM_152527.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:230910659 G>T maps to NM_152527.4 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:234622241 C>G maps to NM_019078.1 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:234622241 C>G maps to NM_019078.1 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:238419643 C>T maps to NM_024101.5 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:238419643 C>T maps to NM_024101.5 I115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:241398600 C>T maps to NM_002081.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:241398600 C>T maps to NM_002081.2 F107F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:1902276 C>T maps to ENST00000400068 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:1902276 C>T maps to ENST00000400068 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:2597897 C>G maps to NM_080751.2 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:2597897 C>G maps to NM_080751.2 L707L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:9389807 C>A maps to NM_001172646.1 S660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:9389807 C>A maps to NM_001172646.1 S660*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:10639290 G>A maps to NM_000214.2 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:10639290 G>A maps to NM_000214.2 N173N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DR-A0ZM-01A-12D-A10S-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DR-A0ZM-01A-12D-A10S-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:34287610 C>T maps to NM_080748.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:34287610 C>T maps to NM_080748.2 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:39794457 C>G maps to NM_002660.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:39794457 C>G maps to NM_002660.2 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:43438834 G>A maps to NM_182970.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:43438834 G>A maps to NM_182970.2 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:43995670 C>T maps to NM_033542.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:43995670 C>T maps to NM_033542.3 L129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:57570796 C>T maps to NM_001336.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:57570796 C>T maps to NM_001336.3 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:57768812 C>T maps to NM_178457.1 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:57768812 C>T maps to NM_178457.1 P913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:61511607 C>G maps to NM_033081.2 L1900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:61511607 C>G maps to NM_033081.2 L1900L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:62598312 C>G maps to NM_020713.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr20:62598312 C>G maps to NM_020713.1 S103S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr21:27102095 G>A maps to NM_001003701.1 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr21:27102095 G>A maps to NM_001003701.1 Q12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr21:45736149 G>A maps to NM_002626.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr21:45736149 G>A maps to NM_002626.4 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr21:47639400 G>A maps to NM_002340.5 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr21:47639400 G>A maps to NM_002340.5 F212F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:23603577 C>T maps to NM_004327.3 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:23603577 C>T maps to NM_004327.3 Q535*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:25750767 G>A maps to NM_001135772.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:25750767 G>A maps to NM_001135772.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:29921834 G>A maps to NM_003678.4 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:29921834 G>A maps to NM_003678.4 I389I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:30722720 G>A maps to ENST00000403477 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:30722720 G>A maps to ENST00000403477 F50F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:32009452 C>T maps to NM_001007467.1 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:32009452 C>T maps to NM_001007467.1 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:36684428 C>A maps to NM_002473.4 E1601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:36684428 C>A maps to NM_002473.4 E1601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:36889850 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:36889850 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:37395883 G>A maps to NM_001163857.1 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:37395883 G>A maps to NM_001163857.1 R211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:38119858 C>T maps to NM_001039141.2 C432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:38119858 C>T maps to NM_001039141.2 C432C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:38469790 G>C maps to NM_012407.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:38469790 G>C maps to NM_012407.3 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:41832380 G>A maps to NM_016272.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:41832380 G>A maps to NM_016272.3 L323L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:42606166 C>G maps to NM_005650.1 R1715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:42606166 C>G maps to NM_005650.1 R1715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:44319877 G>A maps to NM_025225.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:44319877 G>A maps to NM_025225.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:46656321 G>C maps to NM_006071.1 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:46656321 G>C maps to NM_006071.1 L966L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:50943259 C>A maps to NM_033200.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr22:50943259 C>A maps to NM_033200.2 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:5025280 C>T maps to NM_003670.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:5025280 C>T maps to NM_003670.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:14220116 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:14220116 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:24009397 C>G maps to NM_005126.4 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:24009397 C>G maps to NM_005126.4 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:36873738 G>A maps to NM_014831.2 L2401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:36873738 G>A maps to NM_014831.2 L2401L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:38043240 G>T maps to NM_015873.3 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:38043240 G>T maps to NM_015873.3 E457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:38926867 G>C maps to ENST00000302328 S992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:38926867 G>C maps to ENST00000302328 S992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:40528734 C>G maps to NM_001145082.2 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:40528734 C>G maps to NM_001145082.2 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:48667572 G>A maps to NM_022911.2 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:48667572 G>A maps to NM_022911.2 I448I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:48699500 C>T maps to NM_001407.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:48699500 C>T maps to NM_001407.2 R189R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:49049137 G>A maps to NM_018031.3 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:49049137 G>A maps to NM_018031.3 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:49946584 C>T maps to NM_032355.3 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:49946584 C>T maps to NM_032355.3 V607V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:50252125 C>T maps to NM_006841.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:50252125 C>T maps to NM_006841.4 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:50327470 G>A maps to ENST00000336089 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:50327470 G>A maps to ENST00000336089 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:52417974 G>A maps to ENST00000273600 L2750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:52417974 G>A maps to ENST00000273600 L2750L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:52432097 C>T maps to ENST00000273600 I4067I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:52432097 C>T maps to ENST00000273600 I4067I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:56763298 C>G maps to NM_001128615.1 *559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:56763298 C>G maps to NM_001128615.1 *559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:100992562 C>G maps to NM_016247.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:100992562 C>G maps to NM_016247.2 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:101447777 G>A maps to ENST00000327230 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:101447777 G>A maps to ENST00000327230 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:108216992 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:108216992 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:112190104 G>A maps to NM_181780.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:112190104 G>A maps to NM_181780.3 L167L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:122432390 C>G maps to NM_017554.2 S1247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:122432390 C>G maps to NM_017554.2 S1247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:126137951 G>A maps to ENST00000505024 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:126137951 G>A maps to ENST00000505024 K229K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:126178540 G>A maps to NM_025112.4 Q723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:126178540 G>A maps to NM_025112.4 Q723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:127439933 G>A maps to NM_007283.5 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:127439933 G>A maps to NM_007283.5 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:150293453 C>T maps to NM_032025.3 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:150293453 C>T maps to NM_032025.3 Q468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:151067971 G>A maps to NM_053002.4 K757K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:151067971 G>A maps to NM_053002.4 K757K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:156395965 G>A maps to NM_015508.4 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:156395965 G>A maps to NM_015508.4 Q160Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:156870833 A>G maps to NM_020307.2 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:156870833 A>G maps to NM_020307.2 H200H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:156877262 C>G maps to NM_020307.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:156877262 C>G maps to NM_020307.2 A103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:169587428 G>C maps to NM_024727.2 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:169587428 G>C maps to NM_024727.2 S56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:170109007 C>G maps to NM_005414.3 S619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:170109007 C>G maps to NM_005414.3 S619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:183669664 G>A maps to NM_005688.2 R932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:183669664 G>A maps to NM_005688.2 R932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:183818402 C>G maps to NM_182589.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:183818402 C>G maps to NM_182589.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:184566916 C>A maps to ENST00000437079 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:184566916 C>A maps to ENST00000437079 G200G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:190120148 C>G maps to NM_006580.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr3:190120148 C>G maps to NM_006580.3 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:647894 G>C maps to NM_000283.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:647894 G>C maps to NM_000283.3 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:2935542 G>C maps to NM_001146069.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:2935542 G>C maps to NM_001146069.1 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:5458577 C>T maps to NM_018401.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:5458577 C>T maps to NM_018401.1 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:5862759 C>G maps to NM_001014809.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:5862759 C>G maps to NM_001014809.1 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:6622954 C>A maps to NM_015274.1 I991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:6622954 C>A maps to NM_015274.1 I991I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:13606552 C>T maps to NM_148894.2 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:13606552 C>T maps to NM_148894.2 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:39217799 C>T maps to NM_025132.3 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:39217799 C>T maps to NM_025132.3 R407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:52899626 G>A maps to NM_000232.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:52899626 G>A maps to NM_000232.4 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:56230310 C>T maps to NM_024592.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:56230310 C>T maps to NM_024592.3 F145F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:77677799 G>A maps to NM_020859.3 Q1636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:77677799 G>A maps to NM_020859.3 Q1636Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:84368044 C>T maps to NM_133636.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:84368044 C>T maps to NM_133636.2 V445V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:86916228 G>A maps to NM_001025616.2 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:86916228 G>A maps to NM_001025616.2 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:87685873 C>T maps to NM_080685.2 V1382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:87685873 C>T maps to NM_080685.2 V1382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:89941645 G>C maps to NM_014883.2 S131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:89941645 G>C maps to NM_014883.2 S131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:95223383 G>A maps to NM_014485.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:95223383 G>A maps to NM_014485.2 F116F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:96070068 C>G maps to ENST00000440890 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:96070068 C>G maps to ENST00000440890 S446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:100542385 C>T maps to ENST00000511045 F864F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:100542385 C>T maps to ENST00000511045 F864F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:103610744 C>A maps to NM_005908.3 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:103610744 C>A maps to NM_005908.3 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:113482021 C>T maps to NM_018392.4 L1609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:113482021 C>T maps to NM_018392.4 L1609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:128811390 G>C maps to NM_014264.4 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:128811390 G>C maps to NM_014264.4 V610V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:128842678 C>T maps to NM_152778.2 Q450Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:128842678 C>T maps to NM_152778.2 Q450Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:155157331 G>C maps to NM_017639.3 L2369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:155157331 G>C maps to NM_017639.3 L2369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:169842791 G>C maps to NM_001166108.1 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:169842791 G>C maps to NM_001166108.1 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:170991779 G>A maps to ENST00000509167 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:170991779 G>A maps to ENST00000509167 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:173873353 G>A maps to NM_001034845.2 W439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:173873353 G>A maps to NM_001034845.2 W439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:183664377 C>T maps to NM_001080477.1 V1145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:183664377 C>T maps to NM_001080477.1 V1145V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:188923975 G>A maps to NM_174900.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:188923975 G>A maps to NM_174900.3 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:446436 G>A maps to ENST00000315013 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:446436 G>A maps to ENST00000315013 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:5457443 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:5457443 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:7802389 C>T maps to NM_020546.2 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:7802389 C>T maps to NM_020546.2 F896F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:32091058 C>G maps to NM_178140.2 S2502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:32091058 C>G maps to NM_178140.2 S2502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:34043318 G>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:34043318 G>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:54570468 G>C maps to NM_019030.2 S888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:54570468 G>C maps to NM_019030.2 S888*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:63256874 G>A maps to NM_000524.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:63256874 G>A maps to NM_000524.2 F224F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:71494087 C>T maps to NM_005909.3 Q1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:71494087 C>T maps to NM_005909.3 Q1636*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:75581691 C>T maps to NM_014979.1 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:75581691 C>T maps to NM_014979.1 F378F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:75866442 C>G maps to NM_006633.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:75866442 C>G maps to NM_006633.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:79027908 C>G maps to NM_153610.3 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:79027908 C>G maps to NM_153610.3 L1107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:131976425 C>T maps to NM_005732.3 I1227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:131976425 C>T maps to NM_005732.3 I1227I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:132197394 C>T maps to NM_005260.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:132197394 C>T maps to NM_005260.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:134086561 C>T maps to NM_001745.2 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:134086561 C>T maps to NM_001745.2 F271F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:134364557 G>T maps to NM_002653.4 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:134364557 G>T maps to NM_002653.4 R286R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:134364762 G>C maps to NM_002653.4 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:134364762 G>C maps to NM_002653.4 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:137754896 C>T maps to NM_016604.3 Q1231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:137754896 C>T maps to NM_016604.3 Q1231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:138145809 C>T maps to ENST00000355078 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:138145809 C>T maps to ENST00000355078 R129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:140208779 C>T maps to NM_018909.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:140208779 C>T maps to NM_018909.2 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:140558367 G>A maps to NM_019120.2 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:140558367 G>A maps to NM_019120.2 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:140723924 C>T maps to NM_018916.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:140723924 C>T maps to NM_018916.3 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:150632827 C>T maps to NM_000405.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:150632827 C>T maps to NM_000405.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:150897243 C>T maps to NM_001447.2 L3800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:150897243 C>T maps to NM_001447.2 L3800L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:150897267 C>T maps to NM_001447.2 R3792R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:150897267 C>T maps to NM_001447.2 R3792R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:150932739 G>C maps to NM_001447.2 S1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:150932739 G>C maps to NM_001447.2 S1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:162902672 G>A maps to NM_001142556.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:162902672 G>A maps to NM_001142556.1 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:169689717 G>A maps to NM_005565.3 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:169689717 G>A maps to NM_005565.3 Q283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:174870217 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:174870217 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:7582904 C>T maps to NM_004415.2 Q1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:7582904 C>T maps to NM_004415.2 Q1804*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:15652367 C>A maps to NM_032122.4 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:15652367 C>A maps to NM_032122.4 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:17804678 G>T maps to NM_022113.4 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:17804678 G>T maps to NM_022113.4 L789L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:25826703 G>A maps to NM_005074.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:25826703 G>A maps to NM_005074.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:26444365 G>A maps to NM_006994.4 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:26444365 G>A maps to NM_006994.4 Q89Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:29910586 G>T maps to ENST00000376806 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:29910586 G>T maps to ENST00000376806 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:30114944 C>T maps to ENST00000376724 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:30114944 C>T maps to ENST00000376724 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:30670606 G>A maps to NM_014641.2 T1971T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:30670606 G>A maps to NM_014641.2 T1971T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:31926157 G>C maps to ENST00000375425 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:31926157 G>C maps to ENST00000375425 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:31926166 G>A maps to ENST00000375425 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:31926166 G>A maps to ENST00000375425 F26F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:33264020 C>T maps to NM_004761.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:33264020 C>T maps to NM_004761.3 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:33402937 G>A maps to NM_006772.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:33402937 G>A maps to NM_006772.2 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:35260388 G>A maps to NM_003427.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:35260388 G>A maps to NM_003427.3 S330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:36168469 C>G maps to NM_015695.2 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:36168469 C>G maps to NM_015695.2 S124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:40400384 G>C maps to NM_020737.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:40400384 G>C maps to NM_020737.1 L156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:42819891 G>C maps to NM_015349.1 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:42819891 G>C maps to NM_015349.1 L634L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:42974370 C>T maps to NM_006245.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:42974370 C>T maps to NM_006245.2 F92F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:52761708 G>A maps to NM_000847.4 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:52761708 G>A maps to NM_000847.4 I188I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:64395257 C>G maps to NM_015153.2 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:64395257 C>G maps to NM_015153.2 V545V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:89895169 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:89895169 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:96971060 G>A maps to NM_015323.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:96971060 G>A maps to NM_015323.4 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:99848495 G>A maps to NM_032870.2 R780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:99848495 G>A maps to NM_032870.2 R780*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:106960254 G>T maps to NM_001624.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:106960254 G>T maps to NM_001624.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:112439101 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:112439101 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:119245095 G>A maps to ENST00000316316 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:119245095 G>A maps to ENST00000316316 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:121768310 G>A maps to NM_000165.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:121768310 G>A maps to NM_000165.3 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:130374064 C>A maps to NM_032438.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:130374064 C>A maps to NM_032438.2 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:132910459 G>A maps to NM_003967.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:132910459 G>A maps to NM_003967.2 I122I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:134210780 C>T maps to NM_003206.3 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:134210780 C>T maps to NM_003206.3 N82N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:139564196 G>A maps to ENST00000358430 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:139564196 G>A maps to ENST00000358430 F507F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:150210679 G>C maps to NM_139165.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:150210679 G>C maps to NM_139165.1 T142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:152332809 C>G maps to NM_001122741.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:152332809 C>G maps to NM_001122741.1 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:152740726 G>A maps to NM_182961.2 Q1800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:152740726 G>A maps to NM_182961.2 Q1800*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:166918097 G>C maps to ENST00000510118 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr6:166918097 G>C maps to ENST00000510118 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:5262288 G>A maps to NM_015610.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:5262288 G>A maps to NM_015610.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:5331357 C>A maps to NM_153247.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:5331357 C>A maps to NM_153247.2 I150I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:6441587 C>T maps to NM_018890.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:6441587 C>T maps to NM_018890.3 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:21826258 G>A maps to NM_003777.3 L3212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:21826258 G>A maps to NM_003777.3 L3212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:33946487 C>T maps to NM_133468.3 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:33946487 C>T maps to NM_133468.3 D64D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:35284623 G>C maps to NM_001077653.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:35284623 G>C maps to NM_001077653.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:47880141 G>A maps to NM_138295.3 D1823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:47880141 G>A maps to NM_138295.3 D1823D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:64168505 C>T maps to NM_016220.3 H608H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:64168505 C>T maps to NM_016220.3 H608H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:74016759 G>C maps to NM_016328.2 *960Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:74016759 G>C maps to NM_016328.2 *960Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:75053459 G>C maps to ENST00000257665 S549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:75053459 G>C maps to ENST00000257665 S549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:82545960 G>A maps to NM_033026.5 R3781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:82545960 G>A maps to NM_033026.5 R3781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:90419920 C>T maps to NM_012395.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:90419920 C>T maps to NM_012395.2 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:100189464 C>T maps to NM_012172.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:100189464 C>T maps to NM_012172.4 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:103008359 C>T maps to NM_002803.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:103008359 C>T maps to NM_002803.2 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:107434304 C>T maps to NM_000111.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:107434304 C>T maps to NM_000111.2 K51K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:117232504 C>T maps to NM_000492.3 Q762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:117232504 C>T maps to NM_000492.3 Q762*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:121659176 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:121659176 G>C did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:128414593 G>A maps to NM_001708.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:128414593 G>A maps to NM_001708.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:137082126 C>A maps to NM_004717.2 E993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:137082126 C>A maps to NM_004717.2 E993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:140378977 G>A maps to NM_052853.3 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:140378977 G>A maps to NM_052853.3 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:143747857 C>A maps to NM_012365.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:143747857 C>A maps to NM_012365.1 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:147869394 G>C maps to NM_014141.5 V945V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:147869394 G>C maps to NM_014141.5 V945V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:148769446 C>T maps to NM_152411.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:148769446 C>T maps to NM_152411.3 G139G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:151859592 G>C maps to ENST00000355193 S3690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:151859592 G>C maps to ENST00000355193 S3690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:151860029 G>A maps to ENST00000355193 F3544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:151860029 G>A maps to ENST00000355193 F3544F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:158723167 C>G maps to NM_018051.4 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:158723167 C>G maps to NM_018051.4 V836V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:3046513 G>A maps to NM_033225.5 F1806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:3046513 G>A maps to NM_033225.5 F1806F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:8176254 G>A maps to NM_001080826.1 I1210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:8176254 G>A maps to NM_001080826.1 I1210I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:12957628 C>T maps to NM_182643.2 Q739Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:12957628 C>T maps to NM_182643.2 Q739Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:36766905 G>C maps to NM_001031836.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:36766905 G>C maps to NM_001031836.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:48309014 C>G maps to NM_001080394.1 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:48309014 C>G maps to NM_001080394.1 S202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:48776017 G>A maps to NM_006904.6 Q1897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:48776017 G>A maps to NM_006904.6 Q1897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:53569887 G>C maps to NM_014781.4 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:53569887 G>C maps to NM_014781.4 S834*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:57079818 C>T maps to NM_002655.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:57079818 C>T maps to NM_002655.2 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:88365922 G>A maps to NM_173538.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:88365922 G>A maps to NM_173538.2 E404E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:89068394 C>T maps to NM_005941.4 W445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:89068394 C>T maps to NM_005941.4 W445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:99208192 G>A maps to NM_024759.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:99208192 G>A maps to NM_024759.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:99264811 G>A maps to NM_024759.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:99264811 G>A maps to NM_024759.1 F85F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:131964193 G>A maps to NM_001115.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:131964193 G>A maps to NM_001115.2 I387I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:144945859 G>C maps to NM_031308.1 S521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:144945859 G>C maps to NM_031308.1 S521*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:214586 C>G maps to NM_152569.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:214586 C>G maps to NM_152569.2 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:2837401 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:2837401 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:5770129 G>A maps to ENST00000414202 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:5770129 G>A maps to ENST00000414202 L1156L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:20414064 G>C maps to NM_004529.2 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:20414064 G>C maps to NM_004529.2 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:88203304 G>C maps to ENST00000395847 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:88203304 G>C maps to ENST00000395847 L937L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:95484982 C>T maps to NM_001003800.1 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:95484982 C>T maps to NM_001003800.1 E187E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:95610230 C>A maps to NM_031486.1 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:95610230 C>A maps to NM_031486.1 E280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:97873837 C>A maps to NM_000136.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:97873837 C>A maps to NM_000136.2 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:108061568 C>T maps to NM_080546.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:108061568 C>T maps to NM_080546.3 F35F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:111668765 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:111668765 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:113261351 C>T maps to ENST00000374463 W550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:113261351 C>T maps to ENST00000374463 W550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:114454173 C>T maps to NM_173521.3 K1297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:114454173 C>T maps to NM_173521.3 K1297K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:130605494 G>A maps to NM_001114753.1 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:130605494 G>A maps to NM_001114753.1 Q33*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:131262371 G>T maps to NM_153435.1 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:131262371 G>T maps to NM_153435.1 L840L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:133769048 C>A maps to NM_198180.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:133769048 C>A maps to NM_198180.1 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:135546242 C>T maps to NM_012204.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:135546242 C>T maps to NM_012204.2 I86I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:136340662 G>C maps to NM_017585.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:136340662 G>C maps to NM_017585.3 L211L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:138454713 G>A maps to NM_002571.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:138454713 G>A maps to NM_002571.2 E95E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:139397772 G>A maps to NM_017617.3 V1676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:139397772 G>A maps to NM_017617.3 V1676V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:139418379 G>A maps to NM_017617.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:139418379 G>A maps to NM_017617.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:140349725 C>T maps to NM_001130969.1 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr9:140349725 C>T maps to NM_001130969.1 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:5821161 G>A maps to ENST00000381093 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:5821161 G>A maps to ENST00000381093 L539L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:11790740 G>T maps to NM_078629.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:11790740 G>T maps to NM_078629.3 V461V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:15266971 G>C maps to NM_001031739.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:15266971 G>C maps to NM_001031739.2 L218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:18942508 G>A maps to NM_000292.2 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:18942508 G>A maps to NM_000292.2 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:19389541 G>C maps to NM_001001671.3 S1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:19389541 G>C maps to NM_001001671.3 S1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:20071090 G>C maps to NM_001168465.1 S167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:20071090 G>C maps to NM_001168465.1 S167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:22051180 C>T maps to NM_000444.4 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:22051180 C>T maps to NM_000444.4 R20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:24225850 G>A maps to NM_003410.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:24225850 G>A maps to NM_003410.3 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:24329245 C>T maps to NM_001136233.1 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:24329245 C>T maps to NM_001136233.1 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:47034433 C>T maps to NM_005676.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:47034433 C>T maps to NM_005676.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:47435780 C>T maps to NM_006950.3 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:47435780 C>T maps to NM_006950.3 W335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:53407549 G>C maps to NM_006306.2 V1203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:53407549 G>C maps to NM_006306.2 V1203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:69652905 G>A maps to NM_001171192.1 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:69652905 G>A maps to NM_001171192.1 L581L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:71350637 G>C maps to NM_001024455.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:71350637 G>C maps to NM_001024455.3 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:76829716 C>T maps to NM_000489.3 V2108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:76829716 C>T maps to NM_000489.3 V2108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:77913089 C>T maps to NM_152694.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:77913089 C>T maps to NM_152694.2 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:85403920 C>G maps to NM_053281.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:85403920 C>G maps to NM_053281.3 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:101909940 C>G maps to NM_001184727.1 S367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:101909940 C>G maps to NM_001184727.1 S367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:104463711 C>T maps to NM_031274.3 *389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:104463711 C>T maps to NM_031274.3 *389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:110497607 C>T maps to NM_014289.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:110497607 C>T maps to NM_014289.3 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:118143098 C>G maps to NM_001031855.1 S514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:118143098 C>G maps to NM_001031855.1 S514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:118676554 C>T maps to NM_022101.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:118676554 C>T maps to NM_022101.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:135047195 G>C maps to ENST00000433339 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:135047195 G>C maps to ENST00000433339 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:150869354 C>G maps to NM_024082.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:150869354 C>G maps to NM_024082.3 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:152031144 C>G maps to NM_015922.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:152031144 C>G maps to NM_015922.2 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:153296612 G>A maps to NM_001110792.1 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chrX:153296612 G>A maps to NM_001110792.1 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:36643630 G>T maps to NM_018067.3 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:36643630 G>T maps to NM_018067.3 E513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:39341323 G>A maps to NM_030772.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:39341323 G>A maps to NM_030772.4 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:183874075 G>A maps to NM_015149.3 Q516Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:183874075 G>A maps to NM_015149.3 Q516Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:186292909 G>A maps to NM_003292.2 R2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr1:186292909 G>A maps to NM_003292.2 R2069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:14976734 G>A maps to NM_001033855.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:14976734 G>A maps to NM_001033855.1 F168F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:29581603 C>G maps to NM_032517.4 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:29581603 C>G maps to NM_032517.4 S145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:51749116 G>A maps to NM_001077665.2 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:51749116 G>A maps to NM_001077665.2 Q91Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:69726538 C>T maps to NM_022079.2 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:69726538 C>T maps to NM_022079.2 Q609Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:112839007 G>A maps to NM_000681.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:112839007 G>A maps to NM_000681.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:124672398 G>T maps to NM_001029888.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr10:124672398 G>T maps to NM_001029888.1 E83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr11:56409126 G>A maps to NM_001002925.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr11:56409126 G>A maps to NM_001002925.1 F263F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr11:65487784 C>G maps to NM_032193.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr11:65487784 C>G maps to NM_032193.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr11:124310459 G>A maps to NM_012378.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr11:124310459 G>A maps to NM_012378.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr12:51584290 C>T maps to NM_002702.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr12:51584290 C>T maps to NM_002702.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr12:104126944 G>C maps to NM_017564.9 V1815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr12:104126944 G>C maps to NM_017564.9 V1815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr12:123087421 G>A maps to NM_014708.4 S1624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr12:123087421 G>A maps to NM_014708.4 S1624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr13:32776659 C>T maps to NM_023037.2 F1338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr13:32776659 C>T maps to NM_023037.2 F1338F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr13:67801612 T>C maps to NM_203487.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr13:67801612 T>C maps to NM_203487.2 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr14:23869467 C>T maps to NM_002471.3 E526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr14:23869467 C>T maps to NM_002471.3 E526E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr15:79277489 C>T maps to NM_002891.4 V1107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr15:79277489 C>T maps to NM_002891.4 V1107V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr15:100269462 C>T maps to NM_152449.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr15:100269462 C>T maps to NM_152449.2 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr16:56531747 G>T maps to NM_031885.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr16:56531747 G>T maps to NM_031885.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr16:66995224 G>A maps to NM_024922.5 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr16:66995224 G>A maps to NM_024922.5 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:3181790 G>A maps to NM_002551.3 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:3181790 G>A maps to NM_002551.3 Q147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:7734541 C>T maps to NM_020877.2 I4123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:7734541 C>T maps to NM_020877.2 I4123I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:10248900 G>A maps to NM_003802.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:10248900 G>A maps to NM_003802.2 A432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:15976883 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:15976883 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:17248181 C>T maps to ENST00000379552 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:17248181 C>T maps to ENST00000379552 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:29553643 C>T maps to NM_001042492.2 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:29553643 C>T maps to NM_001042492.2 L731L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:60642436 C>T maps to ENST00000326270 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr17:60642436 C>T maps to ENST00000326270 R303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr18:2775769 G>A maps to NM_015295.2 A1738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr18:2775769 G>A maps to NM_015295.2 A1738A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:6732333 G>A maps to NM_001080452.1 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:6732333 G>A maps to NM_001080452.1 F355F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:14554354 G>A maps to NM_213560.1 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:14554354 G>A maps to NM_213560.1 E138E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:17678288 C>T maps to NM_024656.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:17678288 C>T maps to NM_024656.2 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:18557289 C>T maps to NM_006532.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:18557289 C>T maps to NM_006532.3 L511L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:35085426 C>T maps to NM_001025591.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:35085426 C>T maps to NM_001025591.2 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:49259544 C>T maps to NM_019113.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr19:49259544 C>T maps to NM_019113.2 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:10262999 C>T maps to NM_001165931.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:10262999 C>T maps to NM_001165931.1 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:51255078 G>A maps to ENST00000404971 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:51255078 G>A maps to ENST00000404971 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:86258467 C>T maps to NM_015425.3 E1521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:86258467 C>T maps to NM_015425.3 E1521E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:152359889 G>C maps to NM_001164507.1 V7936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:152359889 G>C maps to NM_001164507.1 V7936V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:223789233 C>T maps to NM_203372.1 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr2:223789233 C>T maps to NM_203372.1 Q405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr20:40084592 C>T maps to NM_032221.3 V952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr20:40084592 C>T maps to NM_032221.3 V952V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr20:56188279 G>A maps to NM_030776.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr20:56188279 G>A maps to NM_030776.2 S203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr21:22746205 C>T maps to NM_004540.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr21:22746205 C>T maps to NM_004540.2 V356V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr21:43786544 G>A maps to NM_003225.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr21:43786544 G>A maps to NM_003225.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr3:129236333 C>T maps to NM_052985.2 F1147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr3:129236333 C>T maps to NM_052985.2 F1147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr3:136574393 C>T maps to NM_025246.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr3:136574393 C>T maps to NM_025246.2 L364L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr4:17805706 C>A maps to NM_017741.3 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr4:17805706 C>A maps to NM_017741.3 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr4:89390327 G>A maps to NM_016323.2 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr4:89390327 G>A maps to NM_016323.2 K385K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr4:119951967 A>C maps to NM_133477.2 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr4:119951967 A>C maps to NM_133477.2 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr5:1466876 C>T maps to NM_024830.3 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr5:1466876 C>T maps to NM_024830.3 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr5:98212253 G>A maps to NM_001270.2 F1082F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr5:98212253 G>A maps to NM_001270.2 F1082F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr5:134002534 G>A maps to NM_021982.1 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr5:134002534 G>A maps to NM_021982.1 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr5:140755392 C>T maps to NM_018919.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr5:140755392 C>T maps to NM_018919.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr6:2623873 G>C maps to NM_152554.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr6:2623873 G>C maps to NM_152554.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr6:96988512 C>T maps to NM_015323.4 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr6:96988512 C>T maps to NM_015323.4 R421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:7472139 C>T maps to NM_001037763.2 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:7472139 C>T maps to NM_001037763.2 P654P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:21603846 G>A maps to NM_003777.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:21603846 G>A maps to NM_003777.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:21827104 G>A maps to NM_003777.3 L3283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:21827104 G>A maps to NM_003777.3 L3283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:44151871 C>G maps to NM_001129.3 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:44151871 C>G maps to NM_001129.3 P723P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:136700955 G>A maps to NM_001006628.1 K448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr7:136700955 G>A maps to NM_001006628.1 K448K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr8:66539549 C>T maps to NM_018120.4 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr8:66539549 C>T maps to NM_018120.4 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr9:5923061 C>T maps to NM_001017969.2 K978K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr9:5923061 C>T maps to NM_001017969.2 K978K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr9:124522190 C>T maps to ENST00000408936 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chr9:124522190 C>T maps to ENST00000408936 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chrX:135427979 G>A maps to NM_153834.3 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VK-01A-21D-A10S-08 chrX:135427979 G>A maps to NM_153834.3 L705L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:27875173 C>T maps to NM_001029882.2 Q1151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:27875173 C>T maps to NM_001029882.2 Q1151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:33065749 G>A maps to NM_001040441.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:33065749 G>A maps to NM_001040441.1 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:44433063 C>T maps to NM_014652.3 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:44433063 C>T maps to NM_014652.3 F897F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:115142026 C>T maps to ENST00000393274 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:115142026 C>T maps to ENST00000393274 P717P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:120050038 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:120050038 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:156907207 G>A maps to NM_198236.1 Q1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:156907207 G>A maps to NM_198236.1 Q1425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:184764869 G>C maps to NM_052966.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:184764869 G>C maps to NM_052966.2 L676L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:197072158 C>T maps to NM_018136.4 Q2074Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr1:197072158 C>T maps to NM_018136.4 Q2074Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr11:1103265 G>A maps to ENST00000441003 S2672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr11:1103265 G>A maps to ENST00000441003 S2672S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr11:78412895 G>A maps to NM_001098816.2 L1588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr11:78412895 G>A maps to NM_001098816.2 L1588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr11:92088451 T>C maps to ENST00000298047 I1058I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr11:92088451 T>C maps to ENST00000298047 I1058I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr12:86373206 C>A maps to ENST00000393205 G462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr12:86373206 C>A maps to ENST00000393205 G462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr12:124270379 C>T maps to NM_207437.3 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr12:124270379 C>T maps to NM_207437.3 R379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr14:103566828 G>C maps to NM_001077594.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr14:103566828 G>C maps to NM_001077594.1 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr15:72638961 G>A maps to ENST00000457859 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr15:72638961 G>A maps to ENST00000457859 F423F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr16:9858382 C>T maps to NM_000833.3 A1006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr16:9858382 C>T maps to NM_000833.3 A1006A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr17:43351846 G>A maps to ENST00000344686 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr17:43351846 G>A maps to ENST00000344686 F467F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr19:39219694 G>A maps to NM_004924.3 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr19:39219694 G>A maps to NM_004924.3 V826V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr19:51359631 C>T maps to NM_001648.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr19:51359631 C>T maps to NM_001648.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr2:202136258 C>G maps to NM_001080125.1 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr2:202136258 C>G maps to NM_001080125.1 S168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr20:33356296 C>A maps to NM_014071.2 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr20:33356296 C>A maps to NM_014071.2 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr20:37356216 C>T maps to NM_080552.2 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr20:37356216 C>T maps to NM_080552.2 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr22:21354219 C>T maps to NM_030573.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr22:21354219 C>T maps to NM_030573.2 L293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr22:41999351 A>G maps to NM_015704.2 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr22:41999351 A>G maps to NM_015704.2 C108C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr3:160951233 G>A maps to ENST00000472947 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr3:160951233 G>A maps to ENST00000472947 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr3:184800821 C>T maps to NM_001025266.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr3:184800821 C>T maps to NM_001025266.1 V242V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr4:41016311 G>C maps to NM_004307.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr4:41016311 G>C maps to NM_004307.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr4:44691409 C>T maps to NM_021927.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr4:44691409 C>T maps to NM_021927.2 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr5:118810105 A>G maps to NM_000414.3 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr5:118810105 A>G maps to NM_000414.3 E77E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr7:99696992 C>A maps to NM_005916.3 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr7:99696992 C>A maps to NM_005916.3 E104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr7:100676738 C>G maps to NM_001040105.1 S681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr7:100676738 C>G maps to NM_001040105.1 S681*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr8:42256270 A>G maps to ENST00000417062 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr8:42256270 A>G maps to ENST00000417062 K54K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr8:124042856 G>A maps to NM_024295.4 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr8:124042856 G>A maps to NM_024295.4 R85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr9:139302310 C>T maps to NM_001039707.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chr9:139302310 C>T maps to NM_001039707.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chrX:48547407 C>A maps to NM_000377.2 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VL-01A-21D-A10S-08 chrX:48547407 C>A maps to NM_000377.2 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:9932073 G>A maps to ENST00000361853 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:9932073 G>A maps to ENST00000361853 Q91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:12835063 G>A maps to NM_001080830.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:12835063 G>A maps to NM_001080830.1 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:16535285 C>T maps to NM_153213.3 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:16535285 C>T maps to NM_153213.3 E88E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:33058777 C>T maps to NM_001040441.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:33058777 C>T maps to NM_001040441.1 F82F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:45293814 G>A maps to NM_003738.4 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:45293814 G>A maps to NM_003738.4 D586D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:66713175 G>C maps to NM_001037341.1 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:66713175 G>C maps to NM_001037341.1 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:91851245 G>A maps to NM_001017975.3 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:91851245 G>A maps to NM_001017975.3 Q214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:109794626 C>T maps to NM_001408.2 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:109794626 C>T maps to NM_001408.2 V642V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:161021239 G>A maps to NM_001025598.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:161021239 G>A maps to NM_001025598.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:161092116 G>A maps to ENST00000368005 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:161092116 G>A maps to ENST00000368005 F289F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:174973856 G>A maps to NM_014412.2 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:174973856 G>A maps to NM_014412.2 K41K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:202709924 C>T maps to ENST00000367264 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:202709924 C>T maps to ENST00000367264 L1023L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:202710712 C>T maps to ENST00000367264 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:202710712 C>T maps to ENST00000367264 E945E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:207222841 T>A maps to NM_018566.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:207222841 T>A maps to NM_018566.3 V190V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:244217624 G>A maps to NM_205768.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:244217624 G>A maps to NM_205768.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:32854532 G>A maps to NM_001026383.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:32854532 G>A maps to NM_001026383.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:45878010 G>A maps to NM_000698.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:45878010 G>A maps to NM_000698.2 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:70547682 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:70547682 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:104139677 G>A maps to NM_004193.2 E1614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:104139677 G>A maps to NM_004193.2 E1614E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:115602141 G>A maps to NM_014881.3 V875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:115602141 G>A maps to NM_014881.3 V875V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:135125333 C>A maps to NM_145806.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:135125333 C>A maps to NM_145806.2 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:135125360 C>T maps to ENST00000359035 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr10:135125360 C>T maps to ENST00000359035 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:8246192 G>A maps to ENST00000428101 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:8246192 G>A maps to ENST00000428101 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:55340451 G>A maps to NM_001004701.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:55340451 G>A maps to NM_001004701.2 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:55432917 C>T maps to NM_001004704.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:55432917 C>T maps to NM_001004704.1 L92L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:57947065 C>T maps to NM_001005212.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:57947065 C>T maps to NM_001005212.3 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:77590060 G>A maps to NM_033547.3 I942I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:77590060 G>A maps to NM_033547.3 I942I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:82880509 C>T maps to NM_015885.3 Q1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:82880509 C>T maps to NM_015885.3 Q1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:94192675 C>T maps to NM_005591.3 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:94192675 C>T maps to NM_005591.3 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:103026187 C>G maps to NM_001080463.1 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:103026187 C>G maps to NM_001080463.1 L1234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:121491798 C>G maps to NM_003105.5 L1972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr11:121491798 C>G maps to NM_003105.5 L1972L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:6948233 G>A maps to NM_014262.3 W658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:6948233 G>A maps to NM_014262.3 W658*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:7637944 A>G maps to NM_004244.4 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:7637944 A>G maps to NM_004244.4 F842F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:8242797 C>G maps to NM_015509.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:8242797 C>G maps to NM_015509.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:10601864 G>A maps to NM_213658.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:10601864 G>A maps to NM_213658.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:40728938 C>G maps to NM_198578.3 L1976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:40728938 C>G maps to NM_198578.3 L1976L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:53722968 G>C maps to NM_001173467.1 S86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:53722968 G>C maps to NM_001173467.1 S86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:53823279 G>A maps to NM_020547.2 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:53823279 G>A maps to NM_020547.2 Q337Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:56625234 G>A maps to NM_001135195.1 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:56625234 G>A maps to NM_001135195.1 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:58002421 C>T maps to NM_178502.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:58002421 C>T maps to NM_178502.2 L290L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:117993044 G>A maps to ENST00000339824 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:117993044 G>A maps to ENST00000339824 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:130827567 C>T maps to NM_004764.4 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr12:130827567 C>T maps to NM_004764.4 Q38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr14:55650366 G>A maps to NM_014750.4 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr14:55650366 G>A maps to NM_014750.4 R115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr14:81259399 G>A maps to NM_152446.3 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr14:81259399 G>A maps to NM_152446.3 R422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr14:88892579 C>G maps to NM_018418.4 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr14:88892579 C>G maps to NM_018418.4 S126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr14:94152931 G>A maps to ENST00000393153 A2339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr14:94152931 G>A maps to ENST00000393153 A2339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:40099334 G>A maps to NM_007223.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:40099334 G>A maps to NM_007223.1 I99I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:64496788 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:64496788 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:99500352 C>T maps to NM_000875.3 I1262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:99500352 C>T maps to NM_000875.3 I1262I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:99500355 C>A maps to NM_000875.3 I1263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:99500355 C>A maps to NM_000875.3 I1263I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:100695465 G>C maps to NM_139057.2 S414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr15:100695465 G>C maps to NM_139057.2 S414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:24166138 G>A maps to NM_002738.6 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:24166138 G>A maps to NM_002738.6 P400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:30081307 G>A maps to ENST00000395248 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:30081307 G>A maps to ENST00000395248 E373E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:30485562 C>T maps to NM_002209.2 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:30485562 C>T maps to NM_002209.2 F36F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:46655177 G>A maps to NM_024745.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:46655177 G>A maps to NM_024745.4 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:67432777 G>C maps to NM_013304.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:67432777 G>C maps to NM_013304.2 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:70843796 C>T maps to NM_032821.2 T4923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:70843796 C>T maps to NM_032821.2 T4923T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:72821170 G>A maps to NM_006885.3 L3668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:72821170 G>A maps to NM_006885.3 L3668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:81190477 G>A maps to NM_052892.3 Q1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr16:81190477 G>A maps to NM_052892.3 Q1371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:7099653 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:7099653 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:7357784 C>G maps to NM_000747.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:7357784 C>G maps to NM_000747.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:7804194 C>T maps to NM_001005271.2 R1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:7804194 C>T maps to NM_001005271.2 R1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:12899992 C>T maps to NM_018127.6 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:12899992 C>T maps to NM_018127.6 T510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:32904623 G>A maps to NM_207454.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:32904623 G>A maps to NM_207454.2 I142I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:72832423 C>T maps to NM_017728.3 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:72832423 C>T maps to NM_017728.3 F363F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:73559177 C>T maps to NM_001031803.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:73559177 C>T maps to NM_001031803.1 I204I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:73838974 C>T maps to ENST00000412096 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:73838974 C>T maps to ENST00000412096 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:78332127 C>T maps to NM_020914.4 L3684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:78332127 C>T maps to NM_020914.4 L3684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:78355465 C>T maps to NM_020914.4 I4688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr17:78355465 C>T maps to NM_020914.4 I4688I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr18:20573282 C>A maps to ENST00000360790 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr18:20573282 C>A maps to ENST00000360790 S498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr18:29784240 C>G maps to NM_005925.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr18:29784240 C>G maps to NM_005925.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:16495996 G>A maps to ENST00000455140 F730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:16495996 G>A maps to ENST00000455140 F730F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:33587165 C>T maps to NM_018025.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:33587165 C>T maps to NM_018025.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:36106005 C>T maps to NM_015302.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:36106005 C>T maps to NM_015302.1 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:41083467 C>T maps to NM_138392.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:41083467 C>T maps to NM_138392.3 F64F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:50661603 G>T maps to NM_152358.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:50661603 G>T maps to NM_152358.2 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:50753909 C>T maps to NM_001145809.1 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:50753909 C>T maps to NM_001145809.1 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:58806466 G>A maps to NM_021089.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr19:58806466 G>A maps to NM_021089.2 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:17941368 C>T maps to NM_001130009.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:17941368 C>T maps to NM_001130009.1 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:20871109 C>G maps to NM_182828.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:20871109 C>G maps to NM_182828.2 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:45704133 G>A maps to NM_018079.4 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:45704133 G>A maps to NM_018079.4 Q683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:50765724 C>T maps to ENST00000404971 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:50765724 C>T maps to ENST00000404971 E643E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:55459971 C>T maps to NM_001177413.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:55459971 C>T maps to NM_001177413.1 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:102851513 C>G maps to NM_003854.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:102851513 C>G maps to NM_003854.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:103095451 C>A maps to NM_001011552.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:103095451 C>A maps to NM_001011552.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:108489229 G>A maps to NM_182588.2 Q1590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:108489229 G>A maps to NM_182588.2 Q1590Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:128340009 C>T maps to ENST00000389524 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:128340009 C>T maps to ENST00000389524 F444F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:148654035 G>A maps to NM_001616.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:148654035 G>A maps to NM_001616.3 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:162903472 G>A maps to NM_001935.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:162903472 G>A maps to NM_001935.3 F79F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:179427449 G>A maps to NM_133378.4 V25235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:179427449 G>A maps to NM_133378.4 V25235V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:179579851 C>T maps to NM_133378.4 K7443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:179579851 C>T maps to NM_133378.4 K7443K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:190329968 G>A maps to NM_032168.1 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:190329968 G>A maps to NM_032168.1 K426K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:203407067 G>A maps to NM_001204.6 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr2:203407067 G>A maps to NM_001204.6 Q437Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr20:43836629 C>G maps to NM_003007.3 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr20:43836629 C>G maps to NM_003007.3 S231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:10142945 G>C maps to NM_001018115.1 *1452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:10142945 G>C maps to NM_001018115.1 *1452Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:97983233 C>T maps to NM_001005479.1 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:97983233 C>T maps to NM_001005479.1 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:100413634 G>A maps to NM_032787.2 Q728Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:100413634 G>A maps to NM_032787.2 Q728Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:112198560 G>A maps to NM_181780.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:112198560 G>A maps to NM_181780.3 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:115560716 G>A maps to NM_002338.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:115560716 G>A maps to NM_002338.3 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:196532221 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr3:196532221 G>A did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:7725533 C>T maps to NM_020777.2 P845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:7725533 C>T maps to NM_020777.2 P845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:17839397 C>T maps to NM_022346.3 Q814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:17839397 C>T maps to NM_022346.3 Q814*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:39507310 G>A maps to NM_003359.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:39507310 G>A maps to NM_003359.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:111119452 G>A maps to NM_024090.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:111119452 G>A maps to NM_024090.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:148407186 G>A maps to NM_001957.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:148407186 G>A maps to NM_001957.3 L118L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:184240978 G>A maps to NM_001111319.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:184240978 G>A maps to NM_001111319.1 V131V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:185683649 G>A maps to NM_001995.2 Q517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr4:185683649 G>A maps to NM_001995.2 Q517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:79025922 A>G maps to NM_153610.3 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:79025922 A>G maps to NM_153610.3 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:86564632 C>A maps to NM_002890.1 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:86564632 C>A maps to NM_002890.1 S122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:140263385 C>T maps to NM_018904.2 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:140263385 C>T maps to NM_018904.2 H511H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:169494638 G>C maps to NM_004946.2 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:169494638 G>C maps to NM_004946.2 L1531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:179201030 C>G maps to NM_014757.4 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:179201030 C>G maps to NM_014757.4 S735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:179201367 C>T maps to NM_014757.4 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr5:179201367 C>T maps to NM_014757.4 L847L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:32007218 C>T maps to NM_000500.5 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:32007218 C>T maps to NM_000500.5 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:55625296 C>T maps to NM_021073.2 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:55625296 C>T maps to NM_021073.2 K354K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:56506863 C>T maps to ENST00000361203 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:56506863 C>T maps to ENST00000361203 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:124979387 G>A maps to NM_001040214.1 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:124979387 G>A maps to NM_001040214.1 E110E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:168443352 G>A maps to NM_030615.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr6:168443352 G>A maps to NM_030615.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr7:65599340 G>A maps to ENST00000450043 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr7:65599340 G>A maps to ENST00000450043 L255L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr7:84642131 G>A maps to NM_152754.2 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr7:84642131 G>A maps to NM_152754.2 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr7:113558803 C>T maps to NM_002711.3 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr7:113558803 C>T maps to NM_002711.3 W83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr7:151917763 G>A maps to ENST00000355193 Q1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr7:151917763 G>A maps to ENST00000355193 Q1186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr8:100589800 C>G maps to NM_017890.3 L1745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr8:100589800 C>G maps to NM_017890.3 L1745L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr8:124408480 G>C maps to NM_014109.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr8:124408480 G>C maps to NM_014109.3 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr8:143995804 C>A maps to NM_000498.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr8:143995804 C>A maps to NM_000498.3 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr9:6251260 C>T maps to NM_033439.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr9:6251260 C>T maps to NM_033439.3 I113I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:1531690 G>A maps to NM_004192.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:1531690 G>A maps to NM_004192.3 L527L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:21675599 G>A maps to NM_153270.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:21675599 G>A maps to NM_153270.1 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:37312805 G>T maps to NM_000950.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:37312805 G>T maps to NM_000950.2 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:46532050 G>A maps to NM_032591.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:46532050 G>A maps to NM_032591.1 F205F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:47062947 G>C maps to NM_153280.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:47062947 G>C maps to NM_153280.2 A476A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:49958364 G>A maps to NM_003886.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:49958364 G>A maps to NM_003886.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:54982617 G>A maps to NM_002625.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:54982617 G>A maps to NM_002625.2 V202V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:75003458 G>A maps to NM_138703.4 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:75003458 G>A maps to NM_138703.4 I476I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:79955473 C>T maps to NM_153252.4 W975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chrX:79955473 C>T maps to NM_153252.4 W975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:11900255 G>A maps to NM_001286.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:11900255 G>A maps to NM_001286.2 L862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:31896550 C>T maps to NM_178865.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:31896550 C>T maps to NM_178865.4 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:155931935 C>T maps to NM_001162383.1 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:155931935 C>T maps to NM_001162383.1 K393K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:167852752 G>A maps to NM_018417.4 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:167852752 G>A maps to NM_018417.4 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:227152738 C>T maps to NM_020247.4 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr1:227152738 C>T maps to NM_020247.4 F72F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr10:120917550 C>T maps to NM_213649.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr10:120917550 C>T maps to NM_213649.1 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:62491177 G>A maps to NM_001079559.1 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:62491177 G>A maps to NM_001079559.1 Q258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:66366698 C>G maps to NM_005125.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:66366698 C>G maps to NM_005125.1 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:67174344 G>A maps to NM_198517.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:67174344 G>A maps to NM_198517.2 R232R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:94341822 C>T maps to NM_152431.2 C638C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr11:94341822 C>T maps to NM_152431.2 C638C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr12:131359154 G>A maps to ENST00000392369 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr12:131359154 G>A maps to ENST00000392369 W124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr13:114780742 C>G maps to ENST00000389544 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr13:114780742 C>G maps to ENST00000389544 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:21502045 G>C maps to NM_001012264.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:21502045 G>C maps to NM_001012264.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:99865318 C>T maps to NM_032233.2 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:99865318 C>T maps to NM_032233.2 E494E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:100705961 C>T maps to NM_003403.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:100705961 C>T maps to NM_003403.3 F127F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:105417014 G>A maps to NM_138420.2 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr14:105417014 G>A maps to NM_138420.2 L1591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr15:43928407 C>T maps to NM_172095.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr15:43928407 C>T maps to NM_172095.1 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr15:90903974 G>A maps to NM_001004309.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr15:90903974 G>A maps to NM_001004309.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr16:773854 A>G did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr16:773854 A>G did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr16:21994416 G>A maps to NM_003366.2 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr16:21994416 G>A maps to NM_003366.2 K429K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr16:67573990 G>A maps to NM_001193523.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr16:67573990 G>A maps to NM_001193523.1 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr16:69727753 C>G maps to NM_138713.2 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr16:69727753 C>G maps to NM_138713.2 P1342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr17:18528734 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr17:18528734 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr17:29528440 C>T maps to NM_001042492.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr17:29528440 C>T maps to NM_001042492.2 Q400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr17:53798407 C>T maps to NM_001099640.1 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr17:53798407 C>T maps to NM_001099640.1 E8E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr17:74041398 G>A maps to NM_014230.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr17:74041398 G>A maps to NM_014230.2 L456L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:2477086 C>T maps to NM_015675.3 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:2477086 C>T maps to NM_015675.3 I69I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:12903535 C>T maps to NM_002229.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:12903535 C>T maps to NM_002229.2 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:14627858 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:14627858 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:17374920 G>A maps to NM_031941.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:17374920 G>A maps to NM_031941.3 V31V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:49260186 C>G maps to NM_019113.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:49260186 C>G maps to NM_019113.2 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:50295237 C>T maps to NM_014203.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:50295237 C>T maps to NM_014203.2 R174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:55497594 C>T maps to NM_017852.3 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr19:55497594 C>T maps to NM_017852.3 L760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr2:27276284 C>T maps to NM_021831.5 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr2:27276284 C>T maps to NM_021831.5 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr2:112995976 T>C maps to NM_032494.2 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr2:112995976 T>C maps to NM_032494.2 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr20:2474594 G>C did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr20:2474594 G>C did not map to a codon.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr20:61542822 G>A maps to NM_033081.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr20:61542822 G>A maps to NM_033081.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr20:62195545 G>A maps to NM_001037335.2 S1543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr20:62195545 G>A maps to NM_001037335.2 S1543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr21:45104457 C>T maps to NM_015056.2 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr21:45104457 C>T maps to NM_015056.2 R306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr21:47929215 G>C maps to ENST00000318711 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr21:47929215 G>C maps to ENST00000318711 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr22:30866216 C>T maps to NM_174975.4 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr22:30866216 C>T maps to NM_174975.4 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr22:41652026 G>A maps to NM_002883.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr22:41652026 G>A maps to NM_002883.2 L357L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:14170985 G>A maps to NM_024334.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:14170985 G>A maps to NM_024334.2 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:14170991 G>A maps to NM_024334.2 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:14170991 G>A maps to NM_024334.2 E31E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:150127937 G>A maps to NM_014779.2 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:150127937 G>A maps to NM_014779.2 Q267Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:197616499 G>C maps to NM_001134435.1 S428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr3:197616499 G>C maps to NM_001134435.1 S428*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr4:153247244 A>T maps to NM_033632.2 Y519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr4:153247244 A>T maps to NM_033632.2 Y519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr5:154092619 G>A maps to NM_015315.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr5:154092619 G>A maps to NM_015315.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr6:27420476 G>A maps to NM_007149.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr6:27420476 G>A maps to NM_007149.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr6:139206713 G>A maps to NM_001195037.2 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr6:139206713 G>A maps to NM_001195037.2 L700L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr6:155764526 G>A maps to NM_015718.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr6:155764526 G>A maps to NM_015718.2 F122F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr7:2972190 C>T maps to NM_032415.4 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr7:2972190 C>T maps to NM_032415.4 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr9:80855102 C>T maps to NM_001098802.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr9:80855102 C>T maps to NM_001098802.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr9:115806339 C>T maps to NM_003408.1 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr9:115806339 C>T maps to NM_003408.1 Q186Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chrX:71350358 G>A maps to NM_001024455.3 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chrX:71350358 G>A maps to NM_001024455.3 Y344Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chrX:125685754 C>A maps to NM_178470.4 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chrX:125685754 C>A maps to NM_178470.4 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chrX:154490501 G>A maps to NM_171998.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chrX:154490501 G>A maps to NM_171998.2 R76R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:2938789 C>T maps to NM_080431.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:2938789 C>T maps to NM_080431.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:8390356 C>G maps to ENST00000377479 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:8390356 C>G maps to ENST00000377479 V302V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:16892231 G>C maps to NM_017940.3 S988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:16892231 G>C maps to NM_017940.3 S988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:22456274 C>G maps to NM_030761.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:22456274 C>G maps to NM_030761.4 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:29435894 T>C maps to NM_001166005.1 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:29435894 T>C maps to NM_001166005.1 A787A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:34190971 G>A maps to ENST00000373381 I851I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:34190971 G>A maps to ENST00000373381 I851I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858592 C>T maps to NM_003517.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858592 C>T maps to NM_003517.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858607 A>G maps to NM_003517.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858607 A>G maps to NM_003517.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858655 G>C maps to NM_003517.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858655 G>C maps to NM_003517.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858661 C>A maps to NM_003517.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858661 C>A maps to NM_003517.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858706 C>G maps to NM_003517.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858706 C>G maps to NM_003517.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858709 G>A maps to NM_003517.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858709 G>A maps to NM_003517.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858712 C>T maps to NM_003517.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858712 C>T maps to NM_003517.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858772 C>T maps to NM_003517.2 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858772 C>T maps to NM_003517.2 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858775 C>G maps to NM_003517.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858775 C>G maps to NM_003517.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858802 A>G maps to NM_003517.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858802 A>G maps to NM_003517.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858832 C>T maps to NM_003517.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858832 C>T maps to NM_003517.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858853 T>C maps to NM_003517.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858853 T>C maps to NM_003517.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858886 C>G maps to NM_003517.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149858886 C>G maps to NM_003517.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859277 A>G maps to NM_175065.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859277 A>G maps to NM_175065.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859280 T>C maps to NM_175065.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859280 T>C maps to NM_175065.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859283 C>G maps to NM_175065.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859283 C>G maps to NM_175065.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859328 T>G maps to NM_175065.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859328 T>G maps to NM_175065.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859334 G>C maps to NM_175065.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859334 G>C maps to NM_175065.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859382 C>T maps to NM_175065.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859382 C>T maps to NM_175065.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859397 A>G maps to NM_175065.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859397 A>G maps to NM_175065.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859427 A>G maps to NM_175065.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:149859427 A>G maps to NM_175065.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152324876 G>A maps to NM_001014342.2 T1795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152324876 G>A maps to NM_001014342.2 T1795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152327909 G>A maps to NM_001014342.2 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152327909 G>A maps to NM_001014342.2 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152328221 A>G maps to NM_001014342.2 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152328221 A>G maps to NM_001014342.2 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777598 C>T maps to NM_178351.3 *119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777598 C>T maps to NM_178351.3 *119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777627 C>G maps to NM_178351.3 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777627 C>G maps to NM_178351.3 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777630 C>T maps to NM_178351.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777630 C>T maps to NM_178351.3 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777633 G>T maps to NM_178351.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777633 G>T maps to NM_178351.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777756 T>A maps to NM_178351.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777756 T>A maps to NM_178351.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777780 G>T maps to NM_178351.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777780 G>T maps to NM_178351.3 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777843 G>A maps to NM_178351.3 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152777843 G>A maps to NM_178351.3 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152785038 A>T maps to NM_178349.1 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152785038 A>T maps to NM_178349.1 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152785119 T>A maps to NM_178349.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152785119 T>A maps to NM_178349.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152785245 A>G maps to NM_178349.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152785245 A>G maps to NM_178349.1 G108G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152785277 A>G maps to NM_178349.1 *119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:152785277 A>G maps to NM_178349.1 *119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:153907296 C>T maps to NM_014856.2 Q904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:153907296 C>T maps to NM_014856.2 Q904Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:156714016 C>A maps to NM_001126050.1 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:156714016 C>A maps to NM_001126050.1 E159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:159505611 G>A maps to NM_001004469.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:159505611 G>A maps to NM_001004469.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:186307242 G>C maps to NM_003292.2 V1428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:186307242 G>C maps to NM_003292.2 V1428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:228645895 A>G maps to NM_175055.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:228645895 A>G maps to NM_175055.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:228646075 A>G maps to NM_175055.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr1:228646075 A>G maps to NM_175055.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr10:5966419 G>T maps to NM_032807.3 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr10:5966419 G>T maps to NM_032807.3 E900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr10:93748985 C>T maps to NM_003972.2 R835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr10:93748985 C>T maps to NM_003972.2 R835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr10:100177437 G>A maps to NM_000195.2 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr10:100177437 G>A maps to NM_000195.2 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:308197 C>T maps to NM_006435.2 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:308197 C>T maps to NM_006435.2 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:314271 C>T maps to ENST00000328221 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:314271 C>T maps to ENST00000328221 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:320798 G>C maps to NM_021034.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:320798 G>C maps to NM_021034.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1606410 G>A maps to NM_001005922.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1606410 G>A maps to NM_001005922.1 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1642783 G>A maps to NM_001012709.1 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1642783 G>A maps to NM_001012709.1 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1642816 A>G maps to NM_001012709.1 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1642816 A>G maps to NM_001012709.1 G169G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1642879 A>G maps to NM_001012709.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1642879 A>G maps to NM_001012709.1 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1643071 A>G maps to ENST00000359229 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1643071 A>G maps to ENST00000359229 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1651090 C>T maps to NM_001001480.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1651090 C>T maps to NM_001001480.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1651567 C>T maps to NM_001001480.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1651567 C>T maps to NM_001001480.2 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1651759 C>T maps to NM_001001480.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:1651759 C>T maps to NM_001001480.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:3832617 C>G maps to NM_014489.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:3832617 C>G maps to NM_014489.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:10527269 C>T maps to NM_000480.2 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:10527269 C>T maps to NM_000480.2 L724L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:55541500 C>T maps to NM_001001967.1 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:55541500 C>T maps to NM_001001967.1 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:56431575 C>T maps to NM_001004730.1 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:56431575 C>T maps to NM_001004730.1 Q139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57971419 G>A maps to NM_001004459.1 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57971419 G>A maps to NM_001004459.1 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57971446 G>A maps to NM_001004459.1 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57971446 G>A maps to NM_001004459.1 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57971520 G>A maps to NM_001004459.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57971520 G>A maps to NM_001004459.1 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57971548 T>C maps to NM_001004459.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57971548 T>C maps to NM_001004459.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57971563 G>A maps to NM_001004459.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57971563 G>A maps to NM_001004459.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982320 G>A maps to NM_001004458.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982320 G>A maps to NM_001004458.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982422 T>C maps to NM_001004458.1 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982422 T>C maps to NM_001004458.1 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982449 T>C maps to NM_001004458.1 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982449 T>C maps to NM_001004458.1 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982521 T>C maps to NM_001004458.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982521 T>C maps to NM_001004458.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982596 C>T maps to NM_001004458.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982596 C>T maps to NM_001004458.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982698 A>G maps to NM_001004458.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982698 A>G maps to NM_001004458.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982902 T>C maps to NM_001004458.1 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982902 T>C maps to NM_001004458.1 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982941 T>A maps to NM_001004458.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:57982941 T>A maps to NM_001004458.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:59481177 G>A maps to NM_001005324.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:59481177 G>A maps to NM_001005324.1 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:60183672 C>G maps to NM_032597.3 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:60183672 C>G maps to NM_032597.3 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:61249900 G>A did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:61249900 G>A did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:65822728 G>A maps to NM_006842.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:65822728 G>A maps to NM_006842.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71238804 T>C maps to NM_001012503.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71238804 T>C maps to NM_001012503.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71277139 G>A maps to NM_001012710.1 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71277139 G>A maps to NM_001012710.1 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71277196 T>C maps to NM_001012710.1 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71277196 T>C maps to NM_001012710.1 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71293457 G>A maps to ENST00000376535 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71293457 G>A maps to ENST00000376535 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71293544 T>C maps to ENST00000376535 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71293544 T>C maps to ENST00000376535 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71293766 A>G maps to ENST00000376535 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71293766 A>G maps to ENST00000376535 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71293847 A>G maps to ENST00000376535 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:71293847 A>G maps to ENST00000376535 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900574 T>C maps to NM_001004464.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900574 T>C maps to NM_001004464.1 T82T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900589 T>C maps to NM_001004464.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900589 T>C maps to NM_001004464.1 S87S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900634 C>T maps to NM_001004464.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900634 C>T maps to NM_001004464.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900637 T>C maps to NM_001004464.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900637 T>C maps to NM_001004464.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900646 A>G maps to NM_001004464.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900646 A>G maps to NM_001004464.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900695 C>T maps to ENST00000375021 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900695 C>T maps to ENST00000375021 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900843 G>A maps to ENST00000375021 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900843 G>A maps to ENST00000375021 W172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900916 T>G maps to ENST00000375021 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123900916 T>G maps to ENST00000375021 T196T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123901198 G>A maps to ENST00000375021 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123901198 G>A maps to ENST00000375021 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123901210 G>A maps to ENST00000375021 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123901210 G>A maps to ENST00000375021 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123908826 T>C maps to NM_001004463.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123908826 T>C maps to NM_001004463.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123908838 T>C maps to NM_001004463.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123908838 T>C maps to NM_001004463.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123908868 A>G maps to NM_001004463.1 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123908868 A>G maps to NM_001004463.1 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123909399 G>A maps to NM_001004463.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123909399 G>A maps to NM_001004463.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123909402 A>G maps to NM_001004463.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123909402 A>G maps to NM_001004463.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123909513 G>C maps to NM_001004463.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:123909513 G>C maps to NM_001004463.1 S65S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:11506463 C>T maps to NM_005039.3 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:11506463 C>T maps to NM_005039.3 Q191Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:21971158 G>A maps to NM_005691.2 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:21971158 G>A maps to NM_005691.2 L1232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:49438016 C>T maps to NM_003482.3 A1718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:49438016 C>T maps to NM_003482.3 A1718A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52681030 G>A maps to NM_002281.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52681030 G>A maps to NM_002281.3 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52681046 A>G maps to NM_002281.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52681046 A>G maps to NM_002281.3 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52698741 A>G maps to NM_002284.3 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52698741 A>G maps to NM_002284.3 K222K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52699040 G>A maps to NM_002284.3 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52699040 G>A maps to NM_002284.3 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52699121 C>T maps to NM_002284.3 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52699121 C>T maps to NM_002284.3 I278I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52710789 T>C maps to NM_002282.3 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:52710789 T>C maps to NM_002282.3 Q256Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:55688302 G>A maps to NM_001005493.1 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:55688302 G>A maps to NM_001005493.1 T238T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:56234911 C>T maps to NM_002429.4 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:56234911 C>T maps to NM_002429.4 K94K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:70004510 C>G maps to NM_201550.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:70004510 C>G maps to NM_201550.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:124416369 G>A maps to NM_207437.3 T4250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr12:124416369 G>A maps to NM_207437.3 T4250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr13:32910967 G>T maps to NM_000059.3 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr13:32910967 G>T maps to NM_000059.3 E826*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr13:46549611 C>T maps to ENST00000242848 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr13:46549611 C>T maps to ENST00000242848 R758R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr13:96293692 C>G maps to NM_198968.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr13:96293692 C>G maps to NM_198968.2 L151L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr13:108862230 C>T maps to NM_001098268.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr13:108862230 C>T maps to NM_001098268.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr14:65494227 C>T maps to ENST00000448390 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr14:65494227 C>T maps to ENST00000448390 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr14:72936740 C>G maps to NM_004296.4 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr14:72936740 C>G maps to NM_004296.4 A162A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr14:95081320 C>T maps to ENST00000393080 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr14:95081320 C>T maps to ENST00000393080 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr15:45433187 T>C maps to NM_175940.1 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr15:45433187 T>C maps to NM_175940.1 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr15:67878264 G>T maps to NM_145160.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr15:67878264 G>T maps to NM_145160.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3063464 C>T maps to NM_020982.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3063464 C>T maps to NM_020982.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3063578 T>G maps to NM_020982.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3063578 T>G maps to NM_020982.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3063599 C>T maps to NM_020982.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3063599 C>T maps to NM_020982.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3063858 C>T maps to NM_020982.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3063858 C>T maps to NM_020982.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3065845 G>C maps to NM_021195.4 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3065845 G>C maps to NM_021195.4 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3065920 A>G maps to NM_021195.4 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3065920 A>G maps to NM_021195.4 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3065947 A>G maps to NM_021195.4 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:3065947 A>G maps to NM_021195.4 C25C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:4848113 G>T maps to NM_024589.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:4848113 G>T maps to NM_024589.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:5125492 T>A maps to NM_019109.4 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:5125492 T>A maps to NM_019109.4 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:31374541 T>C maps to NM_000887.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:31374541 T>C maps to NM_000887.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:31374553 G>A maps to NM_000887.3 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:31374553 G>A maps to NM_000887.3 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:31374577 G>C maps to NM_000887.3 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:31374577 G>C maps to NM_000887.3 V531V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:31374634 G>A maps to NM_000887.3 R550R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:31374634 G>A maps to NM_000887.3 R550R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DS-A1OC-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-DS-A1OC-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:56704828 C>T maps to NM_005951.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:56704828 C>T maps to NM_005951.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:56704894 T>C maps to NM_005951.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:56704894 T>C maps to NM_005951.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:57764925 G>C maps to NM_032269.5 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:57764925 G>C maps to NM_032269.5 L825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:57996485 A>G maps to NM_001297.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr16:57996485 A>G maps to NM_001297.4 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:18634441 G>A maps to NM_001037330.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:18634441 G>A maps to NM_001037330.1 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:26942771 C>A maps to NM_014680.2 L2145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:26942771 C>A maps to NM_014680.2 L2145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:33984791 A>G maps to NM_001030006.1 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:33984791 A>G maps to NM_001030006.1 G657G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39253967 G>A maps to NM_031960.2 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39253967 G>A maps to NM_031960.2 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39254153 C>T maps to NM_031960.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39254153 C>T maps to NM_031960.2 Q61Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39254183 T>C maps to NM_031960.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39254183 T>C maps to NM_031960.2 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39254297 T>C maps to NM_031960.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39254297 T>C maps to NM_031960.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39261684 C>T maps to NM_001146041.1 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39261684 C>T maps to NM_001146041.1 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39261699 T>C maps to NM_001146041.1 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39261699 T>C maps to NM_001146041.1 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39261861 T>C maps to NM_001146041.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39261861 T>C maps to NM_001146041.1 C74C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39261891 T>C maps to NM_001146041.1 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39261891 T>C maps to NM_001146041.1 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39261975 G>C maps to NM_001146041.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39261975 G>C maps to NM_001146041.1 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39262014 T>C maps to ENST00000377731 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39262014 T>C maps to ENST00000377731 C120C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39274273 A>G maps to NM_033059.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:39274273 A>G maps to NM_033059.3 T98T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:40266553 G>A maps to NM_021078.2 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:40266553 G>A maps to NM_021078.2 F696F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:40556935 C>T maps to NM_012232.5 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:40556935 C>T maps to NM_012232.5 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr18:34320695 C>G maps to NM_025135.2 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr18:34320695 C>G maps to NM_025135.2 P1043P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:1432666 A>C maps to NM_018959.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:1432666 A>C maps to NM_018959.2 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:4234820 G>A maps to NM_005755.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:4234820 G>A maps to NM_005755.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:5622546 G>C maps to NM_014649.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:5622546 G>C maps to NM_014649.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:6177304 T>C maps to NM_030924.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:6177304 T>C maps to NM_030924.3 V268V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:8615214 C>A maps to NM_012335.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:8615214 C>A maps to NM_012335.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:9048426 T>C maps to NM_024690.2 E11068E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:9048426 T>C maps to NM_024690.2 E11068E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:9058346 G>C maps to NM_024690.2 S9700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:9058346 G>C maps to NM_024690.2 S9700*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:9325126 T>G maps to NM_001005191.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:9325126 T>G maps to NM_001005191.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:12575151 C>T maps to ENST00000428311 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:12575151 C>T maps to ENST00000428311 G528G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:18179318 G>A maps to NM_005535.1 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:18179318 G>A maps to NM_005535.1 R403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:19905507 C>G maps to NM_001099269.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:19905507 C>G maps to NM_001099269.2 P396P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:21366047 G>A maps to NM_133473.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:21366047 G>A maps to NM_133473.2 K314K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:22156020 A>T maps to NM_007153.3 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:22156020 A>T maps to NM_007153.3 G605G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:22939434 C>T maps to ENST00000397104 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:22939434 C>T maps to ENST00000397104 G912G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:23542774 T>A maps to NM_003430.2 A1002A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:23542774 T>A maps to NM_003430.2 A1002A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:23836696 T>G maps to NM_138330.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:23836696 T>G maps to NM_138330.2 G346G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:23836723 T>C maps to NM_138330.2 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:23836723 T>C maps to NM_138330.2 E337E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:23836732 A>G maps to NM_138330.2 H334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:23836732 A>G maps to NM_138330.2 H334H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:40902680 C>T maps to NM_181882.2 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:40902680 C>T maps to NM_181882.2 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:41122876 A>T maps to ENST00000308370 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:41122876 A>T maps to ENST00000308370 T1032T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:46027911 G>A maps to NM_003370.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:46027911 G>A maps to NM_003370.3 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:51331008 G>A maps to NM_017509.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:51331008 G>A maps to NM_017509.2 Q36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:53958909 A>G maps to NM_001008401.3 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:53958909 A>G maps to NM_001008401.3 K383K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:55349097 C>T maps to NM_012314.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:55349097 C>T maps to NM_012314.3 I46I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56228095 C>G maps to NM_176820.2 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56228095 C>G maps to NM_176820.2 L776L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56701663 C>T maps to NM_001080456.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56701663 C>T maps to NM_001080456.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56701711 T>C maps to NM_001080456.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56701711 T>C maps to NM_001080456.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56733045 G>A maps to NM_024303.1 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56733045 G>A maps to NM_024303.1 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56733267 A>G maps to NM_024303.1 C389C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56733267 A>G maps to NM_024303.1 C389C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56733279 T>C maps to NM_024303.1 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56733279 T>C maps to NM_024303.1 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56733993 C>A maps to NM_024303.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:56733993 C>A maps to NM_024303.1 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:57967116 G>C maps to NM_020633.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:57967116 G>C maps to NM_020633.2 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:58370844 G>A maps to NM_032828.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr19:58370844 G>A maps to NM_032828.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:71827923 G>A maps to NM_001130987.1 Q1283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:71827923 G>A maps to NM_001130987.1 Q1283Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:111413328 A>G maps to NM_004336.3 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:111413328 A>G maps to NM_004336.3 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:179469032 C>G did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:179469032 C>G did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:191175494 G>C maps to NM_014362.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:191175494 G>C maps to NM_014362.3 T21T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:196729154 A>G maps to NM_018897.2 F2408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:196729154 A>G maps to NM_018897.2 F2408F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:230723525 G>C maps to ENST00000389044 S330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:230723525 G>C maps to ENST00000389044 S330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:242080124 C>T maps to ENST00000358649 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr2:242080124 C>T maps to ENST00000358649 Q80Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr20:1460690 G>A maps to NM_001122962.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr20:1460690 G>A maps to NM_001122962.1 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr20:62708227 C>T maps to NM_005873.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr20:62708227 C>T maps to NM_005873.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:40182008 C>T maps to NM_005239.4 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:40182008 C>T maps to NM_005239.4 N17N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:45994408 G>A maps to NM_198687.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:45994408 G>A maps to NM_198687.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:45994441 T>C maps to NM_198687.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:45994441 T>C maps to NM_198687.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:45994612 G>C maps to NM_198687.1 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:45994612 G>C maps to NM_198687.1 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:45999840 A>G maps to NM_198694.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:45999840 A>G maps to NM_198694.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:46021228 T>C maps to ENST00000380102 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr21:46021228 T>C maps to ENST00000380102 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:16287510 G>A maps to NM_001136213.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:16287510 G>A maps to NM_001136213.1 D125D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:29885500 A>G maps to NM_021076.3 E624E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:29885500 A>G maps to NM_021076.3 E624E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:29885827 C>T maps to NM_021076.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:29885827 C>T maps to NM_021076.3 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:36055618 C>G maps to NM_030641.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:36055618 C>G maps to NM_030641.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:37266515 C>A maps to NM_013416.3 Y134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:37266515 C>A maps to NM_013416.3 Y134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:38120005 T>C maps to NM_001039141.2 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:38120005 T>C maps to NM_001039141.2 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:38369885 G>A maps to NM_006941.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr22:38369885 G>A maps to NM_006941.3 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:47958143 A>G maps to ENST00000426837 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:47958143 A>G maps to ENST00000426837 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:47958146 C>T maps to ENST00000426837 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:47958146 C>T maps to ENST00000426837 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:50310964 G>T did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:50310964 G>T did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:64084966 C>T maps to NM_198859.3 W765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:64084966 C>T maps to NM_198859.3 W765*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:97596429 C>G maps to ENST00000182096 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:97596429 C>G maps to ENST00000182096 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:129170833 G>A maps to NM_052985.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:129170833 G>A maps to NM_052985.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:183887804 C>T maps to NM_004423.3 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:183887804 C>T maps to NM_004423.3 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:188956638 G>C maps to NM_198485.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr3:188956638 G>C maps to NM_198485.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:6642971 G>C maps to NM_033296.1 *128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:6642971 G>C maps to NM_033296.1 *128S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:8230030 C>T maps to NM_018986.3 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:8230030 C>T maps to NM_018986.3 A870A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:25415343 C>T maps to ENST00000510092 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:25415343 C>T maps to ENST00000510092 Q536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:66270135 T>A maps to NM_004439.5 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:66270135 T>A maps to NM_004439.5 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:69885718 T>C maps to ENST00000381096 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:69885718 T>C maps to ENST00000381096 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:77003065 C>T maps to NM_001130016.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:77003065 C>T maps to NM_001130016.1 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:152200975 C>T maps to NM_183375.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:152200975 C>T maps to NM_183375.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:152201065 C>G maps to NM_183375.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:152201065 C>G maps to NM_183375.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:169589346 C>T maps to NM_001166108.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr4:169589346 C>T maps to NM_001166108.1 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:13762982 C>A maps to NM_001369.2 E3377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:13762982 C>A maps to NM_001369.2 E3377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:34830791 G>C did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:34830791 G>C did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:71756189 G>A maps to NM_152625.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:71756189 G>A maps to NM_152625.1 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:132222084 C>A maps to NM_014423.3 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:132222084 C>A maps to NM_014423.3 E1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:137892545 C>A maps to NM_004134.6 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:137892545 C>A maps to NM_004134.6 E580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:140531355 G>A maps to NM_018939.2 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:140531355 G>A maps to NM_018939.2 A506A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:170736612 C>T maps to NM_021025.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:170736612 C>T maps to NM_021025.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:179306152 G>A maps to NM_198868.2 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr5:179306152 G>A maps to NM_198868.2 F487F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:25727498 T>C maps to NM_170610.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:25727498 T>C maps to NM_170610.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:25727507 C>T maps to NM_170610.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:25727507 C>T maps to NM_170610.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775318 G>A maps to NM_003519.3 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775318 G>A maps to NM_003519.3 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775345 C>G maps to NM_003519.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775345 C>G maps to NM_003519.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775351 C>G maps to NM_003519.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775351 C>G maps to NM_003519.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775435 G>A maps to NM_003519.3 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775435 G>A maps to NM_003519.3 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775507 G>A maps to NM_003519.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775507 G>A maps to NM_003519.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775513 A>G maps to NM_003519.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775513 A>G maps to NM_003519.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775561 G>A maps to NM_003519.3 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775561 G>A maps to NM_003519.3 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775567 G>A maps to NM_003519.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775567 G>A maps to NM_003519.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775645 C>T maps to NM_003519.3 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27775645 C>T maps to NM_003519.3 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782158 T>C maps to NM_021066.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782158 T>C maps to NM_021066.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782164 T>G maps to NM_021066.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782164 T>G maps to NM_021066.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782170 C>T maps to NM_021066.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782170 C>T maps to NM_021066.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782937 T>C maps to NM_003521.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782937 T>C maps to NM_003521.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782943 T>C maps to NM_003521.2 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782943 T>C maps to NM_003521.2 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782991 C>T maps to NM_003521.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782991 C>T maps to NM_003521.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782997 T>C maps to NM_003521.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27782997 T>C maps to NM_003521.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27783033 T>C maps to NM_003521.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27783033 T>C maps to NM_003521.2 F71F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27783069 T>C maps to NM_003521.2 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27783069 T>C maps to NM_003521.2 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27783096 G>C maps to NM_003521.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27783096 G>C maps to NM_003521.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31118779 C>T maps to NM_001105564.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31118779 C>T maps to NM_001105564.1 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31600223 G>C maps to NM_080686.2 R1258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31600223 G>C maps to NM_080686.2 R1258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31604508 G>A did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31604508 G>A did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778228 A>G maps to NM_005527.3 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778228 A>G maps to NM_005527.3 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778276 T>C maps to NM_005527.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778276 T>C maps to NM_005527.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778285 G>C maps to NM_005527.3 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778285 G>C maps to NM_005527.3 L488L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778303 A>G maps to NM_005527.3 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778303 A>G maps to NM_005527.3 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778309 A>G maps to NM_005527.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778309 A>G maps to NM_005527.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778312 C>G maps to NM_005527.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778312 C>G maps to NM_005527.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778327 A>G maps to NM_005527.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778327 A>G maps to NM_005527.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778330 A>C maps to NM_005527.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778330 A>C maps to NM_005527.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778333 T>G maps to NM_005527.3 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778333 T>G maps to NM_005527.3 G472G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778342 T>G maps to NM_005527.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778342 T>G maps to NM_005527.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778366 A>G maps to NM_005527.3 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778366 A>G maps to NM_005527.3 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778390 C>T maps to NM_005527.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778390 C>T maps to NM_005527.3 K453K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778393 T>C maps to NM_005527.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778393 T>C maps to NM_005527.3 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778414 A>G maps to NM_005527.3 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778414 A>G maps to NM_005527.3 Y445Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778447 A>G maps to NM_005527.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778447 A>G maps to NM_005527.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778462 A>G maps to NM_005527.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778462 A>G maps to NM_005527.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778468 T>C maps to NM_005527.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778468 T>C maps to NM_005527.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778501 T>G maps to NM_005527.3 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778501 T>G maps to NM_005527.3 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778522 C>T maps to NM_005527.3 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778522 C>T maps to NM_005527.3 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778525 A>G maps to NM_005527.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778525 A>G maps to NM_005527.3 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778543 G>C maps to NM_005527.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778543 G>C maps to NM_005527.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778579 T>C maps to NM_005527.3 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778579 T>C maps to NM_005527.3 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778588 A>G maps to NM_005527.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778588 A>G maps to NM_005527.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778615 T>C maps to NM_005527.3 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778615 T>C maps to NM_005527.3 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778624 A>C maps to NM_005527.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778624 A>C maps to NM_005527.3 A375A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778633 T>G maps to NM_005527.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778633 T>G maps to NM_005527.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778636 T>C maps to NM_005527.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778636 T>C maps to NM_005527.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778639 G>A maps to NM_005527.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778639 G>A maps to NM_005527.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778666 G>C maps to NM_005527.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778666 G>C maps to NM_005527.3 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778669 A>G maps to NM_005527.3 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778669 A>G maps to NM_005527.3 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778675 T>C maps to NM_005527.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778675 T>C maps to NM_005527.3 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778693 A>C maps to NM_005527.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778693 A>C maps to NM_005527.3 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778993 T>C maps to NM_005527.3 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31778993 T>C maps to NM_005527.3 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779032 A>C maps to NM_005527.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779032 A>C maps to NM_005527.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779065 A>G maps to NM_005527.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779065 A>G maps to NM_005527.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779077 A>C maps to NM_005527.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779077 A>C maps to NM_005527.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779086 T>C maps to NM_005527.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779086 T>C maps to NM_005527.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779128 A>G maps to NM_005527.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779128 A>G maps to NM_005527.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779311 A>G maps to NM_005527.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779311 A>G maps to NM_005527.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779320 A>G maps to NM_005527.3 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779320 A>G maps to NM_005527.3 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779326 G>C maps to NM_005527.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779326 G>C maps to NM_005527.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779404 A>T maps to NM_005527.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779404 A>T maps to NM_005527.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779455 A>G maps to NM_005527.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779455 A>G maps to NM_005527.3 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779464 T>C maps to NM_005527.3 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779464 T>C maps to NM_005527.3 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779467 A>G maps to NM_005527.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779467 A>G maps to NM_005527.3 F94F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779527 A>C maps to NM_005527.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779527 A>C maps to NM_005527.3 R74R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779530 T>C maps to NM_005527.3 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779530 T>C maps to NM_005527.3 K73K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779542 A>C maps to NM_005527.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779542 A>C maps to NM_005527.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779554 G>C maps to NM_005527.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779554 G>C maps to NM_005527.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779590 A>G maps to NM_005527.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779590 A>G maps to NM_005527.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779608 T>C maps to NM_005527.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779608 T>C maps to NM_005527.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779677 C>T maps to NM_005527.3 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779677 C>T maps to NM_005527.3 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779692 A>G maps to NM_005527.3 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:31779692 A>G maps to NM_005527.3 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:41196453 T>C maps to NM_198153.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:41196453 T>C maps to NM_198153.2 G22G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:41196648 C>A maps to NM_198153.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:41196648 C>A maps to NM_198153.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:133138133 C>G maps to NM_001016.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:133138133 C>G maps to NM_001016.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:151673275 G>T maps to NM_005100.3 V1250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:151673275 G>T maps to NM_005100.3 V1250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:1590519 G>A maps to NM_001097620.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:1590519 G>A maps to NM_001097620.1 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:99091154 T>C maps to NM_032164.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:99091154 T>C maps to NM_032164.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:143826825 G>A maps to NM_001001659.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:143826825 G>A maps to NM_001001659.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:143826852 C>T maps to NM_001001659.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:143826852 C>T maps to NM_001001659.1 S216S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:143826894 G>C maps to NM_001001659.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:143826894 G>C maps to NM_001001659.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:143826918 C>T maps to NM_001001659.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:143826918 C>T maps to NM_001001659.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:143826936 T>C maps to NM_001001659.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:143826936 T>C maps to NM_001001659.1 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:150439469 T>C maps to ENST00000447239 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:150439469 T>C maps to ENST00000447239 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:150439763 G>A maps to ENST00000447239 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr7:150439763 G>A maps to ENST00000447239 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr8:10465196 A>T maps to NM_178857.5 A2137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr8:10465196 A>T maps to NM_178857.5 A2137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr8:67591972 G>C maps to NM_019607.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr8:67591972 G>C maps to NM_019607.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr8:120977639 C>T maps to NM_022783.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr8:120977639 C>T maps to NM_022783.2 I198I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr8:122641223 G>C maps to NM_005328.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr8:122641223 G>C maps to NM_005328.2 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:33798036 T>C maps to NM_007343.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:33798036 T>C maps to NM_007343.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:86530260 G>C maps to NM_017576.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:86530260 G>C maps to NM_017576.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:95077985 T>C maps to NM_017948.5 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:95077985 T>C maps to NM_017948.5 E307E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:116357877 G>A did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:116357877 G>A did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:125391688 C>G maps to NM_001004450.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:125391688 C>G maps to NM_001004450.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:130416008 C>T maps to NM_003165.3 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:130416008 C>T maps to NM_003165.3 Q35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:130674557 C>T maps to NM_175039.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:130674557 C>T maps to NM_175039.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:130674581 G>A maps to NM_175039.3 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:130674581 G>A maps to NM_175039.3 C192C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:131190593 C>T maps to NM_016174.4 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:131190593 C>T maps to NM_016174.4 H260H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:135251334 A>G maps to NM_007344.2 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:135251334 A>G maps to NM_007344.2 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:135985720 G>A maps to NM_006266.2 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:135985720 G>A maps to NM_006266.2 F150F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:139276444 C>G maps to NM_003086.2 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr9:139276444 C>G maps to NM_003086.2 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:1428368 C>A maps to NM_001161530.1 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:1428368 C>A maps to NM_001161530.1 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:5821893 C>T maps to ENST00000381093 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:5821893 C>T maps to ENST00000381093 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:24228685 C>T maps to NM_003410.3 H537H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:24228685 C>T maps to NM_003410.3 H537H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:24329439 G>A maps to NM_001136233.1 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:24329439 G>A maps to NM_001136233.1 Q665*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:48759679 C>A maps to NM_005710.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:48759679 C>A maps to NM_005710.2 R155R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:101382149 A>G maps to NM_080390.3 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:101382149 A>G maps to NM_080390.3 G116G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:111155737 G>C maps to NM_012471.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:111155737 G>C maps to NM_012471.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134156270 C>T maps to NM_001078173.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134156270 C>T maps to NM_001078173.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134156387 A>G maps to NM_001078173.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134156387 A>G maps to NM_001078173.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134156435 G>A maps to NM_001078173.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134156435 G>A maps to NM_001078173.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134156477 T>C maps to NM_001078173.1 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134156477 T>C maps to NM_001078173.1 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134166514 C>T maps to NM_001078171.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134166514 C>T maps to NM_001078171.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134166529 A>G maps to NM_001078171.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134166529 A>G maps to NM_001078171.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134185913 T>G maps to NM_001078172.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:134185913 T>G maps to NM_001078172.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:135427880 C>A maps to NM_153834.3 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:135427880 C>A maps to NM_153834.3 T672T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:139586070 G>A maps to NM_005634.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:139586070 G>A maps to NM_005634.2 I385I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900052 A>G maps to NM_005367.5 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900052 A>G maps to NM_005367.5 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900110 T>C maps to NM_005367.5 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900110 T>C maps to NM_005367.5 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900356 A>G maps to NM_005367.5 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900356 A>G maps to NM_005367.5 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900521 T>C maps to NM_005367.5 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900521 T>C maps to NM_005367.5 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900563 G>A maps to NM_005367.5 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900563 G>A maps to NM_005367.5 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900569 A>G maps to NM_005367.5 Y77Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900569 A>G maps to NM_005367.5 Y77Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900683 G>A maps to NM_005367.5 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900683 G>A maps to NM_005367.5 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900686 A>G maps to NM_005367.5 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900686 A>G maps to NM_005367.5 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900727 A>G maps to NM_005367.5 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900727 A>G maps to NM_005367.5 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900761 C>T maps to NM_005367.5 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151900761 C>T maps to NM_005367.5 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:55075035 A>G maps to NM_176782.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:55075035 A>G maps to NM_176782.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858562 C>T maps to NM_003517.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858562 C>T maps to NM_003517.2 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858592 C>T maps to NM_003517.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858592 C>T maps to NM_003517.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858607 A>G maps to NM_003517.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858607 A>G maps to NM_003517.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858655 G>C maps to NM_003517.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858655 G>C maps to NM_003517.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858661 C>A maps to NM_003517.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858661 C>A maps to NM_003517.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858706 C>G maps to NM_003517.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858706 C>G maps to NM_003517.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858709 G>A maps to NM_003517.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858709 G>A maps to NM_003517.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858712 C>T maps to NM_003517.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858712 C>T maps to NM_003517.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858802 A>G maps to NM_003517.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858802 A>G maps to NM_003517.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858805 G>C maps to NM_003517.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149858805 G>C maps to NM_003517.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859277 A>G maps to NM_175065.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859277 A>G maps to NM_175065.2 I63I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859280 T>C maps to NM_175065.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859280 T>C maps to NM_175065.2 E62E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859283 C>G maps to NM_175065.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859283 C>G maps to NM_175065.2 A61A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859328 T>G maps to NM_175065.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859328 T>G maps to NM_175065.2 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859334 G>C maps to NM_175065.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859334 G>C maps to NM_175065.2 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859382 C>T maps to NM_175065.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859382 C>T maps to NM_175065.2 V28V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859397 A>G maps to NM_175065.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:149859397 A>G maps to NM_175065.2 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152327210 A>T maps to NM_001014342.2 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152327210 A>T maps to NM_001014342.2 S1017S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152327606 T>G maps to NM_001014342.2 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152327606 T>G maps to NM_001014342.2 G885G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152327897 A>T maps to NM_001014342.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152327897 A>T maps to NM_001014342.2 S788S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152328221 A>G maps to NM_001014342.2 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152328221 A>G maps to NM_001014342.2 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152328281 T>C maps to NM_001014342.2 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152328281 T>C maps to NM_001014342.2 S660S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152759891 A>T maps to ENST00000417924 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152759891 A>T maps to ENST00000417924 P35P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152770350 T>A maps to NM_178352.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152770350 T>A maps to NM_178352.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152770353 A>G maps to NM_178352.2 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152770353 A>G maps to NM_178352.2 K28K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152777598 C>T maps to NM_178351.3 *119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152777598 C>T maps to NM_178351.3 *119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152777756 T>A maps to NM_178351.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152777756 T>A maps to NM_178351.3 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152785277 A>G maps to NM_178349.1 *119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:152785277 A>G maps to NM_178349.1 *119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:197071243 C>T maps to NM_018136.4 Q2379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:197071243 C>T maps to NM_018136.4 Q2379Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:228645895 A>G maps to NM_175055.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:228645895 A>G maps to NM_175055.2 A22A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:228646126 T>G maps to NM_175055.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr1:228646126 T>G maps to NM_175055.2 V99V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr10:81373616 A>T maps to NM_001093770.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr10:81373616 A>T maps to NM_001093770.2 P180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:308197 C>T maps to NM_006435.2 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:308197 C>T maps to NM_006435.2 N2N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:308206 G>C maps to NM_006435.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:308206 G>C maps to NM_006435.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:315008 C>T maps to ENST00000328221 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:315008 C>T maps to ENST00000328221 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1642783 G>A maps to NM_001012709.1 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1642783 G>A maps to NM_001012709.1 C180C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1643278 C>T maps to ENST00000359229 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1643278 C>T maps to ENST00000359229 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1643368 T>G did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1643368 T>G did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1651090 C>T maps to NM_001001480.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1651090 C>T maps to NM_001001480.2 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1651441 G>T maps to NM_001001480.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1651441 G>T maps to NM_001001480.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1651471 G>T maps to NM_001001480.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1651471 G>T maps to NM_001001480.2 G134G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1651759 C>T maps to NM_001001480.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:1651759 C>T maps to NM_001001480.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:6790074 T>G maps to NM_001004490.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:6790074 T>G maps to NM_001004490.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:55861592 G>A maps to NM_001003750.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:55861592 G>A maps to NM_001003750.1 A270A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57970927 T>A maps to NM_001004459.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57970927 T>A maps to NM_001004459.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57971143 A>C maps to NM_001004459.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57971143 A>C maps to NM_001004459.1 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57971419 G>A maps to NM_001004459.1 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57971419 G>A maps to NM_001004459.1 Y78Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57971446 G>A maps to NM_001004459.1 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57971446 G>A maps to NM_001004459.1 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57971563 G>A maps to NM_001004459.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57971563 G>A maps to NM_001004459.1 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982320 G>A maps to NM_001004458.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982320 G>A maps to NM_001004458.1 E35E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982422 T>C maps to NM_001004458.1 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982422 T>C maps to NM_001004458.1 H69H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982449 T>C maps to NM_001004458.1 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982449 T>C maps to NM_001004458.1 N78N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982521 T>C maps to NM_001004458.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982521 T>C maps to NM_001004458.1 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982596 C>T maps to NM_001004458.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982596 C>T maps to NM_001004458.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982647 T>C maps to NM_001004458.1 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982647 T>C maps to NM_001004458.1 N144N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982698 A>G maps to NM_001004458.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982698 A>G maps to NM_001004458.1 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982902 T>C maps to NM_001004458.1 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982902 T>C maps to NM_001004458.1 F229F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982941 T>A maps to NM_001004458.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:57982941 T>A maps to NM_001004458.1 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71276935 G>A maps to ENST00000422553 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71276935 G>A maps to ENST00000422553 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71277139 G>A maps to NM_001012710.1 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71277139 G>A maps to NM_001012710.1 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71277196 T>C maps to NM_001012710.1 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71277196 T>C maps to NM_001012710.1 C188C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71293457 G>A maps to ENST00000376535 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71293457 G>A maps to ENST00000376535 C142C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71293625 G>A maps to ENST00000376535 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71293625 G>A maps to ENST00000376535 N86N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71293847 A>G maps to ENST00000376535 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:71293847 A>G maps to ENST00000376535 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123900634 C>T maps to NM_001004464.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123900634 C>T maps to NM_001004464.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123900637 T>C maps to NM_001004464.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123900637 T>C maps to NM_001004464.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123900751 T>C maps to ENST00000375021 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123900751 T>C maps to ENST00000375021 T141T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123900964 G>C maps to ENST00000375021 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123900964 G>C maps to ENST00000375021 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123901198 G>A maps to ENST00000375021 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123901198 G>A maps to ENST00000375021 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123901210 G>A maps to ENST00000375021 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123901210 G>A maps to ENST00000375021 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123908826 T>C maps to NM_001004463.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123908826 T>C maps to NM_001004463.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123908838 T>C maps to NM_001004463.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123908838 T>C maps to NM_001004463.1 R290R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123909399 G>A maps to NM_001004463.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123909399 G>A maps to NM_001004463.1 F103F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123909402 A>G maps to NM_001004463.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:123909402 A>G maps to NM_001004463.1 F102F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:124740157 T>C maps to NM_022370.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr11:124740157 T>C maps to NM_022370.3 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:6981744 G>A maps to NM_032641.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:6981744 G>A maps to NM_032641.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:33535417 T>A maps to NM_198992.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:33535417 T>A maps to NM_198992.3 R412R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52681013 G>A maps to NM_002281.3 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52681013 G>A maps to NM_002281.3 G373G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52681088 G>A maps to NM_002281.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52681088 G>A maps to NM_002281.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52681103 G>A maps to NM_002281.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52681103 G>A maps to NM_002281.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52695726 C>G maps to NM_002284.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52695726 C>G maps to NM_002284.3 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52699466 G>A maps to NM_002284.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52699466 G>A maps to NM_002284.3 T307T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52709723 A>G maps to NM_002282.3 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52709723 A>G maps to NM_002282.3 D405D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52710275 G>A maps to NM_002282.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52710275 G>A maps to NM_002282.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52710278 T>C maps to NM_002282.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52710278 T>C maps to NM_002282.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52710356 T>C maps to NM_002282.3 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:52710356 T>C maps to NM_002282.3 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:125397434 G>A maps to NM_021009.5 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:125397434 G>A maps to NM_021009.5 L295L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:125397489 C>T maps to NM_021009.5 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr12:125397489 C>T maps to NM_021009.5 K276K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr13:25744293 G>C maps to NM_152704.2 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr13:25744293 G>C maps to NM_152704.2 V488V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr13:58208140 G>A maps to NM_001040429.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr13:58208140 G>A maps to NM_001040429.2 P487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr13:67802143 T>C maps to NM_203487.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr13:67802143 T>C maps to NM_203487.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr14:52156574 T>C maps to ENST00000344768 H7H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr14:52156574 T>C maps to ENST00000344768 H7H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr15:45668876 G>A maps to ENST00000432007 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr15:45668876 G>A maps to ENST00000432007 N123N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:1306556 G>T maps to NM_012217.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:1306556 G>T maps to NM_012217.2 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063539 G>C maps to NM_020982.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063539 G>C maps to NM_020982.3 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063578 T>G maps to NM_020982.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063578 T>G maps to NM_020982.3 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063599 C>T maps to NM_020982.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063599 C>T maps to NM_020982.3 A79A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063767 T>C maps to NM_020982.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063767 T>C maps to NM_020982.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063785 C>T maps to NM_020982.3 H141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063785 C>T maps to NM_020982.3 H141H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063806 C>T maps to NM_020982.3 Y148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063806 C>T maps to NM_020982.3 Y148Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063858 C>T maps to NM_020982.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3063858 C>T maps to NM_020982.3 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3065704 G>C maps to NM_021195.4 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3065704 G>C maps to NM_021195.4 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3065806 C>A maps to NM_021195.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3065806 C>A maps to NM_021195.4 A72A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3065845 G>C maps to NM_021195.4 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3065845 G>C maps to NM_021195.4 T59T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3065920 A>G maps to NM_021195.4 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:3065920 A>G maps to NM_021195.4 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:20857562 G>A maps to NM_030941.2 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:20857562 G>A maps to NM_030941.2 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:31374541 T>C maps to NM_000887.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:31374541 T>C maps to NM_000887.3 G519G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:31374553 G>A maps to NM_000887.3 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:31374553 G>A maps to NM_000887.3 A523A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:56700868 G>A maps to ENST00000379811 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:56700868 G>A maps to ENST00000379811 C37C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:56704873 G>A maps to NM_005951.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:56704873 G>A maps to NM_005951.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:56704876 A>G maps to NM_005951.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:56704876 A>G maps to NM_005951.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:56704894 T>C maps to NM_005951.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:56704894 T>C maps to NM_005951.2 C60C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:84806241 G>A maps to NM_005153.2 Q698Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr16:84806241 G>A maps to NM_005153.2 Q698Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39254276 G>A maps to NM_031960.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39254276 G>A maps to NM_031960.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39254291 A>G maps to NM_031960.2 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39254291 A>G maps to NM_031960.2 C15C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39254297 T>C maps to NM_031960.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39254297 T>C maps to NM_031960.2 Q13Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39261777 A>G maps to NM_001146041.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39261777 A>G maps to NM_001146041.1 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39279993 T>C maps to NM_031854.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39279993 T>C maps to NM_031854.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39280113 T>C maps to NM_031854.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39280113 T>C maps to NM_031854.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39394317 T>C maps to NM_031963.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:39394317 T>C maps to NM_031963.2 C5C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:7810452 A>G maps to NM_021155.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:7810452 A>G maps to NM_021155.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:7810533 A>C maps to NM_021155.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:7810533 A>C maps to NM_021155.3 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:7810797 A>G maps to NM_021155.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:7810797 A>G maps to NM_021155.3 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:7810809 A>C maps to NM_021155.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:7810809 A>C maps to NM_021155.3 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:7830974 C>T maps to NM_014257.4 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:7830974 C>T maps to NM_014257.4 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:15918655 G>A maps to NM_013940.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:15918655 G>A maps to NM_013940.2 C64C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:21720804 T>C maps to NM_001001415.2 H650H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:21720804 T>C maps to NM_001001415.2 H650H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:23836897 T>A maps to NM_138330.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:23836897 T>A maps to NM_138330.2 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:36352021 A>G did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:36352021 A>G did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:44636230 A>G maps to NM_013362.2 E488E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:44636230 A>G maps to NM_013362.2 E488E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:44778318 T>C maps to NM_181756.1 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:44778318 T>C maps to NM_181756.1 H502H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:46444089 C>T maps to NM_002516.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:46444089 C>T maps to NM_002516.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:49536438 A>T maps to NM_033378.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:49536438 A>T maps to NM_033378.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:50461720 C>A maps to NM_052884.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:50461720 C>A maps to NM_052884.2 G490G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:50462083 G>T maps to NM_052884.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:50462083 G>T maps to NM_052884.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:53644379 T>C maps to NM_001172674.1 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:53644379 T>C maps to NM_001172674.1 K568K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:53762440 T>G maps to NM_173856.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:53762440 T>G maps to NM_173856.2 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:53856693 A>G maps to NM_138374.1 K922K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:53856693 A>G maps to NM_138374.1 K922K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:53958987 T>C maps to NM_001008401.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:53958987 T>C maps to NM_001008401.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:53994379 T>C maps to NM_001004301.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:53994379 T>C maps to NM_001004301.3 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56701531 T>C maps to NM_001080456.2 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56701531 T>C maps to NM_001080456.2 Q384Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56701663 C>T maps to NM_001080456.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56701663 C>T maps to NM_001080456.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56733045 G>A maps to NM_024303.1 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56733045 G>A maps to NM_024303.1 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56733267 A>G maps to NM_024303.1 C389C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56733267 A>G maps to NM_024303.1 C389C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56733279 T>C maps to NM_024303.1 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56733279 T>C maps to NM_024303.1 Q385Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56733525 A>G maps to NM_024303.1 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56733525 A>G maps to NM_024303.1 D303D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56734026 A>G maps to NM_024303.1 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56734026 A>G maps to NM_024303.1 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56735083 C>A maps to NM_024303.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56735083 C>A maps to NM_024303.1 S168S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56736334 T>A maps to NM_024303.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:56736334 T>A maps to NM_024303.1 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:58199409 T>C maps to ENST00000356715 C589C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr19:58199409 T>C maps to ENST00000356715 C589C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr2:37076667 T>C maps to NM_003162.2 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr2:37076667 T>C maps to NM_003162.2 V758V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr20:23546709 A>G maps to NM_080610.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr20:23546709 A>G maps to NM_080610.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr20:62708227 C>T maps to NM_005873.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr20:62708227 C>T maps to NM_005873.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:31798175 A>G maps to NM_181622.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:31798175 A>G maps to NM_181622.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45994249 G>A maps to NM_198687.1 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45994249 G>A maps to NM_198687.1 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45994408 G>A maps to NM_198687.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45994408 G>A maps to NM_198687.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45994441 T>C maps to NM_198687.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45994441 T>C maps to NM_198687.1 A269A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45994594 C>T maps to NM_198687.1 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45994594 C>T maps to NM_198687.1 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45994738 G>A maps to NM_198687.1 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45994738 G>A maps to NM_198687.1 V368V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45999693 C>T maps to NM_198694.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45999693 C>T maps to NM_198694.2 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45999840 A>G maps to NM_198694.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:45999840 A>G maps to NM_198694.2 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:46011435 A>G maps to NM_198688.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:46011435 A>G maps to NM_198688.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:46011525 T>A maps to NM_198688.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:46011525 T>A maps to NM_198688.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:46021150 G>A maps to ENST00000380102 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:46021150 G>A maps to ENST00000380102 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:46021228 T>C maps to ENST00000380102 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:46021228 T>C maps to ENST00000380102 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:46021414 C>T maps to ENST00000380102 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr21:46021414 C>T maps to ENST00000380102 C298C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr22:29754807 G>A maps to NM_001127.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr22:29754807 G>A maps to NM_001127.3 C144C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr22:36892229 C>A maps to NM_001102371.1 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr22:36892229 C>A maps to NM_001102371.1 E470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr22:38120005 T>C maps to NM_001039141.2 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr22:38120005 T>C maps to NM_001039141.2 C481C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr22:38120668 A>G maps to NM_001039141.2 Q702Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr22:38120668 A>G maps to NM_001039141.2 Q702Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr3:47958143 A>G maps to ENST00000426837 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr3:47958143 A>G maps to ENST00000426837 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr3:47958146 C>T maps to ENST00000426837 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr3:47958146 C>T maps to ENST00000426837 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr3:123419188 C>T maps to NM_053025.3 K1042K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr3:123419188 C>T maps to NM_053025.3 K1042K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:366981 A>G maps to NM_003441.2 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:366981 A>G maps to NM_003441.2 E252E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:436173 T>C maps to NM_133474.2 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:436173 T>C maps to NM_133474.2 E694E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:68784829 G>A maps to NM_182606.3 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:68784829 G>A maps to NM_182606.3 Y274Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:69885790 T>C maps to ENST00000381096 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:69885790 T>C maps to ENST00000381096 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:69885793 A>G maps to ENST00000381096 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:69885793 A>G maps to ENST00000381096 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:70361516 C>T maps to NM_021139.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:70361516 C>T maps to NM_021139.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:152201065 C>G maps to NM_183375.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr4:152201065 C>G maps to NM_183375.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr5:68660802 G>A maps to NM_001015892.1 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr5:68660802 G>A maps to NM_001015892.1 D254D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775318 G>A maps to NM_003519.3 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775318 G>A maps to NM_003519.3 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775345 C>G maps to NM_003519.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775345 C>G maps to NM_003519.3 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775351 C>G maps to NM_003519.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775351 C>G maps to NM_003519.3 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775365 G>A maps to NM_003519.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775365 G>A maps to NM_003519.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775408 G>C maps to NM_003519.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775408 G>C maps to NM_003519.3 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775411 G>A maps to NM_003519.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775411 G>A maps to NM_003519.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775507 G>A maps to NM_003519.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775507 G>A maps to NM_003519.3 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775513 A>G maps to NM_003519.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775513 A>G maps to NM_003519.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775561 G>A maps to NM_003519.3 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775561 G>A maps to NM_003519.3 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775567 G>A maps to NM_003519.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775567 G>A maps to NM_003519.3 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775645 C>T maps to NM_003519.3 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27775645 C>T maps to NM_003519.3 K13K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782155 A>G maps to NM_021066.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782155 A>G maps to NM_021066.2 T121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782158 T>C maps to NM_021066.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782158 T>C maps to NM_021066.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782164 T>G maps to NM_021066.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782164 T>G maps to NM_021066.2 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782170 C>T maps to NM_021066.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782170 C>T maps to NM_021066.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782937 T>C maps to NM_003521.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782937 T>C maps to NM_003521.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782943 T>C maps to NM_003521.2 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782943 T>C maps to NM_003521.2 Y41Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782991 C>T maps to NM_003521.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782991 C>T maps to NM_003521.2 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782997 T>C maps to NM_003521.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27782997 T>C maps to NM_003521.2 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783039 T>C maps to NM_003521.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783039 T>C maps to NM_003521.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783069 T>C maps to NM_003521.2 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783069 T>C maps to NM_003521.2 H83H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783093 T>C maps to NM_003521.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783093 T>C maps to NM_003521.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783096 G>C maps to NM_003521.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783096 G>C maps to NM_003521.2 S92S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783111 G>C maps to NM_003521.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783111 G>C maps to NM_003521.2 T97T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783186 T>C maps to NM_003521.2 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27783186 T>C maps to NM_003521.2 Y122Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:30955190 G>C maps to NM_001010909.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:30955190 G>C maps to NM_001010909.2 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778228 A>G maps to NM_005527.3 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778228 A>G maps to NM_005527.3 N507N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778276 T>C maps to NM_005527.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778276 T>C maps to NM_005527.3 T491T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778288 A>G maps to NM_005527.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778288 A>G maps to NM_005527.3 I487I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778303 A>G maps to NM_005527.3 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778303 A>G maps to NM_005527.3 I482I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778309 A>G maps to NM_005527.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778309 A>G maps to NM_005527.3 F480F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778312 C>G maps to NM_005527.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778312 C>G maps to NM_005527.3 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778327 A>G maps to NM_005527.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778327 A>G maps to NM_005527.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778330 A>C maps to NM_005527.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778330 A>C maps to NM_005527.3 V473V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778342 T>G maps to NM_005527.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778342 T>G maps to NM_005527.3 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778366 A>G maps to NM_005527.3 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778366 A>G maps to NM_005527.3 F461F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778369 C>G maps to NM_005527.3 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778369 C>G maps to NM_005527.3 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778447 A>G maps to NM_005527.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778447 A>G maps to NM_005527.3 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778462 A>G maps to NM_005527.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778462 A>G maps to NM_005527.3 I429I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778468 T>C maps to NM_005527.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778468 T>C maps to NM_005527.3 T427T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778501 T>G maps to NM_005527.3 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778501 T>G maps to NM_005527.3 I416I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778522 C>T maps to NM_005527.3 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778522 C>T maps to NM_005527.3 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778543 G>C maps to NM_005527.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778543 G>C maps to NM_005527.3 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778579 T>C maps to NM_005527.3 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778579 T>C maps to NM_005527.3 V390V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778588 A>G maps to NM_005527.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778588 A>G maps to NM_005527.3 S387S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778612 T>C maps to NM_005527.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778612 T>C maps to NM_005527.3 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778615 T>C maps to NM_005527.3 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778615 T>C maps to NM_005527.3 Q378Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778618 T>C maps to NM_005527.3 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778618 T>C maps to NM_005527.3 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778636 T>C maps to NM_005527.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778636 T>C maps to NM_005527.3 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778639 G>A maps to NM_005527.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778639 G>A maps to NM_005527.3 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778669 A>G maps to NM_005527.3 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778669 A>G maps to NM_005527.3 D360D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778861 A>G maps to NM_005527.3 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778861 A>G maps to NM_005527.3 Y296Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778993 T>C maps to NM_005527.3 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31778993 T>C maps to NM_005527.3 K252K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779032 A>C maps to NM_005527.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779032 A>C maps to NM_005527.3 L239L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779065 A>G maps to NM_005527.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779065 A>G maps to NM_005527.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779074 A>G maps to NM_005527.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779074 A>G maps to NM_005527.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779077 A>C maps to NM_005527.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779077 A>C maps to NM_005527.3 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779086 T>C maps to NM_005527.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779086 T>C maps to NM_005527.3 V221V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779119 T>G maps to NM_005527.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779119 T>G maps to NM_005527.3 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779230 T>C maps to NM_005527.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779230 T>C maps to NM_005527.3 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779317 T>C maps to NM_005527.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779317 T>C maps to NM_005527.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779326 G>C maps to NM_005527.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779326 G>C maps to NM_005527.3 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779350 A>G maps to NM_005527.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779350 A>G maps to NM_005527.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779395 A>G maps to NM_005527.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779395 A>G maps to NM_005527.3 P118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779464 T>C maps to NM_005527.3 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779464 T>C maps to NM_005527.3 Q95Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779590 A>G maps to NM_005527.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779590 A>G maps to NM_005527.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779608 T>C maps to NM_005527.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779608 T>C maps to NM_005527.3 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779677 C>T maps to NM_005527.3 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779677 C>T maps to NM_005527.3 Q24Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779692 A>G maps to NM_005527.3 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:31779692 A>G maps to NM_005527.3 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:41196605 G>A maps to NM_198153.2 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:41196605 G>A maps to NM_198153.2 W73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:41196648 C>A maps to NM_198153.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:41196648 C>A maps to NM_198153.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:133138133 C>G maps to NM_001016.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:133138133 C>G maps to NM_001016.3 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:44146298 T>C maps to NM_001129.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:44146298 T>C maps to NM_001129.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:99091154 T>C maps to NM_032164.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:99091154 T>C maps to NM_032164.2 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:100350604 A>G maps to ENST00000349350 T959T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:100350604 A>G maps to ENST00000349350 T959T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:121942299 G>T maps to NM_001024613.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:121942299 G>T maps to NM_001024613.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:143826877 T>C maps to NM_001001659.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:143826877 T>C maps to NM_001001659.1 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:143826894 G>C maps to NM_001001659.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:143826894 G>C maps to NM_001001659.1 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:143826918 C>T maps to NM_001001659.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:143826918 C>T maps to NM_001001659.1 S238S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:143827002 T>C maps to NM_001001659.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:143827002 T>C maps to NM_001001659.1 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:150439433 A>G maps to ENST00000447239 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:150439433 A>G maps to ENST00000447239 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:150439448 C>T maps to ENST00000447239 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:150439448 C>T maps to ENST00000447239 N110N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:150864161 C>T maps to NM_001098834.1 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr7:150864161 C>T maps to NM_001098834.1 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr8:24775224 A>G maps to NM_005382.2 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr8:24775224 A>G maps to NM_005382.2 K619K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr8:24775338 G>C maps to NM_005382.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr8:24775338 G>C maps to NM_005382.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr8:24775341 A>G maps to NM_005382.2 K658K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr8:24775341 A>G maps to NM_005382.2 K658K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr8:67590056 A>G maps to NM_019607.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr8:67590056 A>G maps to NM_019607.1 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr9:130674557 C>T maps to NM_175039.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr9:130674557 C>T maps to NM_175039.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr9:135251334 A>G maps to NM_007344.2 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr9:135251334 A>G maps to NM_007344.2 S895S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:46332200 T>C maps to NM_001129898.1 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:46332200 T>C maps to NM_001129898.1 D90D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:48125806 G>A maps to NM_005635.2 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:48125806 G>A maps to NM_005635.2 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:48209527 T>C maps to NM_021014.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:48209527 T>C maps to NM_021014.2 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:99854094 A>G maps to NM_022144.2 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:99854094 A>G maps to NM_022144.2 E220E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:100871235 C>T maps to NM_019007.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:100871235 C>T maps to NM_019007.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:102968619 G>C maps to NM_182541.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:102968619 G>C maps to NM_182541.2 T67T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134156270 C>T maps to NM_001078173.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134156270 C>T maps to NM_001078173.1 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134156387 A>G maps to NM_001078173.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134156387 A>G maps to NM_001078173.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134166466 T>C maps to NM_001078171.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134166466 T>C maps to NM_001078171.1 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134166514 C>T maps to NM_001078171.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134166514 C>T maps to NM_001078171.1 D34D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134166529 A>G maps to NM_001078171.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134166529 A>G maps to NM_001078171.1 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134303553 T>C maps to NM_001031705.2 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:134303553 T>C maps to NM_001031705.2 E81E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900052 A>G maps to NM_005367.5 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900052 A>G maps to NM_005367.5 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900110 T>C maps to NM_005367.5 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900110 T>C maps to NM_005367.5 A230A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900356 A>G maps to NM_005367.5 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900356 A>G maps to NM_005367.5 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900521 T>C maps to NM_005367.5 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900521 T>C maps to NM_005367.5 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900623 T>C maps to NM_005367.5 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900623 T>C maps to NM_005367.5 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900656 G>A maps to NM_005367.5 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900656 G>A maps to NM_005367.5 V48V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900680 G>A maps to NM_005367.5 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900680 G>A maps to NM_005367.5 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900683 G>A maps to NM_005367.5 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900683 G>A maps to NM_005367.5 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900686 A>G maps to NM_005367.5 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900686 A>G maps to NM_005367.5 T38T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900727 A>G maps to NM_005367.5 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900727 A>G maps to NM_005367.5 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900761 C>T maps to NM_005367.5 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151900761 C>T maps to NM_005367.5 E13E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:153033840 C>T maps to NM_005393.2 H408H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:153033840 C>T maps to NM_005393.2 H408H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr1:173839497 T>C maps to NM_001122770.1 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr1:173839497 T>C maps to NM_001122770.1 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr10:38403717 C>T maps to NM_003421.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr10:38403717 C>T maps to NM_003421.2 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr10:72434399 G>A maps to NM_139155.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr10:72434399 G>A maps to NM_139155.2 V57V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr10:111987977 G>A maps to NM_130439.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr10:111987977 G>A maps to NM_130439.3 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr11:1078303 G>A maps to ENST00000441003 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr11:1078303 G>A maps to ENST00000441003 Q197Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr11:30034063 G>A maps to NM_002233.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr11:30034063 G>A maps to NM_002233.2 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr11:56344765 C>A maps to NM_001004741.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr11:56344765 C>A maps to NM_001004741.1 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr12:57559990 A>G maps to NM_002332.2 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr12:57559990 A>G maps to NM_002332.2 S932S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr13:67800079 G>A maps to NM_203487.2 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr13:67800079 G>A maps to NM_203487.2 F831F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr15:90770836 C>T maps to NM_198925.2 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr15:90770836 C>T maps to NM_198925.2 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr16:55886940 C>T did not map to a codon.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr16:55886940 C>T did not map to a codon.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr17:4098306 G>A maps to NM_016376.3 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr17:4098306 G>A maps to NM_016376.3 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr17:39274156 G>A maps to NM_033059.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr17:39274156 G>A maps to NM_033059.3 P137P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr19:17108022 G>A maps to ENST00000443236 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr19:17108022 G>A maps to ENST00000443236 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr19:23542270 C>T maps to NM_003430.2 A1170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr19:23542270 C>T maps to NM_003430.2 A1170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr2:193059223 C>T maps to NM_016192.2 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr2:193059223 C>T maps to NM_016192.2 Q9Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr3:196304664 C>T maps to NM_001105573.1 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr3:196304664 C>T maps to NM_001105573.1 N220N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr5:41176762 T>A maps to NM_001115131.1 K328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr5:41176762 T>A maps to NM_001115131.1 K328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr5:176687058 C>G maps to NM_022455.4 S1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr5:176687058 C>G maps to NM_022455.4 S1679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr7:100732122 C>T maps to NM_030961.1 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr7:100732122 C>T maps to NM_030961.1 I510I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr8:11162519 G>A maps to NM_015458.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr8:11162519 G>A maps to NM_015458.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr8:53092775 G>C maps to NM_014682.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr8:53092775 G>C maps to NM_014682.2 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr8:82586094 T>C maps to NM_001144878.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EA-A1QT-01A-11D-A14W-08 chr8:82586094 T>C maps to NM_001144878.1 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:10699535 C>T maps to NM_001079843.1 T1581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:10699535 C>T maps to NM_001079843.1 T1581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:29314293 G>A maps to NM_001166005.1 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:29314293 G>A maps to NM_001166005.1 E115E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:162737061 T>C maps to NM_006182.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:162737061 T>C maps to NM_006182.2 I402I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:204408074 G>A maps to NM_002646.3 D1168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:204408074 G>A maps to NM_002646.3 D1168D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:223176988 C>T maps to NM_032890.2 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:223176988 C>T maps to NM_032890.2 S750S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr10:38343651 G>A maps to NM_006954.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr10:38343651 G>A maps to NM_006954.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr11:7647009 T>C maps to NM_003621.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr11:7647009 T>C maps to NM_003621.2 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr11:62455620 G>A maps to NM_203422.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr11:62455620 G>A maps to NM_203422.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr12:4870146 C>T maps to NM_017417.1 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr12:4870146 C>T maps to NM_017417.1 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr15:44127314 C>T maps to NM_024908.3 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr15:44127314 C>T maps to NM_024908.3 N173N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr16:1810462 T>C maps to NM_015133.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr16:1810462 T>C maps to NM_015133.3 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr17:39643887 G>A maps to NM_003771.4 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr17:39643887 G>A maps to NM_003771.4 C267C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr18:34376836 T>G maps to NM_015476.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr18:34376836 T>G maps to NM_015476.2 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr2:113955394 C>T maps to NM_012455.2 H843H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr2:113955394 C>T maps to NM_012455.2 H843H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr3:169802323 C>T maps to NM_014373.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr3:169802323 C>T maps to NM_014373.2 F188F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr4:144359595 G>A maps to NM_207123.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr4:144359595 G>A maps to NM_207123.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr5:96322253 C>T maps to NM_005575.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr5:96322253 C>T maps to NM_005575.2 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr6:33148096 G>A maps to NM_080680.2 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr6:33148096 G>A maps to NM_080680.2 R433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr6:130399705 T>C maps to NM_032438.2 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr6:130399705 T>C maps to NM_032438.2 C416C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr6:152647695 C>A maps to NM_182961.2 E5010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr6:152647695 C>A maps to NM_182961.2 E5010*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr8:28218545 T>G maps to NM_018660.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr8:28218545 T>G maps to NM_018660.2 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr9:35752744 G>A maps to ENST00000456972 W390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr9:35752744 G>A maps to ENST00000456972 W390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chrX:133549135 C>T maps to ENST00000394292 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chrX:133549135 C>T maps to ENST00000394292 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chrX:150841058 G>A maps to NM_173493.2 Q614Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chrX:150841058 G>A maps to NM_173493.2 Q614Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:17285208 G>A maps to NM_014675.3 L1332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:17285208 G>A maps to NM_014675.3 L1332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:19204080 G>A maps to NM_003748.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:19204080 G>A maps to NM_003748.3 F322F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:43665155 G>C maps to NM_001195831.1 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:43665155 G>C maps to NM_001195831.1 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:52882346 G>C maps to NM_032864.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:52882346 G>C maps to NM_032864.3 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:169677747 T>G maps to NM_000655.4 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:169677747 T>G maps to NM_000655.4 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:220269458 C>A maps to NM_018060.3 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr1:220269458 C>A maps to NM_018060.3 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr10:89717608 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr10:89717608 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr11:70118337 A>G maps to NM_003626.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr11:70118337 A>G maps to NM_003626.2 G20G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr12:113314456 G>C maps to NM_001143854.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr12:113314456 G>C maps to NM_001143854.1 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr14:105405142 C>A maps to NM_138420.2 E5549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr14:105405142 C>A maps to NM_138420.2 E5549*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr15:27017879 C>T maps to NM_021912.4 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr15:27017879 C>T maps to NM_021912.4 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr16:28986867 C>T maps to NM_032038.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr16:28986867 C>T maps to NM_032038.2 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr16:72828797 G>A maps to NM_006885.3 Q2595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr16:72828797 G>A maps to NM_006885.3 Q2595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr17:3806870 G>A maps to NM_002558.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr17:3806870 G>A maps to NM_002558.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr17:7477964 C>A maps to NM_001416.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr17:7477964 C>A maps to NM_001416.2 I58I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr17:16001721 G>A maps to ENST00000395857 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr17:16001721 G>A maps to ENST00000395857 L943L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr17:56276425 C>A maps to NM_000502.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr17:56276425 C>A maps to NM_000502.4 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr18:44561019 G>A maps to NM_016427.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr18:44561019 G>A maps to NM_016427.2 L206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:7676635 C>T maps to NM_001080429.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:7676635 C>T maps to NM_001080429.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:14991726 T>A maps to NM_030901.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:14991726 T>A maps to NM_030901.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:18967004 C>T maps to ENST00000418384 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:18967004 C>T maps to ENST00000418384 L585L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:39234769 G>A maps to NM_144691.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:39234769 G>A maps to NM_144691.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:46663961 C>T maps to NM_001002915.2 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr19:46663961 C>T maps to NM_001002915.2 D66D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:46739841 C>G maps to NM_080653.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:46739841 C>G maps to NM_080653.3 L3L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:136566628 G>A maps to NM_002299.2 A1096A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:136566628 G>A maps to NM_002299.2 A1096A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:179394997 C>T maps to NM_133378.4 R32880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:179394997 C>T maps to NM_133378.4 R32880R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:183826936 G>A maps to NM_205842.1 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:183826936 G>A maps to NM_205842.1 R617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:215823080 G>A maps to NM_173076.2 Q2013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:215823080 G>A maps to NM_173076.2 Q2013*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:241622113 G>A maps to NM_001102467.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr2:241622113 G>A maps to NM_001102467.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:34205118 G>C maps to NM_003116.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:34205118 G>C maps to NM_003116.1 L122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:35207245 G>A maps to NM_021809.6 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:35207245 G>A maps to NM_021809.6 G23G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:35207332 G>A maps to NM_021809.6 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:35207332 G>A maps to NM_021809.6 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:56098961 C>T maps to ENST00000423479 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr20:56098961 C>T maps to ENST00000423479 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr21:35183397 G>T maps to NM_003024.2 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr21:35183397 G>T maps to NM_003024.2 V813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr21:47786939 G>A maps to NM_006031.5 E1017E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr21:47786939 G>A maps to NM_006031.5 E1017E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr22:18609337 C>G maps to NM_018943.2 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr22:18609337 C>G maps to NM_018943.2 S198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr22:29456462 G>A maps to NM_015370.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr22:29456462 G>A maps to NM_015370.1 F124F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr3:47045570 C>T maps to NM_015175.1 I1962I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr3:47045570 C>T maps to NM_015175.1 I1962I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr4:146791580 C>T maps to ENST00000508784 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr4:146791580 C>T maps to ENST00000508784 E599E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr5:137589023 G>C maps to NM_001496.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr5:137589023 G>C maps to NM_001496.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr6:27775462 G>T maps to NM_003519.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr6:27775462 G>T maps to NM_003519.3 I74I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr6:30520379 A>C maps to NM_005275.3 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr6:30520379 A>C maps to NM_005275.3 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr6:127611067 C>T maps to NM_001139510.1 W290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr6:127611067 C>T maps to NM_001139510.1 W290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr7:80292451 C>T maps to NM_001127444.1 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr7:80292451 C>T maps to NM_001127444.1 Y192Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr9:131351131 C>G maps to NM_001130438.2 V972V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chr9:131351131 C>G maps to NM_001130438.2 V972V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chrX:3229027 G>A maps to NM_015419.3 Q2406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chrX:3229027 G>A maps to NM_015419.3 Q2406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chrX:63412989 G>C maps to NM_152424.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chrX:63412989 G>C maps to NM_152424.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chrX:90691094 C>T maps to NM_080832.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chrX:90691094 C>T maps to NM_080832.2 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chrX:112058754 G>C maps to NM_001113490.1 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23K-01A-11D-A16O-08 chrX:112058754 G>C maps to NM_001113490.1 S408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:9783272 C>G maps to ENST00000361110 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:9783272 C>G maps to ENST00000361110 L863L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:27272630 C>T maps to NM_006600.2 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:27272630 C>T maps to NM_006600.2 Q319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:44363934 C>T maps to NM_174963.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:44363934 C>T maps to NM_174963.2 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:109490304 A>G maps to NM_001048210.1 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:109490304 A>G maps to NM_001048210.1 Y89Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:161139703 G>T maps to NM_001122764.1 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:161139703 G>T maps to NM_001122764.1 E293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:214557892 G>A maps to NM_005401.4 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:214557892 G>A maps to NM_005401.4 I435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr10:72541759 G>T maps to NM_152710.2 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr10:72541759 G>T maps to NM_152710.2 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr10:85965625 C>T maps to NM_033100.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr10:85965625 C>T maps to NM_033100.2 I302I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr11:31477933 C>G did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr11:31477933 C>G did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr11:55872566 G>T maps to NM_001005200.1 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr11:55872566 G>T maps to NM_001005200.1 G17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr11:64563776 G>A maps to NM_004579.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr11:64563776 G>A maps to NM_004579.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr11:66287092 C>T maps to NM_024649.4 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr11:66287092 C>T maps to NM_024649.4 V199V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:6494465 C>T maps to NM_002342.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:6494465 C>T maps to NM_002342.1 F131F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:12815010 G>C maps to NM_006143.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:12815010 G>C maps to NM_006143.2 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:48578078 G>C maps to NM_001013635.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:48578078 G>C maps to NM_001013635.3 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:49428023 C>T maps to NM_003482.3 Q3522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:49428023 C>T maps to NM_003482.3 Q3522Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:59284454 G>C maps to NM_153377.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:59284454 G>C maps to NM_153377.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:70070806 C>G maps to NM_032735.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr12:70070806 C>G maps to NM_032735.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr13:101777026 G>A maps to NM_052867.2 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr13:101777026 G>A maps to NM_052867.2 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr14:24787689 G>A maps to NM_139247.3 Q1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr14:24787689 G>A maps to NM_139247.3 Q1056*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr14:73425479 C>T maps to NM_015604.3 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr14:73425479 C>T maps to NM_015604.3 V485V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr14:77919687 G>A maps to ENST00000445370 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr14:77919687 G>A maps to ENST00000445370 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr14:105418844 C>T maps to NM_138420.2 E981E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr14:105418844 C>T maps to NM_138420.2 E981E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr15:24923173 C>G maps to NM_018958.2 Y720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr15:24923173 C>G maps to NM_018958.2 Y720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr15:26866675 A>G maps to NM_021912.4 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr15:26866675 A>G maps to NM_021912.4 Y82Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr16:12136829 C>T maps to NM_032167.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr16:12136829 C>T maps to NM_032167.2 I108I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr16:23117736 G>C maps to NM_020718.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr16:23117736 G>C maps to NM_020718.3 L281L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr17:7487224 G>C maps to NM_004870.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr17:7487224 G>C maps to NM_004870.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr17:12898356 G>A maps to NM_018127.6 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr17:12898356 G>A maps to NM_018127.6 Q611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr17:73654525 C>T maps to NM_004259.5 W334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr17:73654525 C>T maps to NM_004259.5 W334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr19:45422485 G>C maps to NM_001645.3 *84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr19:45422485 G>C maps to NM_001645.3 *84S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr19:52149137 G>T maps to NM_001098612.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr19:52149137 G>T maps to NM_001098612.1 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:139308478 G>A maps to NM_001001664.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:139308478 G>A maps to NM_001001664.2 L69L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:197004444 G>A maps to NM_004226.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:197004444 G>A maps to NM_004226.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:201435771 G>C did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:201435771 G>C did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:230723834 G>C maps to ENST00000389044 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr2:230723834 G>C maps to ENST00000389044 S227*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr20:4163400 C>T maps to ENST00000443211 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr20:4163400 C>T maps to ENST00000443211 S425S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr22:40759014 C>T maps to NM_000026.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr22:40759014 C>T maps to NM_000026.2 T347T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr22:50655514 G>A maps to NM_031454.1 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr22:50655514 G>A maps to NM_031454.1 A601A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:38316944 C>G maps to NM_004256.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:38316944 C>G maps to NM_004256.3 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:123983407 C>T maps to NM_001024660.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:123983407 C>T maps to NM_001024660.3 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:172058909 G>A maps to NM_022763.3 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:172058909 G>A maps to NM_022763.3 Q620Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:179525525 G>A maps to NM_016559.1 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:179525525 G>A maps to NM_016559.1 Q538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:189585725 C>A maps to NM_003722.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr3:189585725 C>A maps to NM_003722.4 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr4:71201721 C>T maps to NM_033122.3 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr4:71201721 C>T maps to NM_033122.3 D322D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr4:77051822 G>A maps to ENST00000458189 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr4:77051822 G>A maps to ENST00000458189 Q349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr4:128886249 G>C maps to NM_152778.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr4:128886249 G>C maps to NM_152778.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:41039654 T>C maps to ENST00000296803 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:41039654 T>C maps to ENST00000296803 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:41176631 C>T maps to NM_001115131.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:41176631 C>T maps to NM_001115131.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:140516602 C>T maps to NM_015669.2 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:140516602 C>T maps to NM_015669.2 R529R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:153755918 G>A maps to NM_198321.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:153755918 G>A maps to NM_198321.3 L217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:167645659 C>A maps to NM_001122679.1 P1579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:167645659 C>A maps to NM_001122679.1 P1579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr6:30671973 A>G maps to NM_014641.2 P1662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr6:30671973 A>G maps to NM_014641.2 P1662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr6:73787561 T>C maps to NM_001160133.1 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr6:73787561 T>C maps to NM_001160133.1 D290D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr7:44555411 G>A maps to NM_013389.2 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr7:44555411 G>A maps to NM_013389.2 L1289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr7:149557787 G>A maps to NM_001099220.1 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr7:149557787 G>A maps to NM_001099220.1 V513V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr8:20107233 C>T maps to NM_021020.2 *597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr8:20107233 C>T maps to NM_021020.2 *597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr9:711530 G>A maps to NM_015158.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr9:711530 G>A maps to NM_015158.2 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr9:6534788 C>G did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr9:6534788 C>G did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chrX:51076023 G>A maps to NM_153183.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chrX:51076023 G>A maps to NM_153183.2 E69E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chrX:102333516 G>T maps to NM_022052.1 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chrX:102333516 G>T maps to NM_022052.1 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chrX:111078297 A>G maps to NM_012471.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chrX:111078297 A>G maps to NM_012471.2 L583L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr12:41582514 C>T maps to NM_001164595.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A0TN-01A-21D-A14W-08 chr12:41582514 C>T maps to NM_001164595.1 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chrX:151896141 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1BK-01B-11D-A13W-08 chrX:151896141 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr8:26238479 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MJ-01A-11D-A14W-08 chr8:26238479 C>T did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:27100987 C>T maps to NM_006015.4 Q1424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr1:27100987 C>T maps to NM_006015.4 Q1424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:76183419 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr17:76183419 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr18:18586467 G>A maps to NM_005406.2 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr18:18586467 G>A maps to NM_005406.2 Q577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr8:17944401 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MK-01A-11D-A14W-08 chr8:17944401 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr12:49434414 G>A maps to NM_003482.3 Q2380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr12:49434414 G>A maps to NM_003482.3 Q2380*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:55669029 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1ML-01A-11D-A14W-08 chr19:55669029 G>A did not map to a codon.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr15:99192758 T>C did not map to a codon.
Sequencing variant TCGA-C5-A1MP-01A-11D-A14W-08 chr15:99192758 T>C did not map to a codon.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27278877 G>T maps to NM_021831.5 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-C5-A1MQ-01A-11D-A14W-08 chr2:27278877 G>T maps to NM_021831.5 E413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr2:219128368 C>A maps to NM_170699.2 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZL-01A-11D-A10S-08 chr2:219128368 C>A maps to NM_170699.2 R308R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:16261838 C>G maps to NM_015001.2 S3035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:16261838 C>G maps to NM_015001.2 S3035*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:43886617 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr1:43886617 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:101643850 G>C maps to ENST00000342239 S1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr10:101643850 G>C maps to ENST00000342239 S1329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:56995490 C>A maps to NM_013449.3 E1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr12:56995490 C>A maps to NM_013449.3 E1306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:24684922 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr14:24684922 C>G did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:4836333 C>G maps to NM_000173.5 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr17:4836333 C>G maps to NM_000173.5 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:920504 G>A maps to NM_032551.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:920504 G>A maps to NM_032551.4 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:12800030 C>T maps to ENST00000380339 *489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr19:12800030 C>T maps to ENST00000380339 *489*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:113147113 G>A maps to NM_005054.2 F1136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr2:113147113 G>A maps to NM_005054.2 F1136F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:189026425 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr4:189026425 C>T did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:140579306 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr5:140579306 G>A did not map to a codon.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:151919141 G>C maps to ENST00000355193 S1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr7:151919141 G>C maps to ENST00000355193 S1148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:37556023 G>T maps to NM_025069.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DR-A0ZM-01A-12D-A10S-08 chr8:37556023 G>T maps to NM_025069.1 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:155023408 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr1:155023408 C>G did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr13:42830422 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr13:42830422 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr13:42830662 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr13:42830662 C>T did not map to a codon.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr18:20573290 C>T maps to ENST00000360790 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VM-01A-11D-A10S-08 chr18:20573290 C>T maps to ENST00000360790 Q501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr7:64452418 G>C maps to NM_001007253.3 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A0VN-01A-21D-A10S-08 chr7:64452418 G>C maps to NM_001007253.3 S329*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:6790189 A>C did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr11:6790189 A>C did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:72363551 A>G did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr17:72363551 A>G did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27776334 A>G maps to NM_003509.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:27776334 A>G maps to NM_003509.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:168227166 A>C did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chr6:168227166 A>C did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151896332 C>T did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151896332 C>T did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151896345 C>G did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151896345 C>G did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151896588 C>A did not map to a codon.
Sequencing variant TCGA-DS-A1OC-01A-11D-A14W-08 chrX:151896588 C>A did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:36358892 G>C maps to ENST00000312412 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr17:36358892 G>C maps to ENST00000312412 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27776334 A>G maps to NM_003509.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:27776334 A>G maps to NM_003509.2 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:168227166 A>C did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr6:168227166 A>C did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr9:36304139 C>T did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chr9:36304139 C>T did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151896219 G>A did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151896219 G>A did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151896248 A>C did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151896248 A>C did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151896345 C>G did not map to a codon.
Sequencing variant TCGA-DS-A1OD-01A-11D-A14W-08 chrX:151896345 C>G did not map to a codon.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:148346704 G>A maps to ENST00000369202 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EX-A1H5-01A-31D-A13W-08 chr1:148346704 G>A maps to ENST00000369202 L18L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:148344704 C>G maps to ENST00000369202 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr1:148344704 C>G maps to ENST00000369202 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr20:36932550 G>C did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr20:36932550 G>C did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:140529801 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr5:140529801 G>A did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr7:77325638 C>T did not map to a codon.
Sequencing variant TCGA-FU-A23L-01A-11D-A16O-08 chr7:77325638 C>T did not map to a codon.
