Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr19:57967674 G>A maps to NM_020633.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr19:579409 C>T did not map to a codon.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr7:48016401 G>T maps to NM_004507.2 T130T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr7:40899975 G>A maps to NM_001193311.1 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr12:9013728 A>G did not map to a codon.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr4:48591853 A>G maps to NM_015030.1 D516D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr1:238045748 C>T maps to NM_021186.3 K532K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr21:43547304 G>A maps to NM_173568.3 P1289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr10:103735058 T>C did not map to a codon.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr10:122273472 C>T maps to NM_001030059.1 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr19:9064375 C>T maps to NM_024690.2 P7690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr13:31728715 T>C did not map to a codon.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr11:74800584 G>T maps to NM_001005285.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0YZ-01A-11D-A10S-08 chr2:95773944 G>A maps to NM_031902.3 G204G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z0-01A-11D-A10S-08 chr19:40366100 T>C maps to NM_003890.2 A4711A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z0-01A-11D-A10S-08 chr8:133894134 T>C maps to NM_003235.4 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z0-01A-11D-A10S-08 chr10:89692931 T>A maps to NM_000314.4 L139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z0-01A-11D-A10S-08 chr16:69279565 G>A maps to NM_006750.3 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z0-01A-11D-A10S-08 chr4:110454842 T>A did not map to a codon.
Sequencing variant TCGA-BJ-A0Z0-01A-11D-A10S-08 chr1:35579877 T>A maps to NM_024772.3 L816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z2-01A-11D-A10S-08 chr18:14542920 G>A maps to ENST00000444806 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z2-01A-11D-A10S-08 chr17:47375972 C>A maps to NM_014897.2 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z2-01A-11D-A10S-08 chr9:35906343 G>A maps to NM_001039792.1 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z2-01A-11D-A10S-08 chr11:17144296 A>G maps to NM_002645.2 P821P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z2-01A-11D-A10S-08 chr7:141420815 A>T maps to NM_001105558.1 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z2-01A-11D-A10S-08 chr2:70121124 C>T maps to NM_006857.1 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z3-01A-11D-A13W-08 chr13:113742642 G>A maps to NM_001112732.1 A954A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z3-01A-11D-A13W-08 chr19:6682002 C>T maps to NM_000064.2 E1433E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z3-01A-11D-A13W-08 chr5:35800128 G>A maps to NM_024867.3 Q1630Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z9-01A-11D-A10S-08 chr2:21230693 C>A maps to NM_000384.2 E3016*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z9-01A-11D-A10S-08 chr19:50455610 G>A maps to NM_052884.2 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z9-01A-11D-A10S-08 chr8:22476664 G>T maps to NM_021174.5 E842*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z9-01A-11D-A10S-08 chrX:153593300 G>A maps to NM_001110556.1 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z9-01A-11D-A10S-08 chr7:149463283 G>A maps to NM_207336.1 Q103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z9-01A-11D-A10S-08 chr17:465846 T>C maps to NM_001128159.2 Q484Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0Z9-01A-11D-A10S-08 chr1:101198097 C>A maps to NM_001078.3 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZA-01A-11D-A10S-08 chr6:112462654 G>A maps to NM_001105206.1 Y906Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZA-01A-11D-A10S-08 chr18:32677459 T>C maps to NM_014268.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZA-01A-11D-A10S-08 chr18:28662245 T>C maps to ENST00000438199 V420V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZA-01A-11D-A10S-08 chr7:104786952 A>T maps to ENST00000336613 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr1:94639988 C>T maps to NM_004815.3 Q1074Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr15:66842424 G>C maps to NM_207338.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr2:179408636 G>A maps to NM_133378.4 Y29510Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr4:94693646 T>C maps to NM_001510.2 *1008R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr12:42836500 C>T maps to NM_016488.6 H361H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr1:222717147 G>A maps to NM_024746.3 A235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr15:85189403 T>C maps to ENST00000419751 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr3:142268515 C>G did not map to a codon.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr3:49899479 C>T maps to NM_024046.3 K75K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr8:48772220 G>C maps to NM_006904.6 S2052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr4:154533506 T>C maps to NM_001131007.1 S1174S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr10:50824647 T>G maps to NM_020549.4 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chrX:11200232 G>A maps to NM_013427.2 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr17:7330440 C>T maps to NM_175734.4 D377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZB-01A-11D-A10S-08 chr6:30681829 G>A maps to NM_014641.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZC-01A-12D-A13W-08 chr5:32774824 T>C maps to ENST00000265074 F357F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZC-01A-12D-A13W-08 chr14:31553972 A>T did not map to a codon.
Sequencing variant TCGA-BJ-A0ZC-01A-12D-A13W-08 chr1:110050829 G>A maps to NM_020703.2 H235H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZC-01A-12D-A13W-08 chr6:27841024 A>T maps to NM_003546.2 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZC-01A-12D-A13W-08 chr20:39831620 T>G maps to NM_015035.3 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZC-01A-12D-A13W-08 chr11:45959839 G>A maps to ENST00000257821 C492C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZC-01A-12D-A13W-08 chr8:30361915 G>A maps to NM_001008712.1 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZC-01A-12D-A13W-08 chr5:141364441 C>G maps to NM_183399.1 L437L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZC-01A-12D-A13W-08 chr6:1313343 G>T maps to NM_033260.3 S135S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZC-01A-12D-A13W-08 chr14:70477483 G>A maps to NM_001034852.1 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZE-01A-11D-A10S-08 chr4:170913278 G>A maps to NM_021647.6 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZE-01A-11D-A10S-08 chr2:167055181 C>G maps to ENST00000303354 *1990Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZE-01A-11D-A10S-08 chr11:82959005 C>T maps to ENST00000260047 G712G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZE-01A-11D-A10S-08 chr6:32917463 G>A maps to NM_006120.3 F192F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZE-01A-11D-A10S-08 chr12:49890688 A>G maps to NM_023071.3 Q200Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZE-01A-11D-A10S-08 chr2:189853338 C>A maps to NM_000090.3 P202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZE-01A-11D-A10S-08 chrX:74332768 A>G maps to NM_004299.3 C96C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZG-01A-11D-A10S-08 chr16:53243395 T>C maps to ENST00000219084 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZG-01A-11D-A10S-08 chr14:61442343 A>C maps to NM_020810.2 V431V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZG-01A-11D-A10S-08 chr21:31802979 C>A maps to NM_181600.1 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZH-01A-11D-A10S-08 chr16:57695713 C>T maps to NM_005682.5 I596I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZH-01A-11D-A10S-08 chr19:7914209 C>A maps to NM_001159944.1 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZH-01A-11D-A10S-08 chr7:139757773 A>G maps to NM_022750.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZH-01A-11D-A10S-08 chr19:9011325 G>C maps to NM_024690.2 V12969V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZH-01A-11D-A10S-08 chr12:109536205 C>G maps to NM_003362.3 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZH-01A-11D-A10S-08 chr20:49575531 G>A maps to NM_014484.3 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZH-01A-11D-A10S-08 chr17:48823270 C>A maps to ENST00000393227 S295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZH-01A-11D-A10S-08 chr19:36727353 C>T maps to NM_007145.2 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZH-01A-11D-A10S-08 chr17:1198816 C>T maps to NM_172367.2 D140D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZH-01A-11D-A10S-08 chr7:30491379 C>A maps to NM_006092.2 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A0ZJ-01A-11D-A10S-08 chr11:55135388 T>C maps to NM_001005275.1 F10F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A18Y-01A-11D-A13W-08 chr2:24245334 A>G maps to ENST00000338315 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A18Y-01A-11D-A13W-08 chr8:133899653 C>T maps to NM_003235.4 G679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A18Y-01A-11D-A13W-08 chr2:141259264 G>T maps to NM_018557.2 V2947V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A18Z-01A-21D-A13W-08 chr15:66207903 G>A maps to NM_032445.2 Q793*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A18Z-01A-21D-A13W-08 chr10:95556980 C>T maps to NM_005097.2 N365N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A191-01A-11D-A13W-08 chr9:116811045 C>T maps to ENST00000374126 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A191-01A-11D-A13W-08 chr16:56782201 C>T maps to NM_014669.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A191-01A-11D-A13W-08 chr17:32683580 C>G maps to NM_005408.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A191-01A-11D-A13W-08 chr13:45149844 G>C maps to NM_183422.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A191-01A-11D-A13W-08 chr19:3282182 G>C maps to NM_021938.3 V270V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A191-01A-11D-A13W-08 chr14:81744031 G>A maps to NM_033104.2 F541F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A191-01A-11D-A13W-08 chr18:56204583 G>C maps to NM_052947.3 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A191-01A-11D-A13W-08 chr14:59789678 C>T maps to NM_014992.1 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A191-01A-11D-A13W-08 chr17:15983373 G>A maps to ENST00000395857 T1151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A192-01A-31D-A13W-08 chr17:27182066 C>T maps to NM_005702.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A192-01A-31D-A13W-08 chr3:50230802 C>T maps to NM_000172.3 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A192-01A-31D-A13W-08 chr7:150554080 C>T maps to ENST00000416793 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28R-01A-11D-A16O-08 chr1:180651510 C>T maps to NM_004736.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28R-01A-11D-A16O-08 chr9:2718674 C>T maps to NM_133497.2 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28R-01A-11D-A16O-08 chr16:2260147 C>T maps to NM_182563.3 A105A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28R-01A-11D-A16O-08 chr16:84118641 G>C maps to NM_003791.2 S411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28S-01A-11D-A19J-08 chr11:6292022 C>T maps to NM_176875.2 G267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28S-01A-11D-A19J-08 chr19:45716590 G>A maps to NM_138568.3 L322L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28S-01A-11D-A19J-08 chrX:35989983 A>T did not map to a codon.
Sequencing variant TCGA-BJ-A28S-01A-11D-A19J-08 chr7:66262493 G>A did not map to a codon.
Sequencing variant TCGA-BJ-A28S-01A-11D-A19J-08 chr1:36381031 C>T maps to NM_012199.2 D639D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28S-01A-11D-A19J-08 chr11:61570927 G>A maps to NM_013402.4 F385F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28S-01A-11D-A19J-08 chr20:34242284 G>C maps to NM_001198838.1 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28V-01A-11D-A19J-08 chr17:64212936 C>A maps to NM_000042.2 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28V-01A-11D-A19J-08 chr19:5844723 C>A maps to NM_001097641.1 G43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28V-01A-11D-A19J-08 chr1:22084263 T>C maps to NM_032236.5 K49K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28V-01A-11D-A19J-08 chr3:124746058 G>A maps to NM_020733.1 D301D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28V-01A-11D-A19J-08 chr5:154393802 A>G maps to NM_001099293.1 K128K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28V-01A-11D-A19J-08 chr20:53267017 A>T maps to NM_018431.3 *307C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28V-01A-11D-A19J-08 chr12:14836052 G>A maps to NM_004963.3 N178N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28X-01A-11D-A22D-08 chr1:226050508 G>A maps to NM_014698.2 C263C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28X-01A-11D-A22D-08 chr11:58892673 G>A maps to NM_198947.3 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28X-01A-11D-A22D-08 chr1:52703745 G>A maps to NM_004799.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28X-01A-11D-A22D-08 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28X-01A-11D-A22D-08 chr5:140516095 G>A maps to NM_015669.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28X-01A-11D-A22D-08 chr14:105175024 C>T maps to ENST00000252520 A635A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28X-01A-11D-A22D-08 chr16:67473188 G>A maps to NM_004691.4 C209C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28X-01A-11D-A22D-08 chr3:108224617 T>C maps to NM_014981.1 K69K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28X-01A-11D-A22D-08 chr16:19883498 G>A maps to NM_016235.1 C223C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28X-01A-11D-A22D-08 chr14:24798361 G>A maps to NM_139247.3 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28Z-01A-11D-A16O-08 chr16:2358592 G>A maps to NM_001089.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28Z-01A-11D-A16O-08 chr3:182988118 G>A maps to NM_032047.4 W178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28Z-01A-11D-A16O-08 chr12:83289742 C>T maps to NM_152588.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28Z-01A-11D-A16O-08 chr17:12656260 G>A maps to NM_001146312.1 Q552Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28Z-01A-11D-A16O-08 chr7:90894812 C>A maps to NM_003505.1 G206G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28Z-01A-11D-A16O-08 chr10:43651085 C>T maps to NM_018590.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28Z-01A-11D-A16O-08 chr8:38005732 C>T maps to NM_000349.2 K97K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28Z-01A-11D-A16O-08 chr4:189060831 C>T maps to NM_178556.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28Z-01A-11D-A16O-08 chr6:117900211 G>A maps to NM_020399.3 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A28Z-01A-11D-A16O-08 chr16:10855243 G>C maps to NM_002484.2 R210R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr6:26156707 G>C maps to NM_005321.2 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr12:52913585 C>T maps to NM_000424.3 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr8:133880375 C>T maps to NM_003235.4 A28A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr20:62198472 C>T maps to NM_001037335.2 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr5:180622519 C>T maps to NM_203293.1 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr20:2594034 C>T maps to ENST00000424949 Q647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr16:20355365 G>A maps to ENST00000424589 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr6:15513523 C>T maps to NM_004973.2 S1107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr11:71293826 G>A maps to ENST00000376535 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr5:132158516 G>A maps to NM_001172700.1 Q844*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr12:1943778 C>T maps to NM_001163926.1 Y335Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr3:147128057 G>A maps to NM_003412.3 S53S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr11:124121060 C>A maps to ENST00000341493 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr15:86838595 G>C maps to NM_152336.2 T731T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr1:247769084 C>G maps to NM_001001914.1 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A290-01A-11D-A17V-08 chr1:1152972 G>T maps to NM_016176.3 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2N8-01A-11D-A18F-08 chrX:102632595 G>C maps to NM_206915.1 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2N8-01A-11D-A18F-08 chr10:43607565 C>A maps to NM_020975.4 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2N8-01A-11D-A18F-08 chrX:117815661 T>C maps to ENST00000276204 N1956N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2N8-01A-11D-A18F-08 chr1:196964998 G>T maps to ENST00000367414 G278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2N8-01A-11D-A18F-08 chrX:117053624 G>A maps to NM_033495.3 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2N8-01A-11D-A18F-08 chr7:88965205 A>G maps to NM_181646.2 S970S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2N9-01A-11D-A18F-08 chr12:6204448 G>T did not map to a codon.
Sequencing variant TCGA-BJ-A2N9-01A-11D-A18F-08 chr17:10402289 C>A did not map to a codon.
Sequencing variant TCGA-BJ-A2N9-01A-11D-A18F-08 chr9:8499763 G>A maps to NM_002839.3 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2N9-01A-11D-A18F-08 chr1:176054930 T>C maps to NM_022457.5 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2N9-01A-11D-A18F-08 chr22:30890947 G>A maps to NM_174977.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2N9-01A-11D-A18F-08 chr21:47783835 C>T maps to NM_006031.5 L866L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2N9-01A-11D-A18F-08 chr20:39984583 T>C maps to NM_022896.1 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr13:37622067 G>A maps to NM_001014286.2 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr1:35915474 C>T maps to NM_024874.4 V782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr19:49651467 C>T maps to NM_003660.2 N988N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr17:7139846 G>C maps to NM_024297.2 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr12:22487067 A>G maps to NM_003034.3 S33S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr12:81112652 T>C maps to NM_005593.2 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr6:90400466 C>T maps to NM_014611.1 R3558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr2:42991136 G>A maps to NM_148962.4 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chrX:100547853 G>A maps to NM_024885.3 D60D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr8:101661543 G>A maps to NM_152628.3 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr19:17313021 G>A maps to NM_004145.3 Q1582Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr6:150464573 G>T maps to NM_030949.2 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr11:57995528 C>T maps to NM_001004471.2 E273E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr6:24409747 C>T maps to NM_020662.2 Q121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chrX:152937597 G>A maps to NM_001039582.3 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2NA-01A-12D-A19J-08 chr6:157803238 C>T maps to NM_024630.2 G62G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2P4-01A-11D-A18F-08 chr10:46999057 C>T maps to NM_014696.3 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2P4-01A-11D-A18F-08 chr20:47845342 C>T maps to NM_017895.7 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2P4-01A-11D-A18F-08 chr11:128642761 C>T maps to NM_002017.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2P4-01A-11D-A18F-08 chr19:36303116 C>T maps to NM_021232.1 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2P4-01A-11D-A18F-08 chr20:61444703 G>A maps to NM_007346.2 S579S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2P4-01A-11D-A18F-08 chr16:70569223 A>T maps to NM_012426.4 S242S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A2P4-01A-11D-A18F-08 chr9:108510353 C>T maps to NM_018112.1 Y181Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3EZ-01A-11D-A202-08 chr1:179090741 C>T maps to NM_007314.3 V316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3EZ-01A-11D-A202-08 chr9:100919654 G>A did not map to a codon.
Sequencing variant TCGA-BJ-A3EZ-01A-11D-A202-08 chr4:175897116 T>C maps to NM_014269.4 H147H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3EZ-01A-11D-A202-08 chr1:14075950 G>C maps to NM_012231.4 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3EZ-01A-11D-A202-08 chr17:8218799 C>T maps to NM_173728.3 F443F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3EZ-01A-11D-A202-08 chr17:41585705 G>A did not map to a codon.
Sequencing variant TCGA-BJ-A3EZ-01A-11D-A202-08 chr7:150490265 G>C maps to NM_014020.3 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3EZ-01A-11D-A202-08 chr13:48611887 G>A maps to NM_018283.1 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3EZ-01A-11D-A202-08 chr8:38264954 G>T maps to ENST00000379957 G463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3EZ-01A-11D-A202-08 chr7:1542822 G>A maps to ENST00000389470 H149H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3F0-01A-11D-A202-08 chr14:93172866 C>A maps to NM_005606.6 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3F0-01A-11D-A202-08 chr16:67214354 G>A maps to NM_001040715.1 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3F0-01A-11D-A202-08 chr17:7481487 A>G maps to NM_001416.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3F0-01A-11D-A202-08 chr2:101564728 C>T maps to NM_002518.3 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3F0-01A-11D-A202-08 chr5:34826487 C>T maps to NM_001145521.1 L901L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PR-01A-11D-A21Z-08 chr10:28970194 C>T maps to NM_012342.2 R29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PR-01A-11D-A21Z-08 chr4:159750277 A>G maps to ENST00000379346 G117G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PR-01A-11D-A21Z-08 chr7:27237981 T>C maps to NM_000522.4 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PR-01A-11D-A21Z-08 chr4:111398001 C>T maps to NM_001977.3 L144L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PR-01A-11D-A21Z-08 chr6:53139894 G>A maps to ENST00000370918 C190C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PR-01A-11D-A21Z-08 chr15:62305291 G>A maps to NM_020821.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PT-01A-12D-A21Z-08 chr22:29091786 G>C maps to NM_001005735.1 Y433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PT-01A-12D-A21Z-08 chr19:49488754 G>A maps to NM_002103.4 T262T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PT-01A-12D-A21Z-08 chr6:20402609 C>T maps to NM_001949.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PT-01A-12D-A21Z-08 chr16:67211929 G>A maps to NM_001040715.1 L412L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PT-01A-12D-A21Z-08 chrX:152936611 G>A maps to NM_001039582.3 S299S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PT-01A-12D-A21Z-08 chr11:122680512 G>A maps to NM_032873.4 Q623Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PU-01A-11D-A21Z-08 chr8:2040222 G>A maps to NM_003970.2 T626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PU-01A-11D-A21Z-08 chr9:137323831 C>T maps to NM_002957.4 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PU-01A-11D-A21Z-08 chr19:34263439 C>T maps to NM_022467.3 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PU-01A-11D-A21Z-08 chr9:131355260 G>A did not map to a codon.
Sequencing variant TCGA-BJ-A3PU-01A-11D-A21Z-08 chr12:70732320 A>G maps to NM_014515.5 K333K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PU-01A-11D-A21Z-08 chr2:166536025 C>T maps to ENST00000409420 S539S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A3PU-01A-11D-A21Z-08 chr19:49536438 A>T maps to NM_033378.1 R151R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45D-01A-11D-A23U-08 chr17:74039960 T>C maps to NM_014230.2 K491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45E-01A-11D-A23U-08 chr12:53586180 C>T maps to NM_000889.1 Q696Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45F-01A-12D-A23U-08 chr19:15132291 C>T maps to NM_173482.2 A334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45G-01A-11D-A23U-08 chr14:21270002 C>T maps to NM_198235.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45G-01A-11D-A23U-08 chr4:146560392 C>T maps to NM_172250.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45G-01A-11D-A23U-08 chr19:13220603 T>C maps to NM_001136035.2 E385E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45I-01A-11D-A23U-08 chr5:179192841 G>A maps to NM_014757.4 E277E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45I-01A-11D-A23U-08 chr10:104309837 C>T maps to NM_016169.3 G143G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45I-01A-11D-A23U-08 chr1:90049453 G>A maps to NM_015350.2 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45I-01A-11D-A23U-08 chr4:114163299 A>C maps to NM_001148.4 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45J-01A-11D-A23U-08 chr19:1987242 G>A maps to NM_017797.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45J-01A-11D-A23U-08 chr15:75042336 G>A maps to NM_000761.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45J-01A-11D-A23U-08 chr2:45801776 G>A maps to NM_018079.4 F386F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45J-01A-11D-A23U-08 chr11:3687762 G>A maps to NM_020402.2 V309V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45J-01A-11D-A23U-08 chr11:56344738 G>A maps to NM_001004741.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45J-01A-11D-A23U-08 chr2:61438932 G>A maps to NM_014709.3 G2938G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45K-01A-11D-A23U-08 chr22:50755724 C>T maps to NM_001001794.3 Q150Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A45K-01A-11D-A23U-08 chr2:166866282 C>T maps to NM_001165963.1 R1316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A4O9-01A-11D-A257-08 chrX:31089692 G>A maps to NM_031894.2 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A4O9-01A-11D-A257-08 chr12:72956809 C>T maps to NM_013381.2 Q633*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A4O9-01A-11D-A257-08 chr12:55759421 C>T maps to NM_001005497.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A4O9-01A-11D-A257-08 chr19:16268600 G>A maps to NM_032855.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A4O9-01A-11D-A257-08 chr9:110074018 G>T did not map to a codon.
Sequencing variant TCGA-BJ-A4O9-01A-11D-A257-08 chr14:73491206 G>A maps to NM_021260.2 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A4O9-01A-11D-A257-08 chr15:75182419 C>T maps to NM_002435.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BJ-A4O9-01A-11D-A257-08 chr15:55497814 C>A maps to NM_183235.1 E186*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A13K-01A-11D-A10S-08 chr19:8389407 G>A maps to NM_198471.2 I769I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A13K-01A-11D-A10S-08 chr8:97251724 C>T maps to NM_015942.3 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A13K-01A-11D-A10S-08 chr7:93519447 C>A did not map to a codon.
Sequencing variant TCGA-CE-A13K-01A-11D-A10S-08 chr4:189068315 C>T maps to NM_178556.3 H399H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A13K-01A-11D-A10S-08 chr5:140724388 G>A maps to NM_018916.3 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A13K-01A-11D-A10S-08 chr6:44197516 C>T maps to ENST00000313248 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A27D-01A-11D-A16O-08 chr5:34811916 G>A maps to NM_001145521.1 V201V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3MD-01A-11D-A20C-08 chr1:39847745 G>A maps to ENST00000361689 E2528E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3MD-01A-11D-A20C-08 chr12:1225196 G>T maps to NM_178040.2 E523*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3MD-01A-11D-A20C-08 chr15:69331267 C>A maps to NM_024505.3 I481I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3ME-01A-11D-A20C-08 chr7:23792451 G>A did not map to a codon.
Sequencing variant TCGA-CE-A3ME-01A-11D-A20C-08 chr19:12962966 G>A maps to NM_014975.2 A305A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3ME-01A-11D-A20C-08 chr15:93007534 T>C maps to NM_006011.3 L350L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3ME-01A-11D-A20C-08 chr17:37563978 T>A maps to NM_004774.3 K1499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3ME-01A-11D-A20C-08 chr15:65459052 C>T maps to NM_006660.3 K143K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3ME-01A-11D-A20C-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3ME-01A-11D-A20C-08 chr11:14520417 T>C maps to NM_001144061.1 E19E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3ME-01A-11D-A20C-08 chr19:49589799 G>A maps to NM_003089.4 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3ME-01A-11D-A20C-08 chrX:153129443 G>A maps to NM_000425.3 F1117F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3ME-01A-11D-A20C-08 chr4:96761699 C>T maps to NM_005390.4 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A3ME-01A-11D-A20C-08 chr9:101829273 A>G maps to NM_001855.3 L1254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A482-01A-11D-A23U-08 chr16:31092930 C>T maps to NM_014699.3 T1762T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A482-01A-11D-A23U-08 chr10:115540476 G>A maps to NM_001193435.1 L346L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A482-01A-11D-A23U-08 chr10:375465 G>T maps to NM_014974.2 A1220A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A482-01A-11D-A23U-08 chr4:22517164 G>A maps to NM_145290.2 N81N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A482-01A-11D-A23U-08 chr3:12645670 G>A maps to ENST00000415519 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A484-01A-11D-A23U-08 chr1:97771736 C>T maps to NM_000110.3 K725K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A484-01A-11D-A23U-08 chr6:31323334 G>A maps to ENST00000428231 I288I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-CE-A484-01A-11D-A23U-08 chrX:26212472 C>T maps to NM_173523.2 A170A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0XZ-01A-11D-A17V-08 chr1:167095888 G>A maps to NM_001080426.1 R507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0XZ-01A-11D-A17V-08 chr4:100504661 A>C maps to ENST00000511045 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0XZ-01A-11D-A17V-08 chr17:74003918 T>C maps to NM_001988.2 S1789S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0XZ-01A-11D-A17V-08 chr18:76754114 G>A maps to NM_171999.2 K708K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0XZ-01A-11D-A17V-08 chrX:2407560 G>A maps to NM_004729.3 L400L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0XZ-01A-11D-A17V-08 chr1:248263051 C>T maps to NM_175911.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr18:33606927 G>A maps to NM_018170.3 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr13:95248339 C>T maps to NM_014305.2 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr10:5948519 C>T maps to NM_032807.3 F277F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr14:77778366 C>T maps to NM_013382.5 E86E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr10:64967026 G>A maps to NM_032776.1 Q1468*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr9:74971942 G>A maps to ENST00000437241 Q185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr15:26107934 C>T maps to NM_024490.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr8:57026478 C>T maps to NM_005372.1 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr2:97405603 C>T maps to NM_001142292.1 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr18:9950520 C>T maps to NM_003574.5 Q228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr1:92200372 T>C maps to NM_003243.4 E176E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y2-01A-11D-A10S-08 chr3:185929648 C>A maps to NM_001346.2 E618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y3-01B-11D-A10S-08 chr3:48508559 C>G maps to NM_016381.3 S224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y3-01B-11D-A10S-08 chr5:1443102 G>C maps to NM_001044.4 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y3-01B-11D-A10S-08 chr5:95748057 C>T maps to NM_000439.4 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y3-01B-11D-A10S-08 chr19:48254335 G>A maps to NM_015710.4 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y3-01B-11D-A10S-08 chr5:131008165 T>C maps to NM_133372.2 E657E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y3-01B-11D-A10S-08 chr14:70924857 T>A maps to NM_003813.2 V214V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y3-01B-11D-A10S-08 chr14:76012816 C>T maps to NM_006399.3 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y3-01B-11D-A10S-08 chr10:96066242 C>T maps to ENST00000371380 V1894V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A0Y3-01B-11D-A10S-08 chr5:138643133 C>T maps to ENST00000394800 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A2OL-01A-11D-A18F-08 chr12:2983215 T>G maps to NM_202002.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A2OL-01A-11D-A18F-08 chr1:13942397 A>G did not map to a codon.
Sequencing variant TCGA-DE-A3KN-01A-11D-A20C-08 chr6:24358037 C>T maps to NM_181337.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A3KN-01A-11D-A20C-08 chr17:43197709 G>A maps to NM_133373.3 Y222Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A4M8-01A-21D-A257-08 chr5:141329141 T>C maps to NM_016580.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A4M8-01A-21D-A257-08 chr3:12183430 G>A maps to NM_133625.3 V153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A4M8-01A-21D-A257-08 chr5:1280290 C>T maps to NM_198253.2 T644T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A4M8-01A-21D-A257-08 chr11:33777499 C>T maps to NM_012175.3 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A4M9-01A-11D-A257-08 chr3:169644877 C>T maps to NM_182610.2 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A4M9-01A-11D-A257-08 chr22:38251571 C>T maps to ENST00000262832 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DE-A4M9-01A-11D-A257-08 chr2:54081131 C>T maps to NM_006794.2 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13L-01A-11D-A21Z-08 chr19:54418664 C>T maps to NM_031896.4 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13L-01A-11D-A21Z-08 chr9:131709561 A>G maps to NM_014908.3 S7S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13L-01A-11D-A21Z-08 chr20:6068513 G>A maps to NM_017671.4 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13L-01A-11D-A21Z-08 chr12:133220460 G>A maps to ENST00000455752 L1421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13L-01A-11D-A21Z-08 chr17:78362949 C>A did not map to a codon.
Sequencing variant TCGA-DJ-A13L-01A-11D-A21Z-08 chr3:183882939 G>A maps to NM_004423.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13L-01A-11D-A21Z-08 chr7:23775293 A>T maps to NM_031414.3 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13L-01A-11D-A21Z-08 chr12:115120662 G>A maps to NM_016569.3 Q115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13L-01A-11D-A21Z-08 chr6:43173159 C>T maps to ENST00000354495 Q1598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13L-01A-11D-A21Z-08 chr15:44120431 A>G maps to NM_024908.3 Q110Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13M-01A-11D-A10S-08 chr2:236957788 C>A maps to NM_001037131.1 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13M-01A-11D-A10S-08 chr19:36558891 G>T maps to NM_001083961.1 E288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13M-01A-11D-A10S-08 chr4:165118488 G>A maps to NM_012403.1 N125N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13P-01A-11D-A10S-08 chrX:22112114 T>G maps to NM_000444.4 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13P-01A-11D-A10S-08 chr9:75775258 A>G maps to NM_000700.1 Q117Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13P-01A-11D-A10S-08 chr12:54348805 G>T maps to NM_173860.1 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13P-01A-11D-A10S-08 chr11:35232955 T>C maps to NM_000610.3 T590T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13P-01A-11D-A10S-08 chrX:13778526 A>T maps to NM_003611.2 R650*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13R-01A-11D-A10S-08 chr9:139733835 G>A maps to NM_001173988.1 S553S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13R-01A-11D-A10S-08 chr4:170628368 C>T maps to NM_173872.2 Q701*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13R-01A-11D-A10S-08 chr12:44172021 C>T maps to NM_016123.3 H286H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13R-01A-11D-A10S-08 chr3:164741468 T>A maps to NM_001041.3 T996T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13R-01A-11D-A10S-08 chr5:154395056 C>T maps to NM_001099293.1 N546N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13R-01A-11D-A10S-08 chr20:47611020 C>T maps to NM_006420.2 Q1003*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13R-01A-11D-A10S-08 chr2:101592001 C>T maps to NM_002518.3 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13R-01A-11D-A10S-08 chr1:36181502 G>A maps to NM_152374.1 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13S-01A-11D-A10S-08 chr1:180010892 G>T maps to NM_014810.4 E1440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13S-01A-11D-A10S-08 chr5:138643172 G>A maps to ENST00000394800 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13S-01A-11D-A10S-08 chr2:168105212 G>A maps to NM_152381.5 K2437K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13T-01A-11D-A10S-08 chrX:26212808 G>A maps to NM_173523.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13T-01A-11D-A10S-08 chr13:84453857 G>A maps to NM_052910.1 N595N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13U-01A-11D-A10S-08 chr10:1042090 C>A maps to NM_012341.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13U-01A-11D-A10S-08 chr1:27949581 C>T maps to NM_005248.2 K100K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13U-01A-11D-A10S-08 chr3:44670565 A>G did not map to a codon.
Sequencing variant TCGA-DJ-A13U-01A-11D-A10S-08 chr21:22804491 C>A maps to NM_004540.2 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13U-01A-11D-A10S-08 chr9:117071595 G>A maps to NM_032888.2 E1758E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13U-01A-11D-A10S-08 chr7:142563826 C>T maps to NM_004445.3 V405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13U-01A-11D-A10S-08 chr4:178359916 G>A maps to NM_000027.3 C163C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13V-01A-11D-A10S-08 chr19:8987281 C>T maps to NM_024690.2 L13935L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13V-01A-11D-A10S-08 chr9:134019853 G>A maps to ENST00000451030 T494T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13V-01A-11D-A10S-08 chr3:182937643 C>T maps to NM_015078.2 K790K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13V-01A-11D-A10S-08 chr21:16338128 T>C maps to NM_003489.3 L795L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13W-01A-11D-A10S-08 chr3:100567711 C>T maps to ENST00000471714 Q510Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13W-01A-11D-A10S-08 chr12:72388216 A>G did not map to a codon.
Sequencing variant TCGA-DJ-A13W-01A-11D-A10S-08 chr1:109492525 T>C maps to NM_001048210.1 S49S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13W-01A-11D-A10S-08 chr17:71375611 C>T maps to NM_001144952.1 P1613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13W-01A-11D-A10S-08 chr1:156038144 G>A maps to NM_020387.2 K108K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A13X-01A-11D-A10S-08 chr7:2740234 G>A maps to NM_133463.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QE-01A-21D-A14W-08 chr8:48625363 T>C maps to NM_001080394.1 S706S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QE-01A-21D-A14W-08 chr3:52454957 A>G maps to ENST00000454052 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QE-01A-21D-A14W-08 chr8:118817026 A>G maps to NM_000127.2 A663A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QE-01A-21D-A14W-08 chrX:2864075 C>A maps to NM_000047.2 L318L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QF-01A-12D-A14W-08 chr16:81157273 G>A maps to NM_052892.3 L2155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QF-01A-12D-A14W-08 chr16:18860686 T>C maps to ENST00000389467 Q1825Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QF-01A-12D-A14W-08 chr10:91144285 T>C maps to NM_001010987.2 L406L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QF-01A-12D-A14W-08 chr1:215792547 T>C maps to NM_016121.3 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QF-01A-12D-A14W-08 chr7:104782686 T>C maps to ENST00000336613 T468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QF-01A-12D-A14W-08 chr1:178834452 T>C maps to NM_004673.3 Q153Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QF-01A-12D-A14W-08 chr18:33271055 G>A maps to NM_020474.3 T353T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QF-01A-12D-A14W-08 chr17:80579583 G>A maps to NM_019613.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QF-01A-12D-A14W-08 chr5:141307807 C>A maps to NM_014773.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QF-01A-12D-A14W-08 chr19:9074482 A>G maps to NM_024690.2 A4321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QG-01A-11D-A14W-08 chr11:60274283 C>G maps to NM_017716.2 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QG-01A-11D-A14W-08 chr9:108483838 G>A maps to NM_018112.1 P97P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QG-01A-11D-A14W-08 chr17:42090385 G>T maps to NM_032376.2 L152L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QG-01A-11D-A14W-08 chr1:152328851 C>T maps to NM_001014342.2 G470G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QG-01A-11D-A14W-08 chr19:10449574 C>T maps to NM_002162.3 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QG-01A-11D-A14W-08 chr1:42925431 T>C maps to NM_024664.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QG-01A-11D-A14W-08 chr1:169811623 C>T maps to NM_018186.2 Q598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QG-01A-11D-A14W-08 chr1:247875915 A>G maps to NM_001005286.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QH-01A-21D-A14W-08 chr21:19770629 C>T maps to NM_002772.2 Q54Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QH-01A-21D-A14W-08 chr11:88911585 C>A maps to NM_000372.4 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QH-01A-21D-A14W-08 chr17:53063606 A>G maps to NM_178509.5 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QH-01A-21D-A14W-08 chr9:119460293 C>T maps to NM_012210.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QH-01A-21D-A14W-08 chrX:102977176 A>G maps to NM_001024452.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QH-01A-21D-A14W-08 chr15:42115280 C>T maps to NM_001128608.1 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QI-01A-11D-A14W-08 chr10:50902593 T>C maps to NM_001042427.1 G76G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DJ-A1QI-01A-11D-A14W-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DJ-A1QI-01A-11D-A14W-08 chr13:100807309 C>G maps to NM_000282.3 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QI-01A-11D-A14W-08 chr15:49776582 G>A maps to NM_002009.3 W156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QI-01A-11D-A14W-08 chr1:79116041 T>A maps to NM_006417.4 I54I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QL-01A-11D-A14W-08 chr2:178098701 A>G did not map to a codon.
Sequencing variant TCGA-DJ-A1QL-01A-11D-A14W-08 chr20:43836651 C>T maps to NM_003007.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QL-01A-11D-A14W-08 chr11:113705032 G>A maps to NM_020886.2 R187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QL-01A-11D-A14W-08 chr11:64326626 C>T maps to NM_018484.2 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QL-01A-11D-A14W-08 chr4:113508690 C>T maps to NM_018392.4 E1174E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QL-01A-11D-A14W-08 chr5:140857071 C>T maps to NM_002588.2 D463D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QM-01A-11D-A14W-08 chr3:57543395 G>A maps to NM_177966.5 Q430Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QM-01A-11D-A14W-08 chrX:16720908 G>A maps to NM_001144002.1 I39I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QM-01A-11D-A14W-08 chr11:117090318 G>A maps to NM_004716.2 F437F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QM-01A-11D-A14W-08 chr5:167182183 G>A did not map to a codon.
Sequencing variant TCGA-DJ-A1QM-01A-11D-A14W-08 chr8:135649755 C>T maps to NM_020863.3 R132R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QN-01A-11D-A14W-08 chr17:74006560 G>A maps to NM_001988.2 Q909*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QN-01A-11D-A14W-08 chr2:27357184 G>A maps to NM_013388.4 G35G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QO-01A-11D-A14W-08 chr2:85276642 C>T maps to NM_020122.4 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QO-01A-11D-A14W-08 chr4:366798 A>G maps to NM_003441.2 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QO-01A-11D-A14W-08 chr11:6261927 C>T maps to NM_001037329.2 R302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QO-01A-11D-A14W-08 chr6:157521925 C>T maps to ENST00000367148 Q1440*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QO-01A-11D-A14W-08 chr11:20404723 G>A maps to NM_001098520.1 G268G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QO-01A-11D-A14W-08 chr10:98087289 C>T maps to NM_004088.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QO-01A-11D-A14W-08 chr13:77673089 C>T maps to NM_015057.4 E2733E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QQ-01A-11D-A14W-08 chr19:9236921 A>G maps to NM_001001958.1 Y235Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QQ-01A-11D-A14W-08 chr8:144940614 G>A maps to NM_031308.1 T2269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QQ-01A-11D-A14W-08 chr13:37596274 G>A maps to ENST00000475892 Q591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QQ-01A-11D-A14W-08 chr3:38651438 C>T maps to NM_001099404.1 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QQ-01A-11D-A14W-08 chr17:37333710 A>G maps to NM_000723.3 Y408Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A1QQ-01A-11D-A14W-08 chr16:81232603 G>A maps to NM_052892.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PN-01A-21D-A19J-08 chr8:94935009 G>A maps to NM_001161778.1 K300K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PN-01A-21D-A19J-08 chr19:47935697 G>A maps to NM_015063.2 D705D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PN-01A-21D-A19J-08 chr4:186545307 C>G maps to ENST00000355634 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PN-01A-21D-A19J-08 chr7:780547 C>T maps to NM_017802.3 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PO-01A-21D-A19J-08 chr15:44085951 A>T maps to ENST00000409960 R99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PO-01A-21D-A19J-08 chr11:73879564 C>T maps to ENST00000334126 W50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PO-01A-21D-A19J-08 chr7:140374544 G>C maps to NM_052853.3 L356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PP-01A-11D-A19J-08 chr7:16649338 G>A maps to NM_020319.2 I266I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PP-01A-11D-A19J-08 chr2:51254682 G>A maps to ENST00000404971 C243C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PP-01A-11D-A19J-08 chr1:235920718 T>C maps to NM_000081.2 L2307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PP-01A-11D-A19J-08 chr17:34185529 C>T did not map to a codon.
Sequencing variant TCGA-DJ-A2PP-01A-11D-A19J-08 chr1:153315683 G>A maps to NM_020393.2 N118N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PP-01A-11D-A19J-08 chr7:92869234 G>A maps to NM_017667.2 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PP-01A-11D-A19J-08 chr5:37169006 T>C maps to NM_023073.3 P2373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PQ-01A-11D-A18F-08 chr7:138579147 G>A maps to NM_001164665.1 C1324C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PQ-01A-11D-A18F-08 chr17:73908311 G>A maps to ENST00000389570 L1094L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PQ-01A-11D-A18F-08 chr2:27599353 T>C maps to NM_014748.2 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PQ-01A-11D-A18F-08 chr19:15052785 C>A maps to NM_012377.1 T162T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PR-01A-11D-A19J-08 chr1:52251508 C>G maps to ENST00000428468 S620*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PR-01A-11D-A19J-08 chr3:9976165 G>A maps to NM_001077415.2 W15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PR-01A-11D-A19J-08 chr19:50720897 C>T maps to NM_001145809.1 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PS-01A-11D-A18F-08 chr10:12215789 G>A maps to ENST00000378937 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PS-01A-11D-A18F-08 chr11:865529 G>A maps to ENST00000409531 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PT-01A-11D-A18F-08 chr20:5923211 C>T maps to NM_015939.3 Q296Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PT-01A-11D-A18F-08 chr6:13307946 C>A maps to NM_016495.4 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PT-01A-11D-A18F-08 chr5:140237798 G>A maps to NM_018901.2 S722S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PT-01A-11D-A18F-08 chr10:135202534 A>G maps to NM_152911.2 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PU-01A-12D-A19J-08 chrX:153001963 C>T maps to NM_000033.3 R464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PU-01A-12D-A19J-08 chrX:133700184 G>T maps to NM_021796.3 V176V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PV-01A-11D-A19J-08 chr1:236719121 G>A maps to NM_018072.5 R1878*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PV-01A-11D-A19J-08 chr19:40745947 T>C did not map to a codon.
Sequencing variant TCGA-DJ-A2PV-01A-11D-A19J-08 chr12:120897755 C>T maps to NM_176818.2 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PV-01A-11D-A19J-08 chr20:20582428 C>T maps to NM_020343.3 R700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PV-01A-11D-A19J-08 chr5:50091187 C>G maps to ENST00000505697 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PW-01A-11D-A19J-08 chr22:40719205 A>T maps to ENST00000454349 L1835L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PW-01A-11D-A19J-08 chr1:46032686 C>G maps to NM_153326.1 A117A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PW-01A-11D-A19J-08 chr19:49713616 C>T maps to NM_017636.3 R1095*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PW-01A-11D-A19J-08 chr3:3887995 G>A maps to NM_020873.5 S557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PW-01A-11D-A19J-08 chr1:38465012 G>A maps to NM_004468.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PW-01A-11D-A19J-08 chr7:151859890 G>A maps to ENST00000355193 Q3591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PY-01A-11D-A18F-08 chr4:79517009 G>A maps to NM_005139.2 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PY-01A-11D-A18F-08 chr6:134495196 C>T maps to NM_001143676.1 L153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PY-01A-11D-A18F-08 chr9:130672243 G>A maps to NM_175039.3 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PY-01A-11D-A18F-08 chr2:157352614 T>G maps to NM_000408.4 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PY-01A-11D-A18F-08 chrX:100911290 T>C maps to NM_177949.2 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PY-01A-11D-A18F-08 chr1:9804007 G>A maps to NM_001009566.1 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PY-01A-11D-A18F-08 chr10:15655756 C>A maps to NM_003638.1 P485P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PZ-01A-21D-A18F-08 chr19:36637182 C>A maps to NM_001749.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PZ-01A-21D-A18F-08 chr9:132397703 C>G maps to NM_014064.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PZ-01A-21D-A18F-08 chr1:155838392 C>T maps to NM_152280.4 D224D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2PZ-01A-21D-A18F-08 chr6:34985385 C>T maps to NM_015245.2 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chr1:248845497 C>T maps to NM_001004734.1 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chr3:52485803 C>G maps to NM_003280.2 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chr5:147051353 G>A maps to NM_014790.3 R6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chr17:72926755 C>A maps to NM_178160.2 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chr1:6291979 G>T maps to NM_012405.3 Y218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chr10:99968513 G>T maps to ENST00000314594 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chr15:44581274 C>T maps to NM_138423.3 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chr16:71768592 G>C maps to ENST00000423132 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chr6:52129523 G>A maps to ENST00000419835 I808I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chrX:12885600 T>G did not map to a codon.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chr8:131848584 C>A maps to NM_001115.2 L871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q0-01A-11D-A202-08 chr20:29960790 C>T maps to NM_054112.2 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q1-01A-22D-A19J-08 chr7:95442506 G>A did not map to a codon.
Sequencing variant TCGA-DJ-A2Q1-01A-22D-A19J-08 chr3:142278215 A>G maps to NM_001184.3 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q1-01A-22D-A19J-08 chr2:230664035 G>T maps to ENST00000389044 Y1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q2-01A-11D-A19J-08 chr19:43382239 G>A maps to NM_006905.2 D85D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q2-01A-11D-A19J-08 chr2:25470534 C>T maps to NM_175629.1 W313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q2-01A-11D-A19J-08 chr17:40836232 C>T maps to NM_003632.2 R117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q2-01A-11D-A19J-08 chr5:11098686 C>T maps to NM_001332.2 K879K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q2-01A-11D-A19J-08 chr14:56139948 A>G maps to NM_001079521.1 V1249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q2-01A-11D-A19J-08 chr2:119915191 G>A maps to NM_182528.3 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q3-01A-11D-A18F-08 chr2:179419248 G>A maps to NM_133378.4 R27041*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q3-01A-11D-A18F-08 chr7:63720696 A>G maps to NM_153363.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q3-01A-11D-A18F-08 chr2:242680472 A>G maps to NM_152783.3 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q3-01A-11D-A18F-08 chr19:5111517 C>G maps to ENST00000381759 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q3-01A-11D-A18F-08 chr12:6659950 G>A maps to NM_001193457.1 A280A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q4-01A-21D-A18F-08 chr5:24537753 T>A maps to NM_006727.3 G87G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q4-01A-21D-A18F-08 chr16:56782201 C>T maps to NM_014669.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q4-01A-21D-A18F-08 chr1:152193153 C>G maps to NM_001009931.1 G317G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q6-01A-11D-A18F-08 chr11:7690410 G>A did not map to a codon.
Sequencing variant TCGA-DJ-A2Q6-01A-11D-A18F-08 chr17:36484930 T>C maps to ENST00000398597 K1508K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q6-01A-11D-A18F-08 chr3:64133073 C>T maps to NM_198859.3 R364R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q6-01A-11D-A18F-08 chr5:10414576 A>G maps to NM_005885.2 T643T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q6-01A-11D-A18F-08 chr10:11370889 T>C maps to NM_006561.3 G480G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q6-01A-11D-A18F-08 chr2:185802430 C>T maps to NM_194250.1 R770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q6-01A-11D-A18F-08 chr20:46313294 C>T maps to NM_001161841.1 P256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q6-01A-11D-A18F-08 chr9:97084600 G>A maps to NM_017561.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q7-01A-11D-A18F-08 chr19:6213133 G>A maps to NM_005934.3 T533T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q7-01A-11D-A18F-08 chr9:125681790 T>C maps to NM_020924.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q7-01A-11D-A18F-08 chr6:96651639 C>G maps to NM_006581.3 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q7-01A-11D-A18F-08 chr11:55927550 C>T maps to NM_001004058.2 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q7-01A-11D-A18F-08 chr5:88047812 G>C maps to NM_002397.4 S150S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q7-01A-11D-A18F-08 chr8:53092727 C>T maps to NM_014682.2 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q7-01A-11D-A18F-08 chr17:10295951 A>T maps to NM_002472.2 L1825L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q8-01A-11D-A18F-08 chr11:47369996 G>A maps to ENST00000399249 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q8-01A-11D-A18F-08 chr16:3828106 A>T maps to NM_004380.2 L673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q8-01A-11D-A18F-08 chr5:124079863 T>C maps to NM_020747.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q8-01A-11D-A18F-08 chr3:196675176 C>G maps to NM_025163.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q9-01A-21D-A18F-08 chr8:144940614 G>A maps to NM_031308.1 T2269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q9-01A-21D-A18F-08 chrX:74293734 G>T maps to NM_004299.3 Y305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q9-01A-21D-A18F-08 chr11:68181158 C>T maps to NM_002335.2 Q836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q9-01A-21D-A18F-08 chr9:104071535 C>T maps to NM_017753.2 N143N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2Q9-01A-21D-A18F-08 chr2:220162110 C>G maps to NM_002846.3 R644R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2QA-01A-11D-A18F-08 chr1:159683395 G>A maps to NM_000567.2 F198F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2QA-01A-11D-A18F-08 chr5:5463853 G>A maps to NM_015325.1 K1469K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2QA-01A-11D-A18F-08 chr2:121050796 G>A maps to NM_002881.2 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2QA-01A-11D-A18F-08 chr17:56283863 G>A maps to NM_017777.3 G484G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2QB-01A-11D-A19J-08 chr5:140568535 G>C maps to NM_019119.3 A548A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2QB-01A-11D-A19J-08 chr1:205128808 T>G did not map to a codon.
Sequencing variant TCGA-DJ-A2QC-01A-11D-A18F-08 chr10:102267769 C>T maps to NM_015490.3 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2QC-01A-11D-A18F-08 chr16:89352007 G>C maps to NM_013275.4 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2QC-01A-11D-A18F-08 chr8:25340934 T>G maps to ENST00000434814 Y352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2QC-01A-11D-A18F-08 chr7:100454532 C>T maps to NM_020246.2 Y164Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2QC-01A-11D-A18F-08 chr1:212964937 G>A maps to NM_015471.3 F56F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A2QC-01A-11D-A18F-08 chr8:145948216 G>A maps to NM_138367.1 L276L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UK-01A-11D-A22D-08 chr17:77926571 G>A maps to NM_019020.2 N275N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UK-01A-11D-A22D-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UK-01A-11D-A22D-08 chrX:49113413 G>A maps to ENST00000455775 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UK-01A-11D-A22D-08 chr6:13283733 C>T maps to NM_030948.1 D530D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UK-01A-11D-A22D-08 chr4:16900066 G>A maps to NM_001290.3 F14F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UK-01A-11D-A22D-08 chr4:80246701 G>A maps to NM_032693.2 H110H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UK-01A-11D-A22D-08 chr17:18232138 C>T maps to NM_004169.3 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UK-01A-11D-A22D-08 chr10:98188428 C>A maps to NM_012465.3 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UK-01A-11D-A22D-08 chr10:43869918 C>G maps to NM_173160.2 G13G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UK-01A-11D-A22D-08 chr20:853716 G>A maps to NM_015985.2 Y466Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UK-01A-11D-A22D-08 chr11:76751194 G>A maps to ENST00000354301 K200K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UM-01A-11D-A22D-08 chrX:73811994 G>A maps to NM_183353.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UM-01A-11D-A22D-08 chr19:56244557 G>A maps to NM_176820.2 I213I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UN-01A-11D-A22D-08 chr1:33985467 C>A maps to ENST00000373381 L3520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UN-01A-11D-A22D-08 chr17:27024967 C>T maps to NM_003170.3 T1456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UN-01A-11D-A22D-08 chr4:57976130 G>A maps to NM_001553.1 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UN-01A-11D-A22D-08 chr5:73931989 G>A maps to NM_003633.2 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UN-01A-11D-A22D-08 chr5:127654569 C>G did not map to a codon.
Sequencing variant TCGA-DJ-A3UN-01A-11D-A22D-08 chr7:19156403 C>A maps to NM_000474.3 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UN-01A-11D-A22D-08 chr3:45153737 G>A maps to NM_022842.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UN-01A-11D-A22D-08 chr11:94113643 G>A maps to NM_016540.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UN-01A-11D-A22D-08 chr1:175046793 G>A maps to NM_022093.1 E80E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UO-01A-11D-A22D-08 chr6:33272092 C>T maps to NM_172208.2 E397E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UO-01A-11D-A22D-08 chr17:6908625 G>T maps to NM_000697.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UO-01A-11D-A22D-08 chr1:204115852 G>A maps to NM_018208.2 H186H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UO-01A-11D-A22D-08 chr19:10789304 C>T maps to NM_017620.2 N192N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UO-01A-11D-A22D-08 chr6:147830171 C>A maps to NM_001030060.2 I36I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UP-01A-11D-A22D-08 chr3:133667434 G>A maps to NM_005630.2 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UP-01A-11D-A22D-08 chr19:8028429 G>A maps to ENST00000351593 N333N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UP-01A-11D-A22D-08 chr7:158935228 G>A maps to ENST00000402066 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UP-01A-11D-A22D-08 chr19:50180554 C>G maps to NM_001536.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UP-01A-11D-A22D-08 chr8:124033739 C>T did not map to a codon.
Sequencing variant TCGA-DJ-A3UP-01A-11D-A22D-08 chr2:160240181 G>A maps to NM_013450.2 D1232D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UQ-01A-11D-A22D-08 chr19:15514818 G>A did not map to a codon.
Sequencing variant TCGA-DJ-A3UQ-01A-11D-A22D-08 chr1:32498904 C>A maps to NM_006559.1 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UQ-01A-11D-A22D-08 chr19:52272348 C>T maps to NM_001005738.1 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UQ-01A-11D-A22D-08 chr1:244582070 C>T maps to NM_001126.3 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UQ-01A-11D-A22D-08 chr4:100532611 T>C did not map to a codon.
Sequencing variant TCGA-DJ-A3UR-01A-11D-A22D-08 chr17:18029722 G>A maps to ENST00000205890 P1273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UR-01A-11D-A22D-08 chr19:55525818 G>A maps to NM_001083899.1 C498C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UR-01A-11D-A22D-08 chr2:20205862 C>T maps to NM_002381.4 Q144Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UR-01A-11D-A22D-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UR-01A-11D-A22D-08 chr2:132235870 C>T maps to NM_080386.2 D46D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3US-01A-11D-A22D-08 chr2:122122644 A>C did not map to a codon.
Sequencing variant TCGA-DJ-A3US-01A-11D-A22D-08 chr20:2380226 A>T maps to NM_198994.2 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3US-01A-11D-A22D-08 chr6:96034276 G>A did not map to a codon.
Sequencing variant TCGA-DJ-A3US-01A-11D-A22D-08 chr22:22318658 C>A maps to NM_003935.3 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UT-01A-11D-A22D-08 chr16:19580876 A>C maps to NM_020314.5 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UT-01A-11D-A22D-08 chr1:152190915 G>T maps to NM_001009931.1 Y1063*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UT-01A-11D-A22D-08 chr5:176468157 C>T maps to ENST00000503039 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UT-01A-11D-A22D-08 chr11:46455149 G>A maps to ENST00000458649 S950S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UT-01A-11D-A22D-08 chrX:129546576 C>T maps to NM_016024.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UU-01A-11D-A22D-08 chr9:131019438 G>A maps to NM_004486.4 N972N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UU-01A-11D-A22D-08 chrX:19369469 C>T maps to NM_001173454.1 H159H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UU-01A-11D-A22D-08 chr6:152332841 G>A maps to NM_001122741.1 W383*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UW-01A-11D-A22D-08 chr11:117984148 A>G maps to NM_019894.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UW-01A-11D-A22D-08 chr15:45427464 G>A maps to NM_175940.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UW-01A-11D-A22D-08 chr19:18368262 G>A maps to NM_001145304.1 G1277G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UX-01A-11D-A22D-08 chr4:84465711 A>G maps to NM_032717.3 K55K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UX-01A-11D-A22D-08 chr8:144941253 G>A maps to NM_031308.1 D2056D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UX-01A-11D-A22D-08 chr17:25909678 G>A maps to ENST00000268763 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UX-01A-11D-A22D-08 chr15:89424648 G>A maps to NM_178232.2 Y144Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UX-01A-11D-A22D-08 chr20:40118564 A>G maps to NM_032221.3 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UX-01A-11D-A22D-08 chr4:146059040 A>G maps to ENST00000447906 H962H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UX-01A-11D-A22D-08 chr11:608071 G>A maps to ENST00000264555 T872T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3UX-01A-11D-A22D-08 chr1:155263297 G>A maps to ENST00000423816 D425D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3V7-01A-11D-A23M-08 chr3:58395860 G>A maps to NM_017771.3 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3V7-01A-11D-A23M-08 chr3:151127117 C>T maps to NM_053002.4 Q1935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3V7-01A-11D-A23M-08 chr11:68542875 G>A maps to NM_001876.3 Q495*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3V7-01A-11D-A23M-08 chr4:890298 T>C maps to NM_005255.2 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3V7-01A-11D-A23M-08 chrX:152225804 G>A maps to NM_013364.4 S131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VA-01A-11D-A23M-08 chr19:33666303 C>T maps to NM_173479.3 C415C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VA-01A-11D-A23M-08 chr8:97243453 T>C did not map to a codon.
Sequencing variant TCGA-DJ-A3VA-01A-11D-A23M-08 chr4:56428580 G>T maps to NM_152401.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VA-01A-11D-A23M-08 chr7:27856611 A>T maps to ENST00000409980 R704R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VA-01A-11D-A23M-08 chr5:71492991 C>T maps to NM_005909.3 T1270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VA-01A-11D-A23M-08 chr9:104356699 G>C maps to NM_147180.2 L171L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VB-01A-11D-A23M-08 chr13:114324126 C>T maps to NM_002929.2 I275I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VB-01A-11D-A23M-08 chr12:119916994 C>T maps to NM_178499.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VB-01A-11D-A23M-08 chrX:47918135 A>G maps to NM_001037735.2 H565H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VE-01A-11D-A23M-08 chr9:130374690 C>G maps to NM_003165.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VE-01A-11D-A23M-08 chr9:140777317 C>T maps to ENST00000277549 F171F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VE-01A-11D-A23M-08 chr10:73587776 G>A maps to ENST00000373120 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VE-01A-11D-A23M-08 chr6:75884985 C>T maps to ENST00000322507 T826T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VF-01A-11D-A23M-08 chr14:70634770 T>A maps to NM_183002.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VF-01A-11D-A23M-08 chr17:27209046 C>A did not map to a codon.
Sequencing variant TCGA-DJ-A3VF-01A-11D-A23M-08 chr22:19028787 G>A maps to NM_005137.2 G393G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VF-01A-11D-A23M-08 chr12:106633704 G>A maps to NM_006825.3 S302S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VJ-01A-11D-A23M-08 chr9:72082819 G>A maps to NM_001163.3 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VK-01A-11D-A23M-08 chr14:35742768 A>G maps to NM_014672.2 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VK-01A-11D-A23M-08 chr12:64587879 G>A maps to ENST00000311915 H360H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VK-01A-11D-A23M-08 chr22:30776279 G>A maps to NM_001017981.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VK-01A-11D-A23M-08 chr4:84377235 C>T maps to NM_016067.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VK-01A-11D-A23M-08 chr17:48431803 C>T maps to NM_022167.2 Q222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VL-01A-11D-A23M-08 chr19:16024589 C>T maps to NM_021187.3 E509E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VM-01A-11D-A23M-08 chr3:123345768 G>A maps to NM_053025.3 Q1712*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VM-01A-11D-A23M-08 chr8:133883767 G>T maps to NM_003235.4 G150G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VM-01A-11D-A23M-08 chr7:56079523 T>C maps to NM_004577.3 Q203Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VM-01A-11D-A23M-08 chr3:43345282 A>T maps to NM_017719.4 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VM-01A-11D-A23M-08 chr7:129906738 C>T maps to NM_001869.2 I6I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A3VM-01A-11D-A23M-08 chr19:10225801 C>T maps to NM_003755.3 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UL-01A-11D-A257-08 chr11:640584 C>T maps to NM_000797.3 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UL-01A-11D-A257-08 chr6:31496940 G>A maps to NM_001011700.2 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UL-01A-11D-A257-08 chr17:74011028 G>C maps to NM_001988.2 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UP-01A-11D-A257-08 chr22:20759721 G>A maps to NM_003426.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UP-01A-11D-A257-08 chr19:36245362 C>T maps to NM_019104.1 Y243Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr2:101009859 C>T maps to NM_004854.3 P306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr1:109560176 G>A maps to NM_001142550.1 Q69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chrX:153184647 G>A maps to NM_001164741.1 V297V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr11:65144370 C>A maps to NM_182556.2 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr1:176852035 G>A maps to ENST00000281881 I1115I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr2:105924338 G>A maps to NM_004257.4 I140I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr10:104140003 A>C did not map to a codon.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr6:28056395 T>C maps to NM_003447.3 I202I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr1:11907289 G>T maps to NM_006172.3 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr10:1070567 A>G maps to NM_033261.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr7:50129290 G>A maps to NM_007009.2 R48*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr17:67261046 C>G did not map to a codon.
Sequencing variant TCGA-DJ-A4UW-01A-11D-A257-08 chrX:100658837 A>C maps to NM_000169.2 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UW-01A-11D-A257-08 chr15:42114279 C>T maps to NM_001128608.1 C1007C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UW-01A-11D-A257-08 chrX:1428412 C>T maps to ENST00000432318 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UW-01A-11D-A257-08 chr6:116600260 G>A maps to NM_003309.3 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V0-01A-11D-A257-08 chr2:27728638 C>T maps to NM_001486.3 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V2-01A-11D-A257-08 chr3:42906479 G>T maps to NM_001296.4 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V2-01A-11D-A257-08 chr17:36486994 G>A maps to ENST00000398597 S820S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V2-01A-11D-A257-08 chr15:35045226 G>A maps to NM_020660.1 R140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V2-01A-11D-A257-08 chr5:26903744 C>T did not map to a codon.
Sequencing variant TCGA-DJ-A4V2-01A-11D-A257-08 chr3:142266706 G>A maps to NM_001184.3 Q1073*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V4-01A-11D-A257-08 chr10:104596872 G>T maps to NM_000102.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V4-01A-11D-A257-08 chr17:914041 G>C maps to NM_021962.2 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V4-01A-11D-A257-08 chr11:117314616 C>A maps to NM_020693.2 E1343*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V4-01A-11D-A257-08 chr7:157874038 C>T maps to NM_002847.3 V558V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V4-01A-11D-A257-08 chr15:43738723 C>T maps to NM_001141980.1 E967E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V4-01A-11D-A257-08 chr5:32274214 A>G maps to NM_001040446.1 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V4-01A-11D-A257-08 chr2:64780024 G>T maps to ENST00000422803 E473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V5-01A-11D-A257-08 chr19:3600479 G>A maps to NM_201636.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V5-01A-11D-A257-08 chr11:120169032 C>T maps to NM_014352.2 H64H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4V5-01A-11D-A257-08 chr16:56309932 C>T maps to NM_020988.2 I84I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A1K0-01A-11D-A13W-08 chrX:122616870 T>C maps to NM_000828.4 Y887Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A1K0-01A-11D-A13W-08 chr12:46125034 A>G maps to NM_152641.2 E74E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A1K0-01A-11D-A13W-08 chr11:60636684 G>A maps to NM_207341.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr15:75091136 G>A did not map to a codon.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr5:180048728 C>T maps to NM_182925.4 K611K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr12:46244996 C>T maps to NM_152641.2 Q1031*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr12:10862689 T>C maps to NM_003651.4 E199E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr16:69201032 C>G maps to NM_032830.2 S630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr17:2233811 C>T maps to NM_018128.4 Q589Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr11:7064627 C>G maps to NM_176822.3 V457V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr11:36597775 C>T maps to NM_000448.2 F974F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr19:47177806 C>T maps to ENST00000449438 G880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr6:42976210 C>T maps to NM_006245.2 Q342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr1:46080812 C>T maps to NM_002482.3 Q599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr5:173337560 G>A maps to NM_030627.2 E387E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr12:43858535 C>T did not map to a codon.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr11:125780317 G>A maps to NM_013264.3 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr4:71346813 C>G maps to NM_152291.2 S118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr11:125780285 T>C maps to NM_013264.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr19:3586870 C>T maps to NM_133261.2 I157I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr1:24078448 C>T maps to NM_003198.2 Q478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr6:31543616 C>T maps to NM_000594.2 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr13:99063013 C>T maps to NM_005766.2 F543F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr1:10209301 T>C maps to NM_001105562.2 Y884Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chrX:46898445 G>A maps to NM_001077445.1 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr13:45914211 G>A maps to ENST00000309246 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr1:156821795 G>A maps to NM_014215.2 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr17:42458005 G>A maps to NM_000419.3 I467I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr12:104851269 C>A maps to NM_018413.5 I27I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr16:48395649 A>G maps to NM_001006610.1 H261H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr12:54741786 G>A maps to NM_016057.1 V133V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr2:227662791 G>A maps to NM_005544.2 F221F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chrX:37027622 G>A maps to NM_001013736.2 P380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr11:65731498 C>T did not map to a codon.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr17:10533477 C>T maps to NM_002470.2 Q1831Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr10:97817701 C>T maps to NM_001134375.1 Q286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DO-A2HM-01B-11D-A22D-08 chr3:52238847 C>T maps to ENST00000441729 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3DY-01A-11D-A20C-08 chr9:140332515 C>A maps to NM_001033113.1 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3DY-01A-11D-A20C-08 chr2:70408979 T>A maps to NM_017880.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3DY-01A-11D-A20C-08 chr2:192234338 C>A maps to NM_001130158.1 I368I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3DZ-01A-11D-A20C-08 chr7:51092970 C>T maps to ENST00000395542 L1283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3DZ-01A-11D-A20C-08 chr12:72667127 G>A maps to NM_013381.2 E190E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3DZ-01A-11D-A20C-08 chr9:112705374 G>A maps to ENST00000413420 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3DZ-01A-11D-A20C-08 chr14:105242099 G>A maps to NM_001014432.1 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3DZ-01A-11D-A20C-08 chr6:39512313 C>G maps to ENST00000373213 V481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3DZ-01A-11D-A20C-08 chr10:43089113 G>A maps to NM_006955.1 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3DZ-01A-11D-A20C-08 chr5:176919615 G>A maps to NM_005451.3 I53I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E0-01A-11D-A20C-08 chr14:24774189 G>T maps to NM_174913.1 V600V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E0-01A-11D-A20C-08 chr8:37795174 G>A maps to NM_152413.2 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E0-01A-11D-A20C-08 chr7:50057889 T>C maps to NM_007009.2 K243K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E0-01A-11D-A20C-08 chrX:123556254 G>C maps to NM_001163278.1 L1446L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E0-01A-11D-A20C-08 chr1:155147748 G>A did not map to a codon.
Sequencing variant TCGA-E3-A3E0-01A-11D-A20C-08 chr3:124629311 G>T maps to NM_033049.3 I428I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E1-01A-11D-A20C-08 chr1:100366292 G>A maps to ENST00000311030 W1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E1-01A-11D-A20C-08 chr15:43489544 G>T maps to NM_000119.2 T707T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E1-01A-11D-A20C-08 chr2:159477860 G>A maps to NM_003628.3 Q177Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E1-01A-11D-A20C-08 chr1:38409492 G>C maps to ENST00000373026 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E1-01A-11D-A20C-08 chr2:73486157 C>T maps to ENST00000295133 R921R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E1-01A-11D-A20C-08 chr11:62414647 G>A maps to NM_030628.1 R968R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E1-01A-11D-A20C-08 chrX:149931174 C>T maps to NM_003828.2 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E1-01A-11D-A20C-08 chr5:176886213 G>A maps to ENST00000393565 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E2-01A-11D-A20C-08 chr6:88385611 T>C maps to NM_018064.3 Q189Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E2-01A-11D-A20C-08 chr15:92981585 G>A maps to NM_006011.3 K98K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E2-01A-11D-A20C-08 chr9:35396934 G>A did not map to a codon.
Sequencing variant TCGA-E3-A3E3-01A-11D-A20C-08 chr1:34037303 A>G maps to ENST00000373381 S2555S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E3-01A-11D-A20C-08 chrX:55650461 C>T maps to NM_198451.3 N106N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E5-01A-11D-A20C-08 chr2:37227777 T>C maps to NM_019024.1 T1832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E5-01A-11D-A20C-08 chr3:38420766 C>T maps to NM_005108.3 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E5-01A-11D-A20C-08 chr1:196883706 C>T maps to NM_006684.2 Y174Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E3-A3E5-01A-11D-A20C-08 chr11:8015970 A>T did not map to a codon.
Sequencing variant TCGA-E3-A3E5-01A-11D-A20C-08 chr18:14850290 T>C maps to NM_001145029.1 L1039L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A242-01A-21D-A16O-08 chr17:62496217 G>A maps to NM_004396.3 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A242-01A-21D-A16O-08 chr11:62546413 G>C maps to NM_006473.2 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A242-01A-21D-A16O-08 chrX:52825586 A>G maps to NM_001009616.2 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A242-01A-21D-A16O-08 chrX:150155678 G>C maps to NM_005342.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A242-01A-21D-A16O-08 chr11:130286919 G>A maps to NM_007037.4 I337I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A242-01A-21D-A16O-08 chr2:105859028 G>C maps to NM_007227.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A242-01A-21D-A16O-08 chr19:16496011 T>A maps to ENST00000455140 G725G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A2EA-01A-11D-A17V-08 chr19:56153900 C>G maps to NM_001163423.1 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A2EA-01A-11D-A17V-08 chr4:39910083 G>T maps to NM_001100399.1 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A2EA-01A-11D-A17V-08 chr13:39541132 G>A maps to NM_145286.2 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A2EA-01A-11D-A17V-08 chr7:100677147 G>C maps to NM_001040105.1 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A2EA-01A-11D-A17V-08 chr13:99339858 C>G maps to NM_005073.3 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A2EA-01A-11D-A17V-08 chr19:52376483 C>A maps to NM_032679.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A2EA-01A-11D-A17V-08 chr11:5686236 G>C maps to NM_033034.2 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A2EA-01A-11D-A17V-08 chr12:4708954 G>A did not map to a codon.
Sequencing variant TCGA-E8-A413-01A-21D-A23M-08 chr13:41949683 T>G maps to NM_024561.4 P847P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A413-01A-21D-A23M-08 chr13:46559771 A>G maps to ENST00000242848 D460D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A415-01A-11D-A23M-08 chr9:97062728 C>T maps to NM_194320.2 R297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A415-01A-11D-A23M-08 chr5:148624540 G>A maps to NM_014945.2 S483S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A418-01A-11D-A23M-08 chr19:49132444 T>C maps to NM_020126.3 A460A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A418-01A-11D-A23M-08 chr15:34649403 C>T maps to ENST00000438749 L1055L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A418-01A-11D-A23M-08 chr1:2334475 C>T maps to NM_007033.4 H168H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A418-01A-11D-A23M-08 chr1:17559435 C>T maps to NM_013358.2 G428G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A418-01A-11D-A23M-08 chr8:134232917 C>T maps to NM_003882.2 D148D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A419-01A-11D-A23M-08 chr19:44564908 A>G maps to NM_013361.4 Q50Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A419-01A-11D-A23M-08 chr9:91628469 G>T maps to NM_016848.5 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A433-01A-11D-A23M-08 chr2:9463375 C>T maps to NM_003887.2 C199C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A436-01A-12D-A23U-08 chr21:45819239 G>A maps to ENST00000397932 V708V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A436-01A-12D-A23U-08 chr16:70500882 C>T maps to ENST00000428974 C153C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A436-01A-12D-A23U-08 chr7:140155657 T>A maps to NM_013446.3 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A436-01A-12D-A23U-08 chr1:46867851 C>G maps to NM_001441.2 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A436-01A-12D-A23U-08 chr19:51022054 G>A maps to NM_001080457.1 R305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A436-01A-12D-A23U-08 chr1:68619273 G>A maps to NM_024911.6 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A437-01A-12D-A23U-08 chr12:41966815 C>T maps to NM_001164595.1 C745C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A437-01A-12D-A23U-08 chr2:201718130 A>G maps to NM_001162407.1 F493F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A437-01A-12D-A23U-08 chr10:98806445 G>A maps to NM_003061.2 S606S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A437-01A-12D-A23U-08 chr6:49754597 G>A maps to NM_138733.4 G101G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A44K-01A-21D-A23U-08 chr19:45998114 C>G maps to NM_005619.3 G76G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A44K-01A-21D-A23U-08 chr17:56557350 T>C maps to NM_001080439.1 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A44K-01A-21D-A23U-08 chr19:56153894 G>A maps to NM_001163423.1 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A44K-01A-21D-A23U-08 chr7:140394531 C>T maps to NM_052853.3 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-E8-A44M-01A-21D-A23U-08 chr7:150325516 C>A maps to ENST00000438845 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CL-01A-11D-A19J-08 chr21:41711100 G>A maps to NM_001389.3 C484C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CL-01A-11D-A19J-08 chr14:33291665 A>G maps to NM_004274.4 T1549T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CL-01A-11D-A19J-08 chr1:41979173 G>A maps to NM_024503.3 P1906P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CL-01A-11D-A19J-08 chr19:1037874 C>G maps to NM_004368.2 Y302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CM-01A-11D-A19J-08 chr3:9965965 C>T maps to NM_153461.2 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CM-01A-11D-A19J-08 chr9:99113431 G>A maps to NM_007001.2 I147I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CM-01A-11D-A19J-08 chr12:102314991 A>G did not map to a codon.
Sequencing variant TCGA-EL-A3CM-01A-11D-A19J-08 chr11:17432133 G>A maps to ENST00000302539 L876L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chr19:6702223 C>A did not map to a codon.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chr3:134873066 G>A maps to NM_004441.4 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chrX:154157201 G>A maps to NM_000132.3 N1621N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chr11:112040054 G>A did not map to a codon.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chr2:32312618 A>G maps to NM_014946.3 K158K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chr4:146059040 A>G maps to ENST00000447906 H962H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chr19:38959718 C>T maps to NM_000540.2 G1165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chr1:155028662 C>T maps to NM_207197.1 F284F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chr7:74212377 T>C maps to NM_173537.2 K491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chr14:20666078 G>A maps to NM_001005503.1 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chrX:108631735 G>T maps to ENST00000218006 R980R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CN-01A-12D-A20C-08 chr11:93103316 C>T maps to NM_181645.3 Q171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CO-01A-11D-A19J-08 chr16:61687934 G>A maps to NM_001796.2 D659D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CO-01A-11D-A19J-08 chr10:79011014 C>T did not map to a codon.
Sequencing variant TCGA-EL-A3CP-01A-11D-A19J-08 chr9:117166262 G>T maps to NM_015404.3 G777G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CP-01A-11D-A19J-08 chr5:176314336 C>T maps to NM_002115.2 E534E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CP-01A-11D-A19J-08 chr6:46656683 G>A maps to NM_001010870.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CR-01A-12D-A202-08 chr8:100832175 C>T maps to NM_017890.3 S2965S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CR-01A-12D-A202-08 chr11:6942666 C>T maps to NM_001004684.1 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CR-01A-12D-A202-08 chr6:27114963 T>G maps to NM_080596.1 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CR-01A-12D-A202-08 chr5:140181291 C>T maps to NM_018906.2 Y170Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CR-01A-12D-A202-08 chr8:143623677 G>A maps to NM_001702.2 E1361E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CR-01A-12D-A202-08 chr15:34355790 C>T maps to NM_012125.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CR-01A-12D-A202-08 chr2:25469563 G>A maps to NM_175629.1 Q402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CR-01A-12D-A202-08 chr1:4832583 C>T maps to NM_018836.3 R388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CR-01A-12D-A202-08 chr20:30602786 G>A maps to ENST00000300415 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CS-01A-21D-A19J-08 chr14:70924422 C>A maps to NM_003813.2 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CS-01A-21D-A19J-08 chr16:72090086 G>A maps to NM_005143.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CS-01A-21D-A19J-08 chr10:64973685 G>T maps to NM_032776.1 T747T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CS-01A-21D-A19J-08 chr12:40076925 C>T maps to NM_001031748.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr14:20586458 A>T maps to NM_001004715.1 V298V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr19:10381885 C>T maps to NM_000201.2 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr9:2718866 G>A maps to NM_133497.2 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr7:150753684 G>A maps to NM_004935.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr6:31133467 G>A maps to NM_002701.4 F179F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr5:167887656 G>A maps to NM_001161661.1 L942L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr19:2877813 G>A maps to NM_024967.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr11:66263136 G>A maps to NM_005700.3 V538V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr3:49169962 C>T maps to NM_002292.3 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr22:50752657 C>T maps to NM_001001794.3 L372L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr9:138516116 C>T maps to NM_182974.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr6:26225756 C>T maps to NM_003532.2 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr5:138651746 A>T did not map to a codon.
Multiple mappings detected for codon TCGA-EL-A3CT-01A-12D-A202-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr15:69561468 C>T maps to NM_015554.1 T580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr14:58863032 C>T maps to NM_207377.2 Q52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr12:89745585 G>A maps to NM_001946.2 F77F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr1:145584526 T>A maps to NM_006099.3 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr11:62299934 G>A maps to NM_001620.1 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr19:10395809 C>T maps to NM_000201.2 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr12:13224330 G>A did not map to a codon.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr10:61666112 G>A maps to ENST00000395341 Q24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr18:32438300 C>T maps to NM_001390.4 Q502*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr4:76861901 G>A maps to NM_014435.3 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr19:14736375 G>A maps to NM_032571.3 I616I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr7:50514708 G>A maps to NM_022116.3 Q93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr21:37507777 G>A maps to NM_001236.3 K96K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr18:31463211 G>A maps to NM_003787.4 S573S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr5:167553840 G>A maps to NM_001122679.1 A764A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr1:226036681 G>A maps to NM_014698.2 F701F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr5:140810403 C>T maps to NM_003735.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CT-01A-12D-A202-08 chr15:90611784 C>T maps to NM_198526.2 F472F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CU-01A-11D-A19J-08 chr4:959853 G>A maps to NM_001347.2 Q481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CU-01A-11D-A19J-08 chr10:103908242 C>T maps to NM_015062.3 S1505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CU-01A-11D-A19J-08 chr17:7761467 C>T maps to NM_144607.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CU-01A-11D-A19J-08 chr1:192150497 A>G maps to NM_130782.2 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CU-01A-11D-A19J-08 chr22:38318080 G>A maps to NM_033386.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CV-01A-11D-A19J-08 chr6:109787074 T>A maps to NM_014797.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CV-01A-11D-A19J-08 chr16:84438696 G>A maps to ENST00000420010 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CV-01A-11D-A19J-08 chr22:24109617 G>A maps to ENST00000401675 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CW-01A-11D-A19J-08 chr7:75959219 C>A maps to NM_012479.3 G140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CW-01A-11D-A19J-08 chr12:48091472 G>A maps to NM_024604.2 D108D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CW-01A-11D-A19J-08 chr19:16614021 C>T maps to NM_032207.2 H302H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CW-01A-11D-A19J-08 chr22:46643009 G>A maps to NM_207327.4 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CW-01A-11D-A19J-08 chr5:156533624 A>C did not map to a codon.
Sequencing variant TCGA-EL-A3CX-01A-11D-A19J-08 chr5:112116591 C>T maps to NM_001127510.2 R213*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CX-01A-11D-A19J-08 chr3:98073449 T>C maps to NM_001005517.1 F251F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CY-01A-11D-A19J-08 chr14:39560842 C>T maps to NM_006364.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CY-01A-11D-A19J-08 chr17:1400055 G>C maps to NM_016532.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3CZ-01A-11D-A19J-08 chr10:103292734 C>T maps to NM_033637.2 C335C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr5:140908071 G>C maps to ENST00000398557 P1032P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr13:72204796 A>G maps to ENST00000359684 A341A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr11:104825693 C>T maps to NM_001225.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr2:43902585 C>T maps to NM_001101330.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr15:64446697 G>A maps to NM_024798.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr6:43325105 G>A maps to NM_014345.2 R316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr10:22022989 T>C maps to NM_004641.3 P946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr16:31096482 C>A maps to NM_001039503.2 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr14:24538026 C>T maps to NM_138360.3 P1278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr20:44666023 G>A maps to NM_001134771.1 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr8:120650731 A>G maps to NM_006209.3 N23N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr21:45999780 G>A maps to NM_198694.2 C225C. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EL-A3D0-01A-12D-A202-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr2:175335222 C>T maps to NM_152529.5 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr19:50957537 G>A maps to NM_004533.3 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D0-01A-12D-A202-08 chr19:48244667 C>A maps to NM_014601.3 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D1-01A-11D-A19J-08 chr9:139914927 G>A maps to ENST00000355090 L459L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D4-01A-11D-A19J-08 chr17:7495765 G>A maps to ENST00000423172 V179V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D4-01A-11D-A19J-08 chr9:125288963 G>A maps to ENST00000359439 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D4-01A-11D-A19J-08 chr9:5812997 T>C maps to NM_024896.2 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D5-01A-22D-A202-08 chr4:164247094 C>T maps to NM_000909.4 S204S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D5-01A-22D-A202-08 chrX:53114504 T>A did not map to a codon.
Sequencing variant TCGA-EL-A3D5-01A-22D-A202-08 chr12:54367561 G>T maps to NM_014212.3 G179G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D5-01A-22D-A202-08 chr16:70599363 A>T maps to NM_012426.4 A921A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D5-01A-22D-A202-08 chr5:140531379 C>T maps to NM_018939.2 L514L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D5-01A-22D-A202-08 chr2:169850357 G>A maps to NM_003742.2 Q216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr16:48311246 A>T did not map to a codon.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr17:74015141 C>G did not map to a codon.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr10:131943567 A>G maps to NM_006541.4 Q62Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr19:14015678 G>A maps to ENST00000454313 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr9:100409797 C>T maps to NM_002486.4 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr3:175455162 T>C maps to NM_207015.2 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr3:27444775 C>G maps to ENST00000454389 V725V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr14:70522511 C>T did not map to a codon.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr14:94847271 G>A maps to NM_001127707.1 Q285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr17:7572985 G>A maps to NM_001126112.1 Q375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr11:2334909 C>T maps to NM_139022.2 Y127Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr10:64973912 T>A maps to NM_032776.1 R672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D6-01A-12D-A202-08 chr20:58558036 C>T maps to NM_177980.2 F151F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GO-01A-11D-A202-08 chr7:140481430 C>G maps to NM_004333.4 V459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GP-01A-11D-A202-08 chr20:36869356 T>C maps to NM_001029864.1 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GP-01A-11D-A202-08 chr3:107097051 C>T maps to NM_032600.2 D206D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GP-01A-11D-A202-08 chr17:5076149 T>A maps to NM_004505.2 Y1366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GP-01A-11D-A202-08 chr2:32477650 C>G maps to NM_021209.4 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GP-01A-11D-A202-08 chr7:149171561 G>A maps to NM_001163474.1 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GP-01A-11D-A202-08 chr1:248813366 A>T maps to NM_001001824.1 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GP-01A-11D-A202-08 chr12:117725988 G>T maps to ENST00000338101 S339S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GP-01A-11D-A202-08 chr20:31022740 G>C maps to ENST00000375687 G742G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GQ-01A-11D-A202-08 chr14:91770292 G>A maps to NM_001080414.2 S1129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GQ-01A-11D-A202-08 chrX:78426794 G>A maps to NM_032553.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GQ-01A-11D-A202-08 chr17:58034707 T>C maps to NM_016125.3 Q294Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GQ-01A-11D-A202-08 chr3:42597459 G>A maps to NM_032970.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GR-01A-21D-A202-08 chr1:158582605 C>T did not map to a codon.
Sequencing variant TCGA-EL-A3GR-01A-21D-A202-08 chr17:41577391 C>G maps to NM_004941.1 L489L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GR-01A-21D-A202-08 chr4:170641065 T>C maps to NM_173872.2 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GR-01A-21D-A202-08 chr11:105961347 A>G maps to NM_015423.2 E158E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GS-01A-11D-A20C-08 chr6:55739438 G>A maps to NM_021073.2 S75S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GS-01A-11D-A20C-08 chr3:99567861 A>G maps to NM_001042459.1 F886F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GS-01A-11D-A20C-08 chr7:106513028 G>A maps to NM_002649.2 L681L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GU-01A-11D-A21A-08 chr11:1977592 G>A maps to NM_021134.3 Q135Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GU-01A-11D-A21A-08 chr17:6553676 A>G maps to NM_016060.2 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GU-01A-11D-A21A-08 chr1:201779153 G>A maps to ENST00000367296 V1494V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GU-01A-11D-A21A-08 chr9:13125350 T>C maps to ENST00000319217 K1557K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GU-01A-11D-A21A-08 chr1:229568531 G>A maps to NM_001100.3 H75H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GU-01A-11D-A21A-08 chr9:137721850 C>T maps to NM_000093.3 N1699N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GU-01A-11D-A21A-08 chr1:44442970 C>T did not map to a codon.
Sequencing variant TCGA-EL-A3GU-01A-11D-A21A-08 chrX:54841925 T>C maps to NM_201222.1 S544S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GU-01A-11D-A21A-08 chr3:197746189 G>A maps to NM_001136049.2 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GU-01A-11D-A21A-08 chr7:131073682 A>T maps to NM_013255.4 K118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GV-01A-11D-A21A-08 chr15:45545718 G>C did not map to a codon.
Sequencing variant TCGA-EL-A3GV-01A-11D-A21A-08 chr3:170078418 G>T maps to NM_005414.3 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GV-01A-11D-A21A-08 chr8:144811135 C>T did not map to a codon.
Sequencing variant TCGA-EL-A3GV-01A-11D-A21A-08 chr8:21924654 T>G maps to ENST00000265800 S26S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GV-01A-11D-A21A-08 chr18:7231663 G>A maps to NM_001105581.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GV-01A-11D-A21A-08 chr6:167728843 G>A maps to NM_018974.3 G426G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GW-01A-11D-A202-08 chr9:35079473 C>T maps to NM_004629.1 W16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GW-01A-11D-A202-08 chr14:71051559 G>A maps to ENST00000430055 G244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GW-01A-11D-A202-08 chr7:150774838 G>C maps to NM_006712.3 R356R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GW-01A-11D-A202-08 chr21:47783687 G>A maps to NM_006031.5 E816E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GW-01A-11D-A202-08 chr7:44089850 C>T maps to NM_001122956.1 S37S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GW-01A-11D-A202-08 chr7:128641195 C>T maps to ENST00000471166 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GW-01A-11D-A202-08 chr9:100919703 G>A did not map to a codon.
Sequencing variant TCGA-EL-A3GX-01A-11D-A202-08 chr1:183087213 T>C maps to NM_002293.3 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GX-01A-11D-A202-08 chr19:42224845 G>A maps to NM_004363.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GY-01A-21D-A202-08 chr1:114196557 C>A maps to NM_001142782.1 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GY-01A-21D-A202-08 chr8:141549493 G>A maps to NM_012154.3 Y698Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GY-01A-21D-A202-08 chr1:160651145 A>G maps to NM_001778.2 Y166Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GY-01A-21D-A202-08 chr19:5455621 G>A maps to NM_181710.3 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GY-01A-21D-A202-08 chr8:90958471 A>G maps to NM_002485.4 L656L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GY-01A-21D-A202-08 chr4:70505148 G>A maps to ENST00000514019 I271I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GZ-01A-11D-A20C-08 chr5:139260542 G>A maps to NM_013982.2 Q297*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GZ-01A-11D-A20C-08 chr7:131195716 G>A maps to NM_001018111.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3GZ-01A-11D-A20C-08 chr11:113860391 G>T maps to NM_213621.3 V486V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H1-01A-11D-A21A-08 chrX:154003523 T>A maps to NM_001363.3 V438V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H1-01A-11D-A21A-08 chr8:37704688 G>A maps to NM_018310.3 L73L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H1-01A-11D-A21A-08 chr4:71346614 C>T maps to NM_152291.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H1-01A-11D-A21A-08 chr9:130506913 T>A maps to NM_170600.2 K577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H1-01A-11D-A21A-08 chrX:118797458 G>T maps to ENST00000394612 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H1-01A-11D-A21A-08 chr2:44055182 C>T maps to NM_022436.2 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H1-01A-11D-A21A-08 chr16:71218817 G>A maps to NM_032821.2 R71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H1-01A-11D-A21A-08 chr16:57015113 C>T maps to NM_000078.2 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H1-01A-11D-A21A-08 chrX:153668408 C>T maps to NM_001493.2 D170D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr19:18378324 G>A maps to NM_001145304.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr9:97063336 G>T maps to NM_194320.2 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr5:38448473 T>C maps to ENST00000354891 L854L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr9:131866546 G>A maps to NM_000755.3 Y110Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr6:10894116 G>A maps to NM_001040274.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr7:106851576 C>A maps to NM_006348.3 T785T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr14:75514648 T>C maps to NM_001040108.1 T570T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr19:18650450 G>A maps to NM_012181.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr21:41414504 G>A maps to NM_001389.3 L1827L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr18:28986166 T>C maps to NM_001134453.1 D588D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr12:25702463 C>A maps to NM_001145728.1 G36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr8:3165912 G>A maps to NM_033225.5 Y1248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H2-01A-11D-A20C-08 chr17:40354773 C>G did not map to a codon.
Sequencing variant TCGA-EL-A3H3-01A-11D-A202-08 chr2:150426630 G>A maps to NM_015702.2 R250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H3-01A-11D-A202-08 chr9:4662737 G>C maps to NM_203453.2 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H4-01A-11D-A202-08 chr12:121855479 C>T maps to NM_194271.1 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H4-01A-11D-A202-08 chr9:125316419 T>C maps to NM_001004457.1 S324S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H4-01A-11D-A202-08 chr3:142985758 C>A maps to NM_173653.3 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H4-01A-11D-A202-08 chr14:21108935 C>T maps to NM_001001968.1 K305K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr19:11559444 G>T did not map to a codon.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr1:27685201 G>A maps to NM_004672.3 Q861*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr1:210591548 C>T maps to NM_001170580.1 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr17:67102296 C>A maps to NM_080284.2 L815L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr1:197060036 G>A maps to NM_018136.4 R3193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chrX:17742461 T>A maps to NM_198270.2 V363V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr14:24877449 C>T maps to NM_025081.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr21:38558090 A>G did not map to a codon.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr6:33282983 G>A maps to NM_001145338.1 G570G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr15:81282071 G>A maps to NM_015154.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr17:39643689 C>T maps to NM_003771.4 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr8:12580703 T>C maps to NM_152271.3 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H5-01A-11D-A202-08 chr9:38396761 C>T maps to NM_000692.3 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H7-01A-11D-A21A-08 chr19:46278223 G>A maps to NM_004409.3 Y405Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H7-01A-11D-A21A-08 chr13:99354750 T>C maps to NM_005073.3 K483K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H7-01A-11D-A21A-08 chr8:145732032 C>T maps to NM_005309.2 R427R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H7-01A-11D-A21A-08 chr9:136915621 G>A maps to NM_007371.3 I196I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H7-01A-11D-A21A-08 chr17:59989321 G>C maps to NM_020748.2 A261A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H7-01A-11D-A21A-08 chr10:3824178 G>A maps to NM_001300.5 S110S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H7-01A-11D-A21A-08 chr2:179579857 G>A maps to NM_133378.4 S7441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H7-01A-11D-A21A-08 chr18:30349966 G>A maps to NM_020805.1 H196H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H7-01A-11D-A21A-08 chrX:47308076 A>G maps to NM_153380.2 F364F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H8-01A-11D-A20C-08 chr17:56572505 G>A maps to NM_004687.4 N999N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H8-01A-11D-A20C-08 chr6:46658464 C>A maps to NM_001010870.2 S867*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H8-01A-11D-A20C-08 chrX:154282926 C>T maps to NM_023934.3 L184L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H8-01A-11D-A20C-08 chr6:20402609 C>T maps to NM_001949.3 A49A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H8-01A-11D-A20C-08 chr19:58992083 G>A maps to NM_017908.2 E448E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H8-01A-11D-A20C-08 chr2:141245238 G>A maps to NM_018557.2 R3064*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3H8-01A-11D-A20C-08 chr15:38791142 G>A maps to NM_005739.3 C575C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MW-01A-11D-A20C-08 chr16:80718509 A>G maps to NM_152342.2 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MW-01A-11D-A20C-08 chr17:78079687 C>T maps to NM_001079804.1 R229R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MW-01A-11D-A20C-08 chr2:219299352 G>A maps to NM_007127.2 A535A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MW-01A-11D-A20C-08 chr14:50877291 G>A maps to ENST00000356146 Y37Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MW-01A-11D-A20C-08 chrX:128657221 C>T maps to NM_003069.3 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr6:37225721 G>A maps to NM_017772.2 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr3:111671549 C>T maps to NM_001134438.1 I921I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr10:127548294 A>G maps to NM_018180.2 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr7:72718829 G>A maps to NM_148956.2 D223D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr14:20859811 G>C maps to NM_007110.4 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr2:70188127 G>A maps to NM_152792.2 G231G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr7:27570873 C>A maps to NM_152740.3 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr4:4276211 G>A maps to NM_017816.2 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr22:42610591 G>A maps to NM_005650.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr2:100209824 G>C maps to NM_001025108.1 L791L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr19:2827691 C>T maps to NM_001102651.1 N68N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MX-01A-11D-A21A-08 chr1:160105252 G>A maps to NM_000702.3 G715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MY-01A-11D-A21A-08 chr16:64984727 G>A maps to NM_001797.2 N612N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MZ-01A-11D-A21A-08 chr16:3614040 C>T maps to ENST00000448023 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MZ-01A-11D-A21A-08 chr1:155932416 G>A maps to NM_001162383.1 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MZ-01A-11D-A21A-08 chr12:123805011 G>A maps to NM_001167856.1 I878I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MZ-01A-11D-A21A-08 chr3:38357109 G>T maps to NM_004803.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MZ-01A-11D-A21A-08 chr2:100623625 G>A maps to NM_001025108.1 D182D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MZ-01A-11D-A21A-08 chr7:42971805 G>A did not map to a codon.
Sequencing variant TCGA-EL-A3MZ-01A-11D-A21A-08 chr1:52499142 C>A maps to NM_138417.2 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MZ-01A-11D-A21A-08 chr1:228461983 G>A maps to NM_001098623.1 W1841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3MZ-01A-11D-A21A-08 chr12:18237558 C>T maps to NM_024730.2 W76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3N2-01A-11D-A20C-08 chr7:72861633 C>T maps to NM_032408.3 E1268E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3N2-01A-11D-A20C-08 chr12:132625899 C>T maps to NM_175066.3 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3N2-01A-11D-A20C-08 chr20:33338269 C>T maps to NM_014071.2 P576P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3N2-01A-11D-A20C-08 chr20:13850191 T>C maps to NM_025229.1 K404K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3N2-01A-11D-A20C-08 chr9:5044417 T>C maps to NM_004972.3 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3N2-01A-11D-A20C-08 chr2:187532442 G>A maps to NM_002210.3 E791E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3N2-01A-11D-A20C-08 chrX:70598837 T>C maps to ENST00000449580 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3N3-01A-11D-A20C-08 chr1:6194801 G>C maps to NM_015557.2 P996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3N3-01A-11D-A20C-08 chr3:123420310 C>T maps to NM_053025.3 Q812Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3N3-01A-11D-A20C-08 chr12:113541980 G>A maps to NM_001193520.1 T652T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T0-01A-22D-A22D-08 chr22:51044094 G>A maps to ENST00000329492 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T0-01A-22D-A22D-08 chr19:16799118 C>T maps to NM_024074.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T0-01A-22D-A22D-08 chr6:76751727 G>A maps to NM_001563.2 F61F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T0-01A-22D-A22D-08 chr20:61951641 G>A did not map to a codon.
Sequencing variant TCGA-EL-A3T0-01A-22D-A22D-08 chr2:32475707 C>A maps to NM_021209.4 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T0-01A-22D-A22D-08 chrX:20044030 C>T maps to NM_001168465.1 T349T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T0-01A-22D-A22D-08 chr6:29627258 G>A maps to NM_002433.4 K84K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T0-01A-22D-A22D-08 chr16:67862706 A>G maps to NM_025082.3 H440H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T0-01A-22D-A22D-08 chr3:183856018 C>T maps to NM_003907.2 S250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T0-01A-22D-A22D-08 chr14:45579423 G>A did not map to a codon.
Sequencing variant TCGA-EL-A3T1-01A-11D-A22D-08 chr17:37009326 C>G maps to NM_000978.3 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T1-01A-11D-A22D-08 chr17:6902318 G>A maps to NM_000697.2 W197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T1-01A-11D-A22D-08 chr7:101870708 G>T maps to ENST00000360264 E1076*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T1-01A-11D-A22D-08 chr16:67316144 G>A maps to NM_001129729.1 Q382Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T1-01A-11D-A22D-08 chr19:40319134 G>A maps to NM_004714.1 N203N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T1-01A-11D-A22D-08 chr9:130984561 G>A maps to ENST00000372923 E312E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T2-01A-11D-A22D-08 chr6:38854565 G>C did not map to a codon.
Sequencing variant TCGA-EL-A3T2-01A-11D-A22D-08 chr19:1828208 T>C maps to NM_020695.3 G193G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T2-01A-11D-A22D-08 chr7:26224961 T>C maps to NM_004289.6 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T2-01A-11D-A22D-08 chrX:24228799 G>A maps to NM_003410.3 P575P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T2-01A-11D-A22D-08 chr3:65365209 C>T maps to NM_001033057.1 E907E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T2-01A-11D-A22D-08 chr11:10064432 G>A maps to NM_030962.3 Y79Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T2-01A-11D-A22D-08 chr19:46417735 G>A maps to NM_001029861.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T2-01A-11D-A22D-08 chr14:23858159 G>A maps to NM_002471.3 R1361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T2-01A-11D-A22D-08 chr5:37001180 G>A did not map to a codon.
Sequencing variant TCGA-EL-A3T3-01A-11D-A22D-08 chrX:69253266 C>T maps to NM_001399.4 L271L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T3-01A-11D-A22D-08 chr15:76467945 G>A maps to NM_152335.2 Q233Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T3-01A-11D-A22D-08 chr13:21562775 C>A maps to NM_014572.2 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T3-01A-11D-A22D-08 chr19:40318233 G>A maps to NM_004714.1 Y290Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T3-01A-11D-A22D-08 chr11:62520400 G>A maps to NM_024784.3 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T3-01A-11D-A22D-08 chr10:113920470 G>A maps to NM_020918.4 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T3-01A-11D-A22D-08 chrX:153599580 G>A maps to NM_001110556.1 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T3-01A-11D-A22D-08 chr9:140006388 G>A maps to NM_013379.2 Y381Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T3-01A-11D-A22D-08 chr11:122659905 C>T maps to NM_032873.4 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T3-01A-11D-A22D-08 chr4:8588778 A>T did not map to a codon.
Sequencing variant TCGA-EL-A3T3-01A-11D-A22D-08 chr1:22965566 G>C maps to NM_015991.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T6-01A-11D-A21Z-08 chr4:81124556 C>T maps to NM_001099403.1 H647H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T6-01A-11D-A21Z-08 chr14:102466736 G>T did not map to a codon.
Sequencing variant TCGA-EL-A3T7-01A-11D-A22D-08 chr5:140167695 G>A maps to NM_018900.2 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T7-01A-11D-A22D-08 chr16:67424873 T>A maps to NM_016140.2 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T7-01A-11D-A22D-08 chr7:129102859 G>A maps to ENST00000450266 L569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T7-01A-11D-A22D-08 chr1:36941035 G>A maps to NM_156039.3 C101C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T7-01A-11D-A22D-08 chr3:185146740 C>A maps to NM_004721.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T8-01A-21D-A22D-08 chr11:32956670 G>A maps to NM_001076786.1 G1160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T8-01A-21D-A22D-08 chr2:178307133 G>A did not map to a codon.
Sequencing variant TCGA-EL-A3T8-01A-21D-A22D-08 chr10:7242430 C>A maps to NM_001018039.1 V501V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr2:173292653 C>T maps to ENST00000264106 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr12:89864263 G>A maps to NM_172240.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr14:59930876 G>A maps to NM_022571.5 A356A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr22:37769204 G>A maps to NM_052906.3 H790H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr3:196235045 T>C maps to NM_001077657.1 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr16:67237635 G>A maps to NM_024712.3 L726L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr19:5915242 G>A maps to ENST00000394521 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr8:145730777 G>A maps to NM_005309.2 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr1:147380579 C>A maps to NM_005267.4 I166I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chrX:68060181 G>A maps to NM_004429.4 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr12:57553704 G>A maps to NM_002332.2 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr4:123185434 C>T maps to NM_015312.3 P2390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr20:61941833 C>T maps to ENST00000326996 G462G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr16:23646582 G>T maps to NM_024675.3 V428V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr19:8576744 G>A maps to NM_001146175.1 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3T9-01A-21D-A22D-08 chr5:52360755 G>A maps to NM_002203.3 Q539Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3TA-01A-12D-A22D-08 chrX:78216607 G>T maps to NM_198333.1 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3TA-01A-12D-A22D-08 chr19:58596318 G>A maps to NM_001145542.1 F478F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3TB-01A-11D-A22D-08 chr10:43654322 C>A maps to NM_018590.3 I274I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3TB-01A-11D-A22D-08 chr5:167891807 G>A maps to NM_001161661.1 A1003A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3TB-01A-11D-A22D-08 chr5:76128980 C>T maps to NM_005242.4 H183H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3TB-01A-11D-A22D-08 chr9:137655577 G>T maps to NM_000093.3 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3TB-01A-11D-A22D-08 chr7:100685166 C>T maps to NM_001040105.1 T3490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3TB-01A-11D-A22D-08 chr11:125359607 G>A maps to NM_005103.4 D22D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZH-01A-31D-A23M-08 chrX:154305461 T>A maps to NM_024332.2 I71I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZH-01A-31D-A23M-08 chr7:72093913 C>A maps to NM_001145440.1 A525A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZH-01A-31D-A23M-08 chr22:20909295 G>C maps to NM_001003891.1 R104R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZH-01A-31D-A23M-08 chr1:16388992 C>T did not map to a codon.
Sequencing variant TCGA-EL-A3ZK-01A-21D-A23M-08 chr11:130289046 C>A maps to NM_007037.4 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZK-01A-21D-A23M-08 chrX:18807363 A>G maps to NM_006240.2 E346E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZK-01A-21D-A23M-08 chr19:39898882 G>A maps to NM_003407.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZN-01A-11D-A23M-08 chr11:100922213 T>C maps to NM_000926.4 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZN-01A-11D-A23M-08 chr19:18368856 G>A maps to NM_001145304.1 A1079A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZQ-01A-11D-A23M-08 chr1:107867091 A>C maps to NM_001113226.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZR-01A-11D-A23M-08 chr8:8998674 T>G maps to NM_024607.2 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZR-01A-11D-A23M-08 chr1:46663382 T>C maps to ENST00000371986 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZR-01A-11D-A23M-08 chr11:58126179 G>A maps to NM_001005489.1 Y121Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZR-01A-11D-A23M-08 chr14:23345000 C>T maps to NM_014045.3 Q282*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZR-01A-11D-A23M-08 chrX:19389609 C>T maps to NM_001001671.3 K1049K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZR-01A-11D-A23M-08 chr2:149528906 T>G maps to NM_015630.3 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZR-01A-11D-A23M-08 chr19:56373474 G>A maps to NM_134444.4 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZR-01A-11D-A23M-08 chr22:23401753 C>T maps to NM_014433.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZT-01A-12D-A23M-08 chr1:228210472 C>T maps to ENST00000366753 Y59Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3ZT-01A-12D-A23M-08 chr16:56906568 G>A maps to NM_000339.2 A322A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4JV-01A-11D-A257-08 chr14:89061102 T>G maps to NM_207662.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4JW-01A-11D-A257-08 chr3:128706480 G>A maps to NM_020741.2 D215D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4JW-01A-11D-A257-08 chr22:51065568 G>A did not map to a codon.
Sequencing variant TCGA-EL-A4JX-01A-12D-A257-08 chr6:119569447 A>C maps to NM_005907.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4JX-01A-12D-A257-08 chrX:18913267 C>T maps to NM_000292.2 S1108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4JZ-01A-11D-A257-08 chr17:7592187 T>C maps to NM_018081.2 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4JZ-01A-11D-A257-08 chr20:47256388 C>T maps to NM_020820.3 L1273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4JZ-01A-11D-A257-08 chr10:68687363 C>T maps to NM_178011.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4JZ-01A-11D-A257-08 chr1:114454227 G>A maps to NM_022836.3 W338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4JZ-01A-11D-A257-08 chrX:154508526 C>A maps to NM_001289.4 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4JZ-01A-11D-A257-08 chr19:58049388 A>G maps to ENST00000376233 K339K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4JZ-01A-11D-A257-08 chr1:218610804 G>C maps to NM_001135599.2 P379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K0-01A-11D-A257-08 chr3:196387347 G>C maps to NM_198565.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K2-01A-11D-A257-08 chr15:78305348 G>A maps to NM_144572.1 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K2-01A-11D-A257-08 chr5:58511658 G>A maps to NM_001104631.1 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K4-01A-11D-A257-08 chr20:39991086 C>T maps to NM_052846.1 Q374Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K6-01A-12D-A257-08 chr9:117086321 C>G maps to NM_000607.2 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K6-01A-12D-A257-08 chr12:27234343 G>A maps to ENST00000398815 I223I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K6-01A-12D-A257-08 chr7:150553563 G>A maps to ENST00000416793 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K6-01A-12D-A257-08 chr13:73345947 C>T maps to NM_014953.3 V530V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K6-01A-12D-A257-08 chr5:134785191 G>A maps to NM_001099221.1 D146D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K6-01A-12D-A257-08 chr2:179476841 G>A maps to NM_133378.4 R14198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K6-01A-12D-A257-08 chr2:48066035 A>G maps to NM_001190274.1 C183C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4K6-01A-12D-A257-08 chr7:45688321 G>A maps to NM_021116.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KD-01A-11D-A257-08 chr4:115998000 C>T maps to NM_022569.1 E64E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KD-01A-11D-A257-08 chr12:120582583 T>C maps to NM_006836.1 P1737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KD-01A-11D-A257-08 chr19:42821992 C>T maps to ENST00000406159 Q359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KD-01A-11D-A257-08 chr17:15995327 G>A maps to ENST00000395857 S971S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KD-01A-11D-A257-08 chr22:30812007 C>T maps to NM_012429.2 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KD-01A-11D-A257-08 chrX:110951557 A>G maps to NM_001099922.2 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KD-01A-11D-A257-08 chr3:130282317 C>T maps to NM_001102608.1 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KD-01A-11D-A257-08 chr19:11618515 C>T did not map to a codon.
Sequencing variant TCGA-EL-A4KD-01A-11D-A257-08 chr17:72759552 C>A maps to NM_004252.3 S217S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr1:27278145 G>T maps to NM_152365.2 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr2:85532448 G>A maps to NM_031283.2 G304G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr1:6635193 G>A maps to NM_138697.3 L334L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr7:100695159 C>A maps to NM_001040105.1 I4340I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chrX:34648443 C>A maps to NM_031442.3 E178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr11:3845542 C>G maps to NM_014489.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr9:73461348 G>C maps to ENST00000419692 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr1:23688761 G>A maps to NM_001077195.1 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr22:19118935 G>A maps to NM_053006.4 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr11:44135734 G>A maps to NM_000401.3 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr1:1269280 C>T maps to NM_152228.1 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr19:42912471 G>A maps to NM_005357.2 F474F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr11:71822276 G>A maps to NM_014042.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr6:159457890 G>C maps to NM_054114.3 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr1:151265366 G>C maps to NM_002651.2 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr19:49005817 G>C maps to NM_001080434.1 L251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr16:48155667 C>T maps to NM_033226.2 V557V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr2:67632193 T>C maps to NM_019002.3 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr3:111603724 G>A maps to NM_001134438.1 L267L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr14:105455318 C>T maps to NM_174891.3 Q155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr3:49724228 G>T maps to NM_020998.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr10:116067642 G>C maps to NM_001001936.1 L331L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr4:853444 G>A maps to NM_005255.2 Q1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr20:5904454 G>A maps to NM_001819.2 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr15:71403759 G>C maps to NM_001102658.1 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr11:67120988 G>A did not map to a codon.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr15:86205660 G>C maps to NM_006738.4 L1596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KG-01A-11D-A257-08 chr12:112701950 C>T maps to NM_001109662.2 L713L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KI-01A-11D-A257-08 chr19:11624901 C>T maps to NM_016581.3 G77G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KI-01A-11D-A257-08 chr17:19463804 C>T maps to ENST00000395585 R369*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KI-01A-11D-A257-08 chr10:73560397 C>T maps to ENST00000398860 D2461D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A4KI-01A-11D-A257-08 chr11:133801600 G>T maps to NM_014987.1 Y400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CS-01A-11D-A13W-08 chrX:100880306 C>A maps to NM_016607.3 S113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CS-01A-11D-A13W-08 chr7:100681032 G>A maps to NM_001040105.1 T2112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CS-01A-11D-A13W-08 chr6:24446030 C>A maps to NM_001503.2 E617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr8:30694874 C>T maps to NM_031271.3 V2592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr7:111484883 A>G maps to ENST00000428084 L891L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr3:58196615 G>C maps to NM_004944.2 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chrX:48403340 C>A maps to NM_002536.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr12:98927426 T>C maps to NM_003276.2 V464V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr3:180334306 T>C maps to NM_181426.1 Q861Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr12:51855026 G>A maps to NM_001039960.1 Q351Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr11:123513259 G>A maps to NM_018400.3 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr8:144940653 G>A maps to NM_031308.1 P2256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr13:20220951 A>T maps to ENST00000414242 K247*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr5:7707860 C>T maps to NM_020546.2 G437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr12:88514827 C>T maps to NM_025114.3 R435R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr14:94936075 G>A maps to NM_175739.3 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CT-01A-11D-A13W-08 chr13:101735460 C>T maps to NM_052867.2 S1224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CU-01A-11D-A13W-08 chr12:113388601 C>T maps to NM_006187.2 R493R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CU-01A-11D-A13W-08 chr21:44836662 G>A maps to NM_173354.3 L771L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CV-01A-11D-A13W-08 chr10:104353454 G>A maps to NM_016169.3 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CV-01A-11D-A13W-08 chrX:41073949 A>G maps to NM_001039590.2 K1773K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CV-01A-11D-A13W-08 chrX:135430490 A>C maps to NM_153834.3 T1542T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CV-01A-11D-A13W-08 chr9:111706097 T>A did not map to a codon.
Sequencing variant TCGA-EM-A1CV-01A-11D-A13W-08 chr2:231113618 T>A maps to NM_007237.4 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CV-01A-11D-A13W-08 chr17:48655861 C>T maps to NM_018896.3 G746G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CW-01A-21D-A13W-08 chr1:158576560 C>T maps to NM_001004478.1 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CW-01A-21D-A13W-08 chr11:47380479 G>A maps to NM_001080547.1 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CW-01A-21D-A13W-08 chr20:4768881 G>A maps to NM_014737.2 Y224Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CW-01A-21D-A13W-08 chr19:2877357 T>C maps to NM_024967.1 R134R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1CW-01A-21D-A13W-08 chr17:29508803 G>T did not map to a codon.
Sequencing variant TCGA-EM-A1CW-01A-21D-A13W-08 chr11:62287956 T>C maps to NM_001620.1 Q4644Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YA-01A-11D-A14W-08 chr9:95050406 C>G did not map to a codon.
Sequencing variant TCGA-EM-A1YA-01A-11D-A14W-08 chr15:72495520 A>G maps to ENST00000419739 R457R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YA-01A-11D-A14W-08 chr8:82606559 T>A maps to NM_001010893.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YA-01A-11D-A14W-08 chr11:18731051 G>C maps to NM_173588.3 Y960*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr17:7578274 G>A maps to NM_001126112.1 Q192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr16:1828538 G>A maps to NM_080861.3 G67G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr17:6939880 C>T maps to NM_201566.2 I60I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr10:99213323 G>C maps to NM_198046.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr15:90617454 C>T maps to NM_198526.2 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr6:142409594 G>A maps to NM_002511.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr3:127335822 C>T maps to NM_004526.2 F545F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr3:129324717 G>A maps to NM_015103.2 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr4:71634263 C>A maps to NM_001037442.2 Y194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr10:114298089 G>A did not map to a codon.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr15:33833091 G>A did not map to a codon.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr6:30121958 G>A maps to NM_006778.3 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr4:185550614 G>A maps to NM_032991.2 F215F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr6:26156746 C>T maps to NM_005321.2 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr1:197115495 C>T maps to NM_018136.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr4:144109021 G>A maps to NM_032557.5 Q242Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr8:126033113 G>A did not map to a codon.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr6:41254384 C>T maps to NM_018643.2 K3K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr5:16689985 G>A maps to NM_012334.2 I1281I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YB-01A-11D-A14W-08 chr18:10526108 C>T maps to NM_003826.2 Q4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YC-01A-11D-A14W-08 chr6:30707946 G>C maps to NM_005803.2 A237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YC-01A-11D-A14W-08 chr7:137792292 C>T maps to NM_005989.3 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YC-01A-11D-A14W-08 chr11:71943765 C>T maps to NM_001567.3 F603F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YC-01A-11D-A14W-08 chr18:30554615 T>C maps to NM_001105528.1 T806T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YC-01A-11D-A14W-08 chr12:55614960 G>A maps to NM_001005280.1 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YC-01A-11D-A14W-08 chr3:45135080 G>A maps to NM_022842.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YC-01A-11D-A14W-08 chr2:110036026 G>A maps to NM_001099289.1 T444T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YC-01A-11D-A14W-08 chr21:45483557 G>A maps to NM_003274.4 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YD-01A-11D-A14W-08 chr4:188924089 C>T maps to NM_174900.3 V43V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YD-01A-11D-A14W-08 chr2:206630289 C>T maps to NM_201266.1 C800C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YD-01A-11D-A14W-08 chr12:53225272 C>T maps to NM_175834.2 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YD-01A-11D-A14W-08 chr19:41351188 C>T did not map to a codon.
Sequencing variant TCGA-EM-A1YD-01A-11D-A14W-08 chr16:58031259 G>A maps to NM_020807.1 Q304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YE-01A-11D-A14W-08 chr5:142150380 C>T maps to NM_015071.4 R19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YE-01A-11D-A14W-08 chr1:37346337 G>A maps to NM_000831.3 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YE-01A-11D-A14W-08 chr9:125273559 C>T maps to ENST00000444856 T160T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A1YE-01A-11D-A14W-08 chr1:158225839 A>G maps to NM_001763.2 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22I-01A-11D-A17V-08 chr17:37333737 C>T maps to NM_000723.3 E399E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22I-01A-11D-A17V-08 chr21:15599325 A>G maps to NM_144770.3 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22I-01A-11D-A17V-08 chr10:85944479 G>A maps to NM_207373.2 E68E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22I-01A-11D-A17V-08 chrX:153228844 G>A maps to ENST00000369984 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22I-01A-11D-A17V-08 chr8:145113594 C>T did not map to a codon.
Sequencing variant TCGA-EM-A22J-01A-11D-A17V-08 chr5:140516257 C>T maps to NM_015669.2 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22J-01A-11D-A17V-08 chr13:49772501 C>T maps to NM_001079673.1 R927*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22J-01A-11D-A17V-08 chr5:127638773 A>G maps to NM_001999.3 D1936D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22J-01A-11D-A17V-08 chr7:100880844 T>C maps to NM_014343.2 E6E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22J-01A-11D-A17V-08 chr13:113487316 G>C maps to NM_032189.3 A513A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22J-01A-11D-A17V-08 chr2:55470597 T>C maps to NM_002453.2 K506K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22J-01A-11D-A17V-08 chr20:61524261 G>A maps to NM_033081.2 R1052*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22K-01A-11D-A17V-08 chr16:69729159 A>G maps to NM_138713.2 Q1512Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22K-01A-11D-A17V-08 chr15:40308701 G>A did not map to a codon.
Sequencing variant TCGA-EM-A22K-01A-11D-A17V-08 chr15:65677332 G>A maps to NM_020962.1 Q1101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22K-01A-11D-A17V-08 chr2:197521548 T>A maps to NM_001080539.1 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22K-01A-11D-A17V-08 chr13:42874703 A>T maps to NM_016248.2 K608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22M-01A-11D-A17V-08 chr12:55614870 C>T maps to NM_001005280.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22N-01A-11D-A17V-08 chr5:61643969 A>T maps to NM_001098511.1 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22N-01A-11D-A17V-08 chr12:111885970 G>T maps to NM_005475.2 S531S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22N-01A-11D-A17V-08 chr12:31440668 A>C maps to NM_001135812.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22O-01A-11D-A17V-08 chr2:202744822 C>T maps to ENST00000450471 S377S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22O-01A-11D-A17V-08 chr16:25182126 G>A did not map to a codon.
Sequencing variant TCGA-EM-A22O-01A-11D-A17V-08 chr15:55664156 A>G maps to ENST00000442196 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22O-01A-11D-A17V-08 chr4:169374415 T>C maps to NM_001012967.1 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22O-01A-11D-A17V-08 chr1:23743818 T>C maps to NM_003196.1 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22O-01A-11D-A17V-08 chr11:3023812 C>T maps to NM_001014437.2 R745R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22O-01A-11D-A17V-08 chr4:76886949 A>G maps to NM_018115.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22O-01A-11D-A17V-08 chr2:159519929 C>T maps to NM_003628.3 L850L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22P-01A-11D-A19J-08 chr18:24445623 C>T maps to NM_001650.4 W10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22P-01A-11D-A19J-08 chr13:21296002 G>A maps to NM_138284.1 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22P-01A-11D-A19J-08 chr1:94512587 T>C maps to NM_000350.2 V935V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22P-01A-11D-A19J-08 chr1:22033082 C>G did not map to a codon.
Sequencing variant TCGA-EM-A22P-01A-11D-A19J-08 chr6:26199950 C>T maps to NM_003522.3 I55I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22P-01A-11D-A19J-08 chr10:135098727 C>T did not map to a codon.
Sequencing variant TCGA-EM-A22P-01A-11D-A19J-08 chr1:43770795 G>A maps to NM_005424.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22Q-01A-11D-A17V-08 chr4:79360115 C>G maps to NM_025074.6 V1809V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22Q-01A-11D-A17V-08 chr11:18956322 T>A maps to NM_147199.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22Q-01A-11D-A17V-08 chr2:113332949 C>T maps to NM_019014.4 R1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22Q-01A-11D-A17V-08 chr12:56862410 C>T maps to NM_207344.3 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A22Q-01A-11D-A17V-08 chr4:146059040 A>G maps to ENST00000447906 H962H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CJ-01A-11D-A17V-08 chr17:10404033 A>G maps to NM_005963.3 D1258D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CJ-01A-11D-A17V-08 chr19:9049002 T>A maps to NM_024690.2 G10876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CJ-01A-11D-A17V-08 chrX:110951443 T>C maps to NM_001099922.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CK-01A-11D-A17V-08 chr2:182852549 C>A maps to ENST00000280295 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CK-01A-11D-A17V-08 chr17:56690783 G>A maps to ENST00000240361 R341*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CL-01A-11D-A17V-08 chr1:248263033 C>T maps to NM_175911.2 Y119Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CL-01A-11D-A17V-08 chr20:61512288 C>G maps to NM_033081.2 P1673P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CN-01A-11D-A19J-08 chr10:85972878 C>T maps to NM_033100.2 N605N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CN-01A-11D-A19J-08 chr9:133917102 G>T maps to ENST00000355048 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CN-01A-11D-A19J-08 chr16:90103674 C>T maps to NM_001481.2 H264H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CN-01A-11D-A19J-08 chr11:30033055 G>T maps to NM_002233.2 C390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CN-01A-11D-A19J-08 chr11:92577599 C>T maps to ENST00000298047 S3689S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CO-01A-11D-A19J-08 chr17:79813409 C>A maps to NM_000918.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CO-01A-11D-A19J-08 chr20:10023794 G>A maps to NM_198798.1 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CO-01A-11D-A19J-08 chr16:354423 C>T maps to NM_003502.3 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CO-01A-11D-A19J-08 chr11:1267145 G>A maps to ENST00000447027 P3015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CO-01A-11D-A19J-08 chr2:152390824 G>A maps to NM_001164507.1 Y7107Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CO-01A-11D-A19J-08 chr1:231696958 A>G maps to NM_005999.2 Q151Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CP-01A-11D-A17V-08 chrX:150869381 C>T maps to NM_024082.3 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CP-01A-11D-A17V-08 chr2:219561865 A>G maps to NM_015690.3 A897A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CQ-01A-11D-A17V-08 chr6:32037913 G>A maps to ENST00000375244 D1756D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CQ-01A-11D-A17V-08 chr3:3189628 C>T maps to NM_182916.2 L366L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CQ-01A-11D-A17V-08 chr3:77626738 C>T maps to ENST00000332191 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CR-01A-11D-A17V-08 chrX:141291128 G>A maps to NM_016249.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CR-01A-11D-A17V-08 chr19:44500959 G>A maps to NM_003445.2 R317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CR-01A-11D-A17V-08 chr3:183041037 C>T maps to NM_015078.2 W196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CR-01A-11D-A17V-08 chr20:1551538 C>T maps to NM_006065.3 V332V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CT-01A-11D-A17V-08 chr18:54603137 T>C did not map to a codon.
Sequencing variant TCGA-EM-A2CU-01A-12D-A17V-08 chr16:845755 C>T maps to ENST00000317063 R958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CU-01A-12D-A17V-08 chr1:23645158 G>A maps to ENST00000414299 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CU-01A-12D-A17V-08 chrX:135827438 G>A maps to NM_004840.2 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CU-01A-12D-A17V-08 chr1:62550207 C>G maps to NM_176877.2 S1422*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2CU-01A-12D-A17V-08 chr5:129520923 A>T maps to NM_175856.4 R697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OV-01A-11D-A202-08 chr16:2331126 G>A maps to NM_001089.2 A1420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OV-01A-11D-A202-08 chr10:95849060 C>T maps to NM_001165979.1 F70F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OV-01A-11D-A202-08 chr4:144466690 A>G maps to NM_003601.2 L784L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OV-01A-11D-A202-08 chr12:110765416 C>T maps to NM_170665.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OV-01A-11D-A202-08 chr1:152275655 G>A maps to NM_002016.1 P3902P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OW-01A-11D-A202-08 chr9:119770422 G>A maps to ENST00000313400 L513L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OW-01A-11D-A202-08 chr4:105412389 C>T maps to NM_025212.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OW-01A-11D-A202-08 chr19:45397110 C>T maps to NM_006114.2 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OW-01A-11D-A202-08 chr16:77401461 G>A maps to NM_199355.2 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OW-01A-11D-A202-08 chr13:108518545 G>C maps to NM_001080396.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OW-01A-11D-A202-08 chr4:77637503 T>C maps to ENST00000380735 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OW-01A-11D-A202-08 chr1:67705964 G>A did not map to a codon.
Sequencing variant TCGA-EM-A2OW-01A-11D-A202-08 chr11:55371141 G>A maps to NM_001004700.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OX-01A-11D-A202-08 chr16:31374647 C>T maps to NM_000887.3 L555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OX-01A-11D-A202-08 chr1:179112140 A>G maps to NM_005158.4 Y13Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OX-01A-11D-A202-08 chr9:5029858 C>T maps to NM_004972.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OX-01A-11D-A202-08 chr10:101953149 T>C maps to NM_001278.3 L671L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OY-01A-11D-A202-08 chr12:1940260 G>A maps to NM_001163926.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr2:241402795 C>G maps to NM_002081.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr16:53968000 G>A maps to NM_001080432.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr10:79593778 C>G maps to NM_004747.3 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr15:51984516 G>A maps to NM_013243.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr2:27535567 C>T maps to ENST00000405983 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr14:105418952 C>G maps to NM_138420.2 L945L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr5:37173961 A>C maps to NM_023073.3 A2022A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr10:131506230 G>A maps to NM_002412.3 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr3:142840197 C>T maps to NM_004267.3 F180F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr4:159789775 C>G maps to ENST00000379346 S686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr3:159713291 C>T maps to NM_000882.2 F236F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr2:215819925 C>T maps to NM_173076.2 P2131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr7:44575962 C>T maps to NM_013389.2 G582G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr13:32747676 G>A maps to NM_023037.2 G775G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2OZ-01A-11D-A202-08 chr20:2552905 G>A maps to NM_080751.2 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P0-01A-11D-A202-08 chr6:38980291 G>A maps to ENST00000327475 W4519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P1-01A-11D-A202-08 chr3:142037637 T>C maps to NM_019001.3 Q1503Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P1-01A-11D-A202-08 chr22:47059055 C>T maps to NM_015124.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P1-01A-11D-A202-08 chr1:34128589 C>T maps to ENST00000373381 P1345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P2-01A-11D-A202-08 chr4:107216252 C>T maps to NM_001163436.1 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P2-01A-11D-A202-08 chr9:117052335 A>G did not map to a codon.
Sequencing variant TCGA-EM-A2P3-01A-11D-A202-08 chr20:306861 C>T maps to NM_006943.2 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P3-01A-11D-A202-08 chr1:31845843 C>A maps to NM_004102.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P3-01A-11D-A202-08 chr22:50436468 G>A maps to NM_001001694.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A2P3-01A-11D-A202-08 chr4:186578640 T>C maps to ENST00000355634 K168K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AI-01A-11D-A202-08 chr11:70282507 C>T maps to NM_001184740.1 C633C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AI-01A-11D-A202-08 chr14:21238576 C>T maps to NM_022360.4 R90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AI-01A-11D-A202-08 chr12:131484926 G>C did not map to a codon.
Sequencing variant TCGA-EM-A3AI-01A-11D-A202-08 chr17:7612770 C>T maps to NM_001406.3 G300G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AI-01A-11D-A202-08 chr14:105409976 G>A maps to NM_138420.2 D3937D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AI-01A-11D-A202-08 chrX:131205245 G>A did not map to a codon.
Sequencing variant TCGA-EM-A3AJ-01A-11D-A202-08 chr16:77396027 C>T maps to NM_199355.2 W397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AJ-01A-11D-A202-08 chr6:30128709 T>C did not map to a codon.
Sequencing variant TCGA-EM-A3AJ-01A-11D-A202-08 chr12:106460870 G>A maps to NM_014840.2 Y565Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AJ-01A-11D-A202-08 chr1:9783254 C>G maps to ENST00000361110 T857T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AK-01A-11D-A202-08 chr16:1831285 A>G did not map to a codon.
Sequencing variant TCGA-EM-A3AK-01A-11D-A202-08 chr8:142231784 A>T maps to NM_001080431.1 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AK-01A-11D-A202-08 chr3:16254128 C>T maps to NM_054110.4 H417H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AK-01A-11D-A202-08 chr19:860953 C>A maps to NM_001928.2 P102P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AK-01A-11D-A202-08 chr19:12502821 T>C maps to NM_001080821.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AL-01A-11D-A202-08 chr5:44809123 C>T maps to NM_016640.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AL-01A-11D-A202-08 chr17:55918340 C>G maps to NM_016070.3 G122G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AL-01A-11D-A202-08 chr18:32374190 C>T maps to NM_001390.4 N113N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AL-01A-11D-A202-08 chr14:105212621 T>G maps to NM_199165.1 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AL-01A-11D-A202-08 chr8:53084924 C>A maps to NM_014682.2 E166*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AL-01A-11D-A202-08 chrX:107869595 A>G did not map to a codon.
Sequencing variant TCGA-EM-A3AL-01A-11D-A202-08 chrX:12837724 C>T maps to NM_001039091.2 D213D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AL-01A-11D-A202-08 chr17:30615974 C>T maps to NM_138328.2 Y153Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AL-01A-11D-A202-08 chr21:41648054 G>A maps to NM_001389.3 D775D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AL-01A-11D-A202-08 chr15:34537937 G>A maps to NM_133647.1 L594L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AN-01A-11D-A202-08 chr4:149075796 G>C maps to ENST00000511528 S761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AN-01A-11D-A202-08 chr1:14059319 A>G maps to NM_012231.4 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AN-01A-11D-A202-08 chr18:30349945 C>T maps to NM_020805.1 K203K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AO-01A-11D-A202-08 chr11:57075942 G>A maps to NM_033396.2 Y1414Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AO-01A-11D-A202-08 chr18:77659599 G>A maps to NM_012283.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AP-01A-12D-A20C-08 chr11:1094842 C>T maps to ENST00000441003 N1977N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AP-01A-12D-A20C-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AP-01A-12D-A20C-08 chr6:46849817 T>C maps to NM_015234.4 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AP-01A-12D-A20C-08 chr10:115978233 A>G maps to NM_198795.1 V795V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AP-01A-12D-A20C-08 chr8:139890068 G>A maps to NM_152888.1 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AQ-01A-11D-A20C-08 chr22:18604301 C>T maps to NM_018943.2 C20C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AQ-01A-11D-A20C-08 chr19:4219656 C>T maps to ENST00000262970 Q1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AQ-01A-11D-A20C-08 chr4:146059040 A>G maps to ENST00000447906 H962H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AQ-01A-11D-A20C-08 chr7:119915765 C>T maps to NM_012281.2 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AR-01A-12D-A20C-08 chr9:116930152 C>T maps to NM_032888.2 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AR-01A-12D-A20C-08 chr16:46764580 C>A maps to NM_182493.2 E498*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3AR-01A-12D-A20C-08 chr2:44099166 G>A maps to NM_022437.2 R339R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FJ-01A-11D-A21A-08 chr12:70723332 G>T maps to NM_014515.5 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FL-01A-11D-A21A-08 chr1:95290098 C>T maps to NM_001114106.1 L62L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FL-01A-11D-A21A-08 chr12:64810531 C>A maps to NM_007235.3 Y66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FL-01A-11D-A21A-08 chr7:131012678 C>T maps to NM_013255.4 V7V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FL-01A-11D-A21A-08 chr9:102713484 A>G maps to NM_017919.2 E111E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FL-01A-11D-A21A-08 chr14:68274319 G>A maps to NM_015346.3 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FL-01A-11D-A21A-08 chr2:27426732 G>A maps to NM_021095.2 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FL-01A-11D-A21A-08 chr1:22447974 G>A maps to NM_030761.4 C136C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FL-01A-11D-A21A-08 chr6:160205734 G>A maps to NM_030752.2 I211I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FL-01A-11D-A21A-08 chr4:186291862 G>A maps to ENST00000362004 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FL-01A-11D-A21A-08 chr19:46124494 G>T maps to NM_001193268.1 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FM-01A-11D-A21A-08 chr3:121616259 T>C maps to NM_021082.3 Y73Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FM-01A-11D-A21A-08 chr15:86270358 G>A maps to NM_006738.4 E2299E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FM-01A-11D-A21A-08 chr5:40937652 G>T did not map to a codon.
Sequencing variant TCGA-EM-A3FM-01A-11D-A21A-08 chr11:71238543 C>T maps to NM_001012503.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FM-01A-11D-A21A-08 chr19:12297910 C>T maps to NM_003437.3 R240*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FN-01A-11D-A21A-08 chrX:84363500 G>A maps to NM_001012980.2 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FN-01A-11D-A21A-08 chr7:18688245 G>A maps to NM_178425.2 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FN-01A-11D-A21A-08 chr15:43712830 G>T maps to NM_001141980.1 S1451S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FN-01A-11D-A21A-08 chr21:46078030 C>T maps to NM_198697.2 C45C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FN-01A-11D-A21A-08 chr12:4791379 G>A maps to NM_005002.4 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FN-01A-11D-A21A-08 chr6:159184418 C>G maps to ENST00000297239 S534*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FO-01A-11D-A21A-08 chr2:160289577 A>G maps to NM_013450.2 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FO-01A-11D-A21A-08 chr7:129666091 G>T maps to NM_016478.3 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FO-01A-11D-A21A-08 chr14:102484913 G>A maps to NM_001376.4 P2768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FO-01A-11D-A21A-08 chr18:61569115 G>A maps to NM_001143818.1 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FO-01A-11D-A21A-08 chr6:132171139 C>A maps to NM_006208.2 C108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FP-01A-11D-A21A-08 chrX:153763438 G>C maps to ENST00000369620 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FP-01A-11D-A21A-08 chr6:32135284 C>T maps to NM_030652.2 A229A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FP-01A-11D-A21A-08 chr1:84967625 G>A maps to NM_005274.2 Q37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FP-01A-11D-A21A-08 chr11:4825376 G>A maps to ENST00000380382 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FQ-01A-11D-A21A-08 chr13:113728877 G>A did not map to a codon.
Sequencing variant TCGA-EM-A3FQ-01A-11D-A21A-08 chr7:98254300 C>G maps to NM_002523.2 Y237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FQ-01A-11D-A21A-08 chr12:126138655 G>A maps to NM_052907.2 P879P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FQ-01A-11D-A21A-08 chr16:51173858 A>G maps to ENST00000251020 A758A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FR-01A-11D-A21Z-08 chr15:40268677 C>A maps to NM_001013703.2 R628R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FR-01A-11D-A21Z-08 chr12:50050233 G>A maps to NM_175736.4 R280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FR-01A-11D-A21Z-08 chr17:43311540 G>A maps to NM_005892.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FR-01A-11D-A21Z-08 chr5:140180925 C>A maps to NM_018906.2 I48I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3FR-01A-11D-A21Z-08 chr2:136574958 G>A maps to NM_002299.2 T553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O3-01A-11D-A21Z-08 chr20:25507166 G>A maps to NM_025176.4 C19C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O3-01A-11D-A21Z-08 chr10:99498332 A>G maps to NM_001002261.3 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O3-01A-11D-A21Z-08 chr1:151020355 C>T maps to NM_017860.3 V11V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O3-01A-11D-A21Z-08 chr1:228465533 A>G maps to NM_001098623.1 E2278E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O3-01A-11D-A21Z-08 chr5:176311065 A>G maps to NM_002115.2 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O3-01A-11D-A21Z-08 chr6:51921514 G>A maps to NM_138694.3 L558L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O3-01A-11D-A21Z-08 chr19:4498372 G>A maps to ENST00000301284 P491P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-EM-A3O3-01A-11D-A21Z-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EM-A3O3-01A-11D-A21Z-08 chr11:1269179 C>A maps to ENST00000447027 T3693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O3-01A-11D-A21Z-08 chr17:293074 C>T maps to NM_182705.2 K105K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O3-01A-11D-A21Z-08 chr1:149943018 G>A maps to NM_020205.2 I82I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O3-01A-11D-A21Z-08 chr5:70800540 C>T maps to NM_018429.2 Q779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O6-01A-11D-A21Z-08 chr1:247264278 T>G maps to NM_024804.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O6-01A-11D-A21Z-08 chr13:110857849 T>C maps to NM_001845.4 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O6-01A-11D-A21Z-08 chrX:54048690 C>A did not map to a codon.
Sequencing variant TCGA-EM-A3O6-01A-11D-A21Z-08 chr8:113259315 G>A maps to NM_198123.1 L3385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O6-01A-11D-A21Z-08 chr1:10713461 G>A maps to NM_001079843.1 A884A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O6-01A-11D-A21Z-08 chr22:42610591 G>A maps to NM_005650.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O6-01A-11D-A21Z-08 chr1:116929944 G>A maps to NM_000701.7 A73A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O6-01A-11D-A21Z-08 chr3:47859528 C>T maps to NM_138615.2 Q16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O7-01A-11D-A21Z-08 chr2:179997120 T>C maps to NM_178123.4 E294E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O7-01A-11D-A21Z-08 chr6:54805630 C>A maps to NM_001010872.1 S621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O7-01A-11D-A21Z-08 chr2:175437076 C>T maps to NM_003387.4 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O7-01A-11D-A21Z-08 chr2:131521450 G>A maps to NM_001105195.1 E602E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O7-01A-11D-A21Z-08 chr1:151196718 A>G did not map to a codon.
Sequencing variant TCGA-EM-A3O7-01A-11D-A21Z-08 chr1:155932416 G>A maps to NM_001162383.1 Y356Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O7-01A-11D-A21Z-08 chr12:11149658 T>C maps to NM_176889.2 P272P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O7-01A-11D-A21Z-08 chr11:60695171 C>G maps to NM_017870.3 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O7-01A-11D-A21Z-08 chr17:48271723 G>A maps to NM_000088.3 L534L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O7-01A-11D-A21Z-08 chr3:45533061 G>A maps to NM_015340.3 R431R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O7-01A-11D-A21Z-08 chr14:103148315 G>T did not map to a codon.
Sequencing variant TCGA-EM-A3O8-01A-11D-A21Z-08 chr1:113234305 G>T maps to NM_020963.3 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O8-01A-11D-A21Z-08 chr4:186295504 T>C maps to ENST00000362004 K149K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O8-01A-11D-A21Z-08 chr10:104139191 G>A did not map to a codon.
Sequencing variant TCGA-EM-A3O8-01A-11D-A21Z-08 chr9:97063303 C>T maps to NM_194320.2 C488C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O8-01A-11D-A21Z-08 chrX:75648745 G>A maps to NM_020932.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O8-01A-11D-A21Z-08 chr1:35580760 C>A maps to NM_024772.3 A1110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O9-01A-11D-A21Z-08 chr5:23524562 T>A maps to NM_020227.2 Y357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O9-01A-11D-A21Z-08 chr19:50940752 C>T maps to NM_004533.3 Q163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3O9-01A-11D-A21Z-08 chr11:105795387 C>T maps to NM_000829.3 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OA-01A-11D-A21Z-08 chr8:53580651 G>T maps to NM_014781.4 R368R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OA-01A-11D-A21Z-08 chr8:120114629 A>G maps to NM_006438.3 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OA-01A-11D-A21Z-08 chr20:32026781 A>G maps to NM_003098.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OA-01A-11D-A21Z-08 chr16:30594123 G>A maps to NM_152458.6 S325S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OA-01A-11D-A21Z-08 chr17:79952714 C>T maps to ENST00000306729 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OA-01A-11D-A21Z-08 chr6:133073822 G>A maps to NM_004665.2 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OA-01A-11D-A21Z-08 chr10:64973723 G>A maps to NM_032776.1 Q735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OA-01A-11D-A21Z-08 chr7:103197508 C>A maps to ENST00000428762 T1904T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OA-01A-11D-A21Z-08 chr9:128001312 A>G maps to NM_005347.4 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OA-01A-11D-A21Z-08 chr19:40318194 A>G maps to NM_004714.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OA-01A-11D-A21Z-08 chr9:137630644 T>A maps to NM_000093.3 P495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OB-01A-11D-A21Z-08 chr17:7604997 G>A maps to NM_018081.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OB-01A-11D-A21Z-08 chr12:64812807 C>G maps to NM_007235.3 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OB-01A-11D-A21Z-08 chr17:18023163 C>T maps to ENST00000205890 D350D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OB-01A-11D-A21Z-08 chrX:154490294 G>A maps to NM_171998.2 Y145Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OB-01A-11D-A21Z-08 chr18:3187545 C>A maps to NM_003803.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OB-01A-11D-A21Z-08 chr17:72945405 C>A maps to NM_178233.1 Y562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A3OB-01A-11D-A21Z-08 chr5:140209346 C>T maps to NM_018909.2 D557D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FK-01A-11D-A257-08 chr11:6653562 T>G maps to NM_003737.2 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FK-01A-11D-A257-08 chr1:185834991 T>C maps to NM_031935.2 N206N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FM-01A-11D-A257-08 chr17:78343412 T>C maps to NM_020914.4 I4138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FM-01A-11D-A257-08 chr15:49081162 C>A maps to NM_001194998.1 L336L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FM-01A-11D-A257-08 chr17:62265587 G>A maps to NM_018469.3 S795S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FM-01A-11D-A257-08 chrX:41058004 T>C did not map to a codon.
Sequencing variant TCGA-EM-A4FM-01A-11D-A257-08 chr21:45837905 G>A maps to ENST00000397932 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FM-01A-11D-A257-08 chr16:80638350 G>C maps to NM_152342.2 L485L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FO-01A-11D-A257-08 chr9:34241442 G>A maps to NM_001171201.1 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FO-01A-11D-A257-08 chr1:160109743 C>T maps to NM_000702.3 R1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FO-01A-11D-A257-08 chr20:25198163 C>T maps to NM_001247.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FO-01A-11D-A257-08 chr18:70417313 G>A maps to NM_153181.2 H507H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FO-01A-11D-A257-08 chr7:66774112 T>C maps to NM_022906.2 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FQ-01A-11D-A257-08 chr16:56782201 C>T maps to NM_014669.3 Q15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FQ-01A-11D-A257-08 chr1:171249977 G>A maps to NM_002021.1 S227S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FR-01A-11D-A257-08 chr16:19070963 C>T did not map to a codon.
Sequencing variant TCGA-EM-A4FV-01A-11D-A257-08 chr6:29591189 T>G maps to NM_001470.2 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FV-01A-11D-A257-08 chr12:110812080 C>T maps to NM_016238.2 E556E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FV-01A-11D-A257-08 chr19:36686016 C>T maps to ENST00000355114 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FV-01A-11D-A257-08 chrX:20148725 C>G did not map to a codon.
Sequencing variant TCGA-EM-A4FV-01A-11D-A257-08 chr1:33745737 C>T maps to NM_152493.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FV-01A-11D-A257-08 chr19:53762044 C>T maps to NM_173856.2 I139I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FV-01A-11D-A257-08 chr11:124180035 C>T maps to NM_001002917.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FV-01A-11D-A257-08 chr1:79383542 C>A maps to NM_022159.3 G552*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4FV-01A-11D-A257-08 chr10:1046798 C>T maps to NM_012341.2 F279F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EM-A4G1-01A-11D-A257-08 chr6:7231937 C>T maps to NM_001003699.3 D1202D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25G-01A-11D-A16O-08 chr7:44805071 C>G maps to NM_031449.3 L712L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25G-01A-11D-A16O-08 chr1:86959122 C>T maps to NM_001285.3 I507I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25G-01A-11D-A16O-08 chr8:110396356 G>A did not map to a codon.
Sequencing variant TCGA-ET-A25I-01A-11D-A16O-08 chr2:74274198 T>C maps to ENST00000409262 P292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25I-01A-11D-A16O-08 chrX:153033717 G>A maps to NM_005393.2 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25I-01A-11D-A16O-08 chr12:58131102 G>A maps to NM_001122772.1 S309S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25I-01A-11D-A16O-08 chr1:41582674 C>T maps to NM_001031694.2 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25I-01A-11D-A16O-08 chr9:135275451 A>G maps to NM_007344.2 L521L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25I-01A-11D-A16O-08 chr5:140209538 G>A maps to NM_018909.2 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25J-01A-11D-A16O-08 chr6:42796797 C>T maps to NM_015349.1 Q243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25J-01A-11D-A16O-08 chr2:135745372 G>A maps to NM_025052.3 R357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25J-01A-11D-A16O-08 chr3:72890282 G>C maps to NM_018130.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25J-01A-11D-A16O-08 chr7:4008967 C>A maps to NM_152744.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25J-01A-11D-A16O-08 chr6:41162467 A>G maps to ENST00000373108 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25K-01A-11D-A16O-08 chr1:34190210 G>A maps to ENST00000373381 T890T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25K-01A-11D-A16O-08 chr2:109382493 T>G maps to NM_006267.4 S1833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25K-01A-11D-A16O-08 chr20:62592688 T>C maps to NM_020713.1 K800K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25K-01A-11D-A16O-08 chr17:5253768 C>T maps to NM_004703.4 R270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25O-01A-11D-A17V-08 chr10:103921612 A>T maps to ENST00000405356 P634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25R-01A-11D-A17V-08 chr10:15646257 A>G maps to NM_003638.1 F689F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25R-01A-11D-A17V-08 chr1:145561415 C>T maps to NM_144698.3 G368G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25R-01A-11D-A17V-08 chr4:177095770 T>C maps to NM_170710.4 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A25R-01A-11D-A17V-08 chr5:89979770 C>T maps to NM_032119.3 V2011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr17:79857211 C>T maps to NM_001002244.1 I68I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr1:179077268 G>A maps to NM_007314.3 Q1045*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr14:95058527 C>T maps to NM_000624.4 F391F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr7:148767889 C>T maps to NM_152411.3 V658V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr6:109322622 G>A maps to NM_014454.1 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr2:152320158 G>A maps to NM_018151.4 E1375E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr11:70007785 G>A maps to NM_018043.5 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr11:65349702 G>C maps to NM_001099409.1 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr2:54014409 C>T maps to NM_015701.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr15:44630078 C>G maps to NM_138423.3 S232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr9:131397415 G>A maps to NM_052844.3 F312F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr6:99924036 C>G maps to NM_001080481.1 V305V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr17:40271402 G>A maps to NM_021078.2 Y311Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr2:27822492 G>A maps to NM_032434.2 Q107Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr20:50071157 G>A maps to NM_012340.3 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr8:12594451 C>G maps to NM_152271.3 V437V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr11:66407596 G>A did not map to a codon.
Sequencing variant TCGA-ET-A2MZ-01A-12D-A19J-08 chr8:37693172 G>A maps to NM_032777.9 L645L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N0-01A-11D-A18F-08 chr1:159799719 G>T maps to NM_020125.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N0-01A-11D-A18F-08 chrX:154250784 G>A maps to NM_000132.3 R15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N0-01A-11D-A18F-08 chr3:150398570 T>C maps to NM_152394.3 K343K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N0-01A-11D-A18F-08 chr18:9126839 A>G maps to NM_021074.4 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N1-01A-11D-A18F-08 chr19:49116551 T>C maps to NM_017708.3 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N1-01A-11D-A18F-08 chr15:24923275 G>A maps to NM_018958.2 R754R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N1-01A-11D-A18F-08 chr17:47583934 G>A maps to NM_002507.3 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N4-01A-12D-A19J-08 chr16:74530416 C>T maps to NM_012201.5 E300E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N4-01A-12D-A19J-08 chr7:94058708 G>A maps to NM_000089.3 R1307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N4-01A-12D-A19J-08 chr16:57718005 C>T maps to NM_170776.4 F348F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N4-01A-12D-A19J-08 chr12:109614052 G>T maps to NM_001093.3 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N4-01A-12D-A19J-08 chr11:134080346 G>A maps to NM_015261.2 G128G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N5-01A-11D-A18F-08 chr4:1985180 C>T maps to NM_005663.3 E495E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N5-01A-11D-A18F-08 chr12:70948967 G>T maps to NM_001109754.1 Y1705*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2N5-01A-11D-A18F-08 chr19:51919498 T>C did not map to a codon.
Sequencing variant TCGA-ET-A39I-01A-11D-A19J-08 chr2:170367328 A>T maps to NM_006063.2 I347I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39I-01A-11D-A19J-08 chr17:65941715 G>T maps to ENST00000321892 E2424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39I-01A-11D-A19J-08 chr2:85536171 A>T maps to NM_031283.2 K452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39I-01A-11D-A19J-08 chr19:49812976 G>A maps to NM_014037.2 V269V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39J-01A-11D-A19J-08 chr3:48668078 A>G maps to NM_022911.2 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39J-01A-11D-A19J-08 chr1:158583509 C>T did not map to a codon.
Sequencing variant TCGA-ET-A39K-01A-11D-A19J-08 chr17:27208389 C>T maps to ENST00000394906 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39K-01A-11D-A19J-08 chr1:63991289 C>A maps to NM_032437.2 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39L-01A-12D-A19J-08 chr1:203816375 C>T maps to NM_014827.4 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39M-01A-11D-A19J-08 chr7:102110078 C>T maps to NM_152892.1 Y429Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39M-01A-11D-A19J-08 chr16:3016731 C>T maps to NM_172229.1 D192D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39M-01A-11D-A19J-08 chr3:14861537 C>T maps to NM_152536.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39M-01A-11D-A19J-08 chr11:72945650 C>T maps to NM_176071.1 Y149Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39M-01A-11D-A19J-08 chr22:17583104 C>T maps to NM_014339.5 N225N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39M-01A-11D-A19J-08 chr1:20009577 G>A maps to NM_181719.4 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39M-01A-11D-A19J-08 chr8:144671276 G>A maps to NM_032378.4 A325A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39M-01A-11D-A19J-08 chr7:107752269 C>T maps to NM_007356.2 W105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39N-01A-11D-A19J-08 chr5:56180601 G>T maps to NM_005921.1 G1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39N-01A-11D-A19J-08 chr4:119944587 C>T maps to NM_133477.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39N-01A-11D-A19J-08 chr16:341239 C>T maps to NM_003502.3 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39O-01A-11D-A19J-08 chr1:179887368 T>C maps to ENST00000398836 L584L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39O-01A-11D-A19J-08 chr19:42471324 G>T maps to ENST00000441343 S1030*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39O-01A-11D-A19J-08 chrX:99933583 G>A maps to NM_001129896.2 P557P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39O-01A-11D-A19J-08 chr17:4443213 G>A maps to NM_001105538.1 T1161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39O-01A-11D-A19J-08 chr14:69522319 G>A maps to NM_003861.2 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39O-01A-11D-A19J-08 chr4:174169177 A>G maps to NM_017423.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39P-01A-21D-A19J-08 chr3:10413501 G>C maps to NM_001001331.2 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39P-01A-21D-A19J-08 chr2:27666262 A>C did not map to a codon.
Sequencing variant TCGA-ET-A39P-01A-21D-A19J-08 chr1:92711146 T>G maps to NM_001012425.1 A153A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-ET-A39P-01A-21D-A19J-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-ET-A39P-01A-21D-A19J-08 chr10:15688983 T>C maps to NM_003638.1 E356E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39P-01A-21D-A19J-08 chr12:55615053 T>A maps to NM_001005280.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39R-01A-11D-A19J-08 chr2:227663265 C>A maps to NM_005544.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39S-01A-11D-A19J-08 chr17:3518730 T>C maps to NM_013276.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39T-01A-11D-A19J-08 chr11:6461364 A>C did not map to a codon.
Sequencing variant TCGA-ET-A39T-01A-11D-A19J-08 chrX:1540712 C>T maps to NM_004192.3 A361A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39T-01A-11D-A19J-08 chr2:29474116 G>A maps to NM_004304.3 T686T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39T-01A-11D-A19J-08 chr11:428730 G>A maps to NM_001012302.2 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39T-01A-11D-A19J-08 chr8:55538949 G>T maps to NM_006269.1 P836P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A39T-01A-11D-A19J-08 chr20:44463078 C>A maps to NM_033421.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BN-01A-11D-A19J-08 chr11:85436917 A>G maps to ENST00000359152 L718L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BN-01A-11D-A19J-08 chr12:123472876 G>A maps to NM_020845.2 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BO-01A-11D-A19J-08 chr2:33335733 C>T maps to ENST00000354476 Q317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BO-01A-11D-A19J-08 chr19:14992047 G>A maps to NM_030901.1 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BP-01A-21D-A19J-08 chr16:10524629 G>A maps to NM_024997.2 Q51Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BQ-01B-11D-A202-08 chrX:153585850 G>A maps to NM_001110556.1 Y1632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BQ-01B-11D-A202-08 chr1:108292101 G>A maps to NM_006113.4 T458T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BS-01A-11D-A202-08 chr2:101598736 A>G maps to NM_002518.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BS-01A-11D-A202-08 chr1:46501482 C>T maps to NM_015112.2 A1714A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BS-01A-11D-A202-08 chr12:98991695 T>G maps to NM_213611.2 G114G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BS-01A-11D-A202-08 chr5:38511958 G>A maps to NM_002310.5 Y223Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BT-01A-11D-A19J-08 chr9:8454578 C>A did not map to a codon.
Sequencing variant TCGA-ET-A3BT-01A-11D-A19J-08 chr3:142031580 C>T maps to NM_019001.3 S1559S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BT-01A-11D-A19J-08 chr18:9588149 G>A maps to NM_001042388.1 C174C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BT-01A-11D-A19J-08 chr17:2203562 G>T maps to NM_017575.4 R162R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BT-01A-11D-A19J-08 chr18:28602424 C>T maps to NM_001941.3 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BT-01A-11D-A19J-08 chr18:21660662 T>A maps to NM_001135993.1 L192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BU-01A-11D-A19J-08 chr17:71282216 G>A maps to NM_012121.4 S141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BU-01A-11D-A19J-08 chr17:27910004 G>A maps to NM_001085454.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BV-01A-11D-A19J-08 chr2:223789307 C>T maps to NM_203372.1 C429C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BV-01A-11D-A19J-08 chr3:58849301 G>T maps to ENST00000482387 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BV-01A-11D-A19J-08 chr11:66472832 C>T maps to NM_006946.2 E638E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BV-01A-11D-A19J-08 chr16:4924498 T>G maps to NM_016936.3 P696P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BV-01A-11D-A19J-08 chr17:72938089 C>T maps to NM_178233.1 D195D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BV-01A-11D-A19J-08 chr8:8176173 G>A maps to NM_001080826.1 P1237P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BV-01A-11D-A19J-08 chr2:188332579 A>G maps to NM_006287.4 N236N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BW-01A-11D-A19J-08 chr19:16199867 C>T maps to NM_001145160.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BW-01A-11D-A19J-08 chr8:38287335 C>T maps to NM_001174067.1 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BW-01A-11D-A19J-08 chr9:127999359 A>C maps to NM_005347.4 R492R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BW-01A-11D-A19J-08 chr2:179610554 A>G maps to ENST00000375038 Y5526Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DO-01A-11D-A19J-08 chr1:41486323 G>C maps to NM_144990.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DO-01A-11D-A19J-08 chr8:145009392 C>A maps to NM_201380.2 G368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DO-01A-11D-A19J-08 chrX:118585974 C>T maps to NM_145305.2 Q232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DO-01A-11D-A19J-08 chr16:1591952 G>A maps to NM_024600.4 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DO-01A-11D-A19J-08 chr19:56363697 C>T maps to NM_134444.4 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DP-01A-11D-A21A-08 chr20:45891128 G>A maps to ENST00000471951 S508S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DP-01A-11D-A21A-08 chr1:907716 C>T maps to ENST00000379409 Y357Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DP-01A-11D-A21A-08 chr14:24676435 T>C maps to NM_001184739.1 S185S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DP-01A-11D-A21A-08 chr3:49866893 C>T maps to NM_005879.2 Q428Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DP-01A-11D-A21A-08 chr10:114911637 C>A maps to NM_030756.4 R363R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DP-01A-11D-A21A-08 chr17:49067104 C>A maps to ENST00000376407 E917*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DQ-01A-11D-A19J-08 chr6:139694454 G>T maps to NM_006079.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DQ-01A-11D-A19J-08 chr10:115481473 G>T maps to NM_033338.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DQ-01A-11D-A19J-08 chr5:272943 T>C did not map to a codon.
Sequencing variant TCGA-ET-A3DQ-01A-11D-A19J-08 chr17:4643963 C>A maps to NM_001136046.1 R41R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DR-01A-11D-A19J-08 chr1:154101783 G>A maps to NM_207308.2 C349C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DR-01A-11D-A19J-08 chr6:148840737 C>G maps to NM_015278.3 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DR-01A-11D-A19J-08 chr3:151129079 C>T maps to NM_053002.4 G1940G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DR-01A-11D-A19J-08 chr7:104715088 G>T did not map to a codon.
Sequencing variant TCGA-ET-A3DR-01A-11D-A19J-08 chr5:127674745 G>A maps to NM_001999.3 D1117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DS-01A-11D-A19J-08 chr14:81609808 C>A maps to NM_000369.2 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DS-01A-11D-A19J-08 chr10:93748981 T>C maps to NM_003972.2 S833S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DS-01A-11D-A19J-08 chrX:135427193 C>T maps to NM_153834.3 A443A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DS-01A-11D-A19J-08 chr17:7829387 G>A maps to NM_004732.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DS-01A-11D-A19J-08 chr3:121415619 G>A maps to ENST00000393667 D1250D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DT-01A-11D-A19J-08 chr17:15973809 T>A maps to ENST00000395857 S1410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DT-01A-11D-A19J-08 chr11:1907969 C>T maps to ENST00000381758 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DU-01A-11D-A19J-08 chr2:233710456 G>A maps to ENST00000373566 V1129V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DU-01A-11D-A19J-08 chr3:156009857 G>T maps to NM_172159.3 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DU-01A-11D-A19J-08 chr1:65117913 G>A maps to ENST00000371073 V487V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DU-01A-11D-A19J-08 chrX:103042821 C>T maps to NM_000533.3 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DU-01A-11D-A19J-08 chr7:151879573 G>A maps to ENST00000355193 Q1791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DU-01A-11D-A19J-08 chr16:2011569 C>T maps to NM_004548.2 N114N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DV-01A-12D-A202-08 chr9:125863903 A>G maps to NM_012197.3 K983K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DV-01A-12D-A202-08 chr14:39650418 T>C maps to NM_002687.3 P502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DV-01A-12D-A202-08 chr19:44515135 A>G maps to NM_006300.3 K315K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DV-01A-12D-A202-08 chr11:111625704 T>C maps to NM_181699.2 K319K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DV-01A-12D-A202-08 chr16:55363138 C>T maps to NM_024335.2 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DV-01A-12D-A202-08 chr1:207643142 G>A maps to NM_001006658.2 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DV-01A-12D-A202-08 chr10:88441197 C>T maps to NM_001171610.1 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DV-01A-12D-A202-08 chr19:36206733 T>C did not map to a codon.
Sequencing variant TCGA-ET-A3DW-01A-11D-A19J-08 chr16:72821227 T>C maps to NM_006885.3 S3649S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DW-01A-11D-A19J-08 chr1:205892513 G>A maps to NM_134325.2 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DW-01A-11D-A19J-08 chr16:30388974 C>T maps to NM_013292.3 F119F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3DW-01A-11D-A19J-08 chr11:55761603 C>T maps to NM_003697.1 L166L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A40S-01A-11D-A23M-08 chr19:334486 C>T maps to NM_017550.1 Q52Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A40S-01A-11D-A23M-08 chr16:4934539 G>A maps to NM_002705.4 A1372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A4KN-01A-11D-A257-08 chr12:62986420 C>T maps to ENST00000393630 C1683C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A4KN-01A-11D-A257-08 chr16:4563024 G>A maps to ENST00000359075 Y94Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A4KN-01A-11D-A257-08 chr15:91517939 G>A maps to NM_003981.2 R409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A22Z-01A-11D-A17V-08 chr11:65651007 T>C maps to NM_001335.3 N350N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A22Z-01A-11D-A17V-08 chr10:123970986 T>C maps to NM_206862.2 P2349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A22Z-01A-11D-A17V-08 chrX:154157147 G>A maps to NM_000132.3 P1639P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A22Z-01A-11D-A17V-08 chr17:42170140 G>A maps to NM_001015053.1 S226S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A22Z-01A-11D-A17V-08 chr17:17696274 C>T maps to ENST00000395776 R5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A22Z-01A-11D-A17V-08 chr5:37157919 T>C maps to ENST00000514429 L1669L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A22Z-01A-11D-A17V-08 chrX:40988336 G>T maps to NM_001039590.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A22Z-01A-11D-A17V-08 chrX:100383790 G>A maps to NM_006733.2 R387R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A22Z-01A-11D-A17V-08 chr10:133930582 C>T maps to NM_001105521.2 V46V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A230-01A-11D-A14W-08 chr19:12780672 C>T maps to NM_032332.3 C23C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A231-01A-11D-A14W-08 chr11:64085692 A>C maps to NM_012094.3 G2G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A231-01A-11D-A14W-08 chr22:50615509 C>T maps to NM_052839.3 F123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A231-01A-11D-A14W-08 chr17:74288473 C>T maps to NM_032134.1 Q612Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A231-01A-11D-A14W-08 chr5:178555008 G>A maps to NM_014244.4 Y856Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A231-01A-11D-A14W-08 chr20:9388616 A>G maps to NM_001172646.1 V567V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A231-01A-11D-A14W-08 chr1:178269182 G>A maps to ENST00000263528 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A231-01A-11D-A14W-08 chr14:37838729 G>A maps to NM_001195296.1 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A232-01A-11D-A14W-08 chr17:59761319 A>G maps to NM_032043.2 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A232-01A-11D-A14W-08 chr16:46843650 T>C maps to NM_001001436.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A233-01A-11D-A14W-08 chr13:102235681 C>A maps to NM_004791.1 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A233-01A-11D-A14W-08 chr6:51523916 C>T maps to NM_138694.3 S3669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A233-01A-11D-A14W-08 chr6:17765030 C>T maps to NM_022113.4 L1576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A234-01A-11D-A14W-08 chr19:38934208 C>T maps to NM_000540.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A234-01A-11D-A14W-08 chr19:33137488 T>C maps to NM_032139.2 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A235-01A-11D-A16O-08 chr2:70439916 C>T maps to NM_022173.2 G365G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A235-01A-11D-A16O-08 chr20:10025187 C>T maps to NM_198798.1 F231F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A235-01A-11D-A16O-08 chr4:68939711 G>A maps to NM_207407.2 R100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A235-01A-11D-A16O-08 chr17:48680554 G>A maps to NM_018896.3 P1388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A235-01A-11D-A16O-08 chr4:54310241 T>C maps to NM_030917.3 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A236-01A-11D-A16O-08 chr20:5903596 T>C maps to NM_001819.2 D269D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A236-01A-11D-A16O-08 chr2:96933104 C>T maps to NM_004804.2 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A237-01A-11D-A16O-08 chrX:107018376 G>A maps to NM_198057.2 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A23A-01A-11D-A17V-08 chr16:57474765 C>T maps to NM_020313.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A23A-01A-11D-A17V-08 chr19:9090830 A>G maps to NM_024690.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A23A-01A-11D-A17V-08 chr2:37088299 G>C maps to NM_003162.2 P548P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A23A-01A-11D-A17V-08 chr19:50165680 C>T did not map to a codon.
Sequencing variant TCGA-FE-A23A-01A-11D-A17V-08 chr2:60988873 A>G did not map to a codon.
Sequencing variant TCGA-FE-A3PB-01A-11D-A21Z-08 chr6:51900391 G>A maps to NM_138694.3 P1075P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PC-01A-11D-A21Z-08 chrX:48772507 A>G maps to NM_006875.3 Y128Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PC-01A-11D-A21Z-08 chr2:178378621 T>C maps to NM_003659.3 P561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PC-01A-11D-A21Z-08 chr1:201333479 G>A maps to ENST00000421663 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PC-01A-11D-A21Z-08 chr19:10930717 C>T maps to NM_001005361.2 G578G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PC-01A-11D-A21Z-08 chr19:15224521 C>T maps to NM_033025.4 A652A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PC-01A-11D-A21Z-08 chr1:93965083 T>C maps to ENST00000370253 Y28Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PC-01A-11D-A21Z-08 chr1:193038711 C>T maps to NM_004600.5 G176G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PC-01A-11D-A21Z-08 chr14:64457229 A>G maps to NM_182914.2 Q805Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PC-01A-11D-A21Z-08 chr1:28176692 C>T maps to NM_014110.4 Y264Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PD-01A-11D-A21Z-08 chr1:79095497 G>T maps to NM_006820.2 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PD-01A-11D-A21Z-08 chr16:4920916 A>G maps to NM_016936.3 K501K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PD-01A-11D-A21Z-08 chr10:24669919 T>C maps to NM_019590.3 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PD-01A-11D-A21Z-08 chr7:47921638 C>A maps to NM_138295.3 E1104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PD-01A-11D-A21Z-08 chr13:21306247 C>G maps to NM_174928.1 V80V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FE-A3PD-01A-11D-A21Z-08 chr11:94318685 G>A maps to NM_152431.2 Q237Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3S3-01A-11D-A22D-08 chr17:27024042 G>A maps to NM_003170.3 R1384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3S3-01A-11D-A22D-08 chr15:52521332 G>C maps to NM_018728.3 V1068V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3S3-01A-11D-A22D-08 chr11:67076990 G>A maps to NM_017857.3 T395T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3S3-01A-11D-A22D-08 chr19:5699183 G>A maps to NM_004793.2 S513S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3S3-01A-11D-A22D-08 chr15:69327794 C>G maps to NM_024505.3 Y319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3S3-01A-11D-A22D-08 chr5:131995904 G>A maps to NM_002188.2 E124E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3S3-01A-11D-A22D-08 chr10:27332478 C>T maps to NM_014915.2 Q679Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SB-01A-11D-A22D-08 chr22:38251637 A>G maps to ENST00000262832 P163P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SB-01A-11D-A22D-08 chr3:87017836 T>C maps to NM_016206.2 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SB-01A-11D-A22D-08 chr3:151171241 G>A maps to NM_178822.4 Y215Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SB-01A-11D-A22D-08 chr10:104416786 G>A maps to NM_030912.2 S444S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr5:140038917 G>T maps to NM_006083.3 G399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr4:69107515 G>A maps to NM_182502.3 G5G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr6:90371838 T>C maps to NM_014611.1 Q4844Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr11:18956154 G>A maps to NM_147199.3 N59N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr6:37254820 G>A maps to NM_017772.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr2:48066118 G>A maps to NM_001190274.1 Q156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr2:24964735 G>A maps to NM_003743.4 Q1129Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr17:76802344 G>A maps to NM_025090.3 T703T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr11:75442249 T>C maps to NM_025098.2 Y308Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr16:28620146 C>T maps to NM_177529.1 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr19:35757280 A>T maps to NM_205834.2 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SD-01A-11D-A22D-08 chr2:170367184 A>C maps to NM_006063.2 G299G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SE-01A-11D-A22D-08 chr12:53819000 G>C maps to NM_020547.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SE-01A-11D-A22D-08 chr17:73498979 G>A maps to NM_020753.3 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SE-01A-11D-A22D-08 chr16:67986271 C>T maps to NM_005072.4 S244S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SE-01A-11D-A22D-08 chr5:132334493 G>A maps to ENST00000509437 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SG-01A-11D-A22D-08 chr11:60777116 C>T maps to NM_006725.3 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SG-01A-11D-A22D-08 chr1:78383723 G>A did not map to a codon.
Sequencing variant TCGA-FK-A3SG-01A-11D-A22D-08 chr19:58966763 G>C maps to NM_207395.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SG-01A-11D-A22D-08 chr2:10560173 G>A maps to NM_002149.2 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SG-01A-11D-A22D-08 chrX:105970418 G>T maps to NM_194463.1 A92A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SG-01A-11D-A22D-08 chr5:70858314 C>T maps to NM_018429.2 Q2571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chr1:176993812 G>A maps to ENST00000281881 T392T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chrX:129148838 G>A maps to ENST00000303743 G697G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chr11:119244100 G>A maps to NM_004205.4 Y30Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chr5:140188523 G>A maps to NM_018907.2 S584S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chr4:146059040 A>G maps to ENST00000447906 H962H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chr10:43606830 A>G maps to NM_020975.4 E480E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chr13:51915274 C>T maps to NM_001101320.1 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chr10:50723849 G>A maps to ENST00000515869 Y905Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chr1:196715004 C>T maps to NM_000186.3 F1123F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chrX:100630266 G>A maps to NM_000061.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chr15:85461765 C>T maps to NM_004213.3 I269I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chr12:53700516 G>A maps to NM_021640.3 K273K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FK-A3SH-01A-11D-A22D-08 chr2:132021598 C>T maps to NM_001083538.1 D857D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A2QD-01A-11D-A19J-08 chr6:36475298 G>A maps to NM_007271.2 N250N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A2QD-01A-11D-A19J-08 chrX:103498971 C>T maps to NM_153448.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3BL-01A-11D-A19J-08 chr6:42713802 G>A maps to NM_003192.2 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I4-01A-11D-A21A-08 chrX:128649759 C>G maps to NM_003069.3 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I4-01A-11D-A21A-08 chr7:64853812 A>G maps to NM_152626.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I4-01A-11D-A21A-08 chr4:3443796 C>G maps to ENST00000511533 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I4-01A-11D-A21A-08 chr17:38318283 G>A maps to NM_007359.4 V162V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I5-01B-11D-A21Z-08 chr11:65636029 G>A maps to NM_016938.3 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I5-01B-11D-A21Z-08 chr20:35125294 G>A maps to ENST00000339266 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I5-01B-11D-A21Z-08 chr9:101597557 T>C maps to NM_024642.3 F315F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I5-01B-11D-A21Z-08 chr17:41141501 G>T maps to NM_173079.2 E268*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I5-01B-11D-A21Z-08 chr3:119305411 A>G maps to NM_001125.2 K193K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I5-01B-11D-A21Z-08 chr8:49643960 G>A maps to NM_024593.3 R54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I5-01B-11D-A21Z-08 chrX:71864257 G>A maps to ENST00000373539 I471I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3I5-01B-11D-A21Z-08 chr22:38951409 A>G maps to NM_007068.2 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NM-01A-11D-A21A-08 chr20:1532406 G>T maps to ENST00000381621 C117*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NM-01A-11D-A21A-08 chr9:17236414 G>A maps to NM_017738.2 K226K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NM-01A-11D-A21A-08 chr1:214820610 G>A maps to NM_016343.3 E2566E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NM-01A-11D-A21A-08 chr15:65739245 A>C maps to NM_197960.2 R891R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NM-01A-11D-A21A-08 chr12:58016596 G>T maps to NM_133489.2 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NN-01A-11D-A21A-08 chr11:69625426 G>A maps to NM_005247.2 H122H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NN-01A-11D-A21A-08 chr7:51111288 C>T maps to ENST00000395542 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NN-01A-11D-A21A-08 chr19:21606564 A>G maps to NM_001076678.2 K368K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NN-01A-11D-A21A-08 chr3:52266069 G>A maps to NM_007284.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NN-01A-11D-A21A-08 chr1:29586030 C>A maps to NM_005704.4 C210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NN-01A-11D-A21A-08 chr14:81743302 G>A maps to NM_033104.2 Y784Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NN-01A-11D-A21A-08 chr3:52402840 G>A maps to ENST00000273600 P1950P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NP-01A-11D-A21A-08 chr2:163302757 G>A maps to NM_033272.2 R442*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3NP-01A-11D-A21A-08 chr19:14267929 G>A maps to NM_001008701.2 L930L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3ON-01A-11D-A21Z-08 chr10:104353428 C>T maps to NM_016169.3 Q212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R6-01A-11D-A21Z-08 chr12:8988134 G>A maps to NM_144670.3 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R6-01A-11D-A21Z-08 chr3:52326847 G>C maps to NM_145262.3 L426L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R6-01A-11D-A21Z-08 chr21:48069638 G>A maps to NM_206962.1 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R6-01A-11D-A21Z-08 chr1:20141105 G>A maps to NM_019062.1 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R6-01A-11D-A21Z-08 chr5:150925515 C>T maps to NM_001447.2 S1724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R6-01A-11D-A21Z-08 chr21:46021267 T>G maps to ENST00000380102 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R6-01A-11D-A21Z-08 chr7:73609164 T>C maps to NM_022170.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R7-01A-11D-A21Z-08 chr2:70402826 A>C maps to NM_017880.1 V339V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R7-01A-11D-A21Z-08 chrX:9841717 G>A maps to NM_001649.2 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R7-01A-11D-A21Z-08 chr8:42259488 C>T maps to ENST00000417062 F170F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R7-01A-11D-A21Z-08 chr6:74073505 C>T maps to NM_001017361.2 R193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R7-01A-11D-A21Z-08 chr19:52869878 C>A maps to NM_001161425.1 T416T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R7-01A-11D-A21Z-08 chr12:125459963 C>T did not map to a codon.
Sequencing variant TCGA-FY-A3R8-01A-11D-A21Z-08 chr4:47644046 C>A maps to NM_006587.2 V696V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R8-01A-11D-A21Z-08 chr11:27390292 G>A maps to NM_018490.2 L659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R8-01A-11D-A21Z-08 chr6:84799014 C>T maps to NM_138409.2 Q145*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R8-01A-11D-A21Z-08 chr21:31654785 A>G maps to NM_001085455.1 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R8-01A-11D-A21Z-08 chr1:9117664 G>C maps to NM_003039.2 L45L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R8-01A-11D-A21Z-08 chr8:139662000 A>G maps to NM_152888.1 P1118P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R9-01A-11D-A21Z-08 chr4:25125831 C>A maps to NM_016955.3 G409G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R9-01A-11D-A21Z-08 chr1:237791320 G>A maps to NM_001035.2 R2127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R9-01A-11D-A21Z-08 chr6:33423521 G>A maps to NM_152735.3 E215E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R9-01A-11D-A21Z-08 chr19:52023340 T>A maps to NM_001245.5 K453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R9-01A-11D-A21Z-08 chr1:186359874 A>G maps to NM_017847.5 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R9-01A-11D-A21Z-08 chr5:140553585 C>T maps to NM_018940.2 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R9-01A-11D-A21Z-08 chr14:69707774 G>C maps to NM_001193363.1 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R9-01A-11D-A21Z-08 chr20:17445951 C>G did not map to a codon.
Sequencing variant TCGA-FY-A3R9-01A-11D-A21Z-08 chr8:113267519 T>A maps to NM_198123.1 A3333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R9-01A-11D-A21Z-08 chr13:75930350 G>T maps to ENST00000431480 R403R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3R9-01A-11D-A21Z-08 chr5:140778383 C>T maps to NM_018925.2 I230I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3RA-01A-11D-A21Z-08 chrX:63445421 G>A maps to NM_130388.2 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3W9-01A-11D-A22D-08 chr1:240071605 C>A maps to NM_000740.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3W9-01A-11D-A22D-08 chr1:223441913 G>A maps to NM_017982.3 Y155Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3W9-01A-11D-A22D-08 chr17:74383471 A>G maps to NM_182965.2 V406V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3W9-01A-11D-A22D-08 chr2:98999895 G>A maps to NM_001298.2 T147T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3W9-01A-11D-A22D-08 chr20:17639351 C>A maps to ENST00000377813 E601*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3W9-01A-11D-A22D-08 chr5:55088549 A>T maps to NM_024415.2 K462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3W9-01A-11D-A22D-08 chr10:135098941 C>T did not map to a codon.
Sequencing variant TCGA-FY-A3W9-01A-11D-A22D-08 chr4:85639708 G>A maps to NM_014991.4 Y2540Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A3WA-01A-11D-A22D-08 chr10:30915130 G>A maps to NM_183058.2 D113D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A40K-01A-11D-A23M-08 chr18:67872888 G>A maps to NM_173630.3 V2V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A4B3-01A-11D-A23U-08 chr9:135763730 C>T maps to ENST00000372136 Y134Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A4B3-01A-11D-A23U-08 chr9:139581701 C>A maps to NM_006412.3 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-FY-A4B3-01A-11D-A23U-08 chr5:5237085 G>A maps to NM_139056.2 Q676Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GE-A2C6-01A-11D-A17V-08 chr6:42236551 C>T maps to NM_033502.2 Q259Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GE-A2C6-01A-11D-A17V-08 chr11:63487680 T>C maps to ENST00000377819 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A26U-01A-11D-A16O-08 chr11:55861325 A>G maps to NM_001003750.1 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A26U-01A-11D-A16O-08 chr7:101847717 G>A maps to ENST00000360264 P996P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A2K9-01A-11D-A17V-08 chr9:90296351 C>T maps to NM_004938.2 R679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A2K9-01A-11D-A17V-08 chr11:65780826 C>T maps to NM_001323.2 Q136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A2K9-01A-11D-A17V-08 chr9:100973002 G>A maps to NM_018421.3 V536V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A2K9-01A-11D-A17V-08 chr22:46653015 A>C maps to NM_006071.1 Y2068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A3RH-01A-11D-A21Z-08 chr7:2613073 C>A maps to NM_152558.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A3RH-01A-11D-A21Z-08 chr11:128680729 T>C maps to NM_002017.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A3RH-01A-11D-A21Z-08 chr7:128359073 T>A maps to NM_032599.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A3RI-01A-11D-A21Z-08 chr2:201485428 G>C maps to NM_001159.3 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A3RI-01A-11D-A21Z-08 chr19:42848948 C>T maps to ENST00000251268 T687T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A3RI-01A-11D-A21Z-08 chr19:52537329 A>G maps to NM_014650.2 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A3RI-01A-11D-A21Z-08 chr20:49508574 A>G maps to NM_181442.1 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A3RI-01A-11D-A21Z-08 chr10:121658137 T>C maps to NM_007190.2 P121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A421-01A-11D-A23M-08 chr17:11872642 G>A maps to NM_001372.3 L4420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A421-01A-11D-A23M-08 chr12:21970199 G>A maps to NM_005691.2 D1271D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A421-01A-11D-A23M-08 chr11:67219490 G>A maps to NM_206997.1 F235F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A421-01A-11D-A23M-08 chr3:148889913 C>T maps to NM_032383.3 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A421-01A-11D-A23M-08 chr16:11217708 C>T maps to ENST00000409790 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A421-01A-11D-A23M-08 chrX:140996441 A>G maps to NM_005462.4 V1084V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A421-01A-11D-A23M-08 chr5:79354579 C>T maps to NM_003248.4 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-H2-A421-01A-11D-A23M-08 chr3:66434550 C>T maps to NM_015541.2 E645E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3EB-01A-11D-A202-08 chr1:249211397 C>A maps to NM_170725.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3EB-01A-11D-A202-08 chr19:15166254 C>T maps to NM_012114.2 R179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3EB-01A-11D-A202-08 chr9:125563189 C>A maps to NM_080859.1 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3EB-01A-11D-A202-08 chr6:114379017 A>G maps to NM_153612.3 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3EB-01A-11D-A202-08 chr4:79525502 C>A maps to NM_005139.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3EB-01A-11D-A202-08 chr6:129588336 C>A maps to NM_000426.3 S765S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3EB-01A-11D-A202-08 chr7:66410129 G>T maps to NM_017994.4 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3ED-01A-11D-A202-08 chr12:117402519 G>A maps to NM_153348.2 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3ED-01A-11D-A202-08 chr7:142565402 G>C maps to NM_004445.3 V596V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3ED-01A-11D-A202-08 chr9:140953610 C>T maps to ENST00000277549 C1519C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3ED-01A-11D-A202-08 chr19:15289708 T>A maps to NM_000435.2 P1254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3ED-01A-11D-A202-08 chr6:97561918 G>A maps to NM_052904.3 G296G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3ED-01A-11D-A202-08 chr10:61835631 C>T maps to NM_020987.2 P1669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3ED-01A-11D-A202-08 chr11:60694814 C>A maps to NM_017870.3 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr16:332687 G>A maps to NM_001176.3 E184E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr22:50315380 C>T maps to NM_001135101.1 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr11:19955322 G>A maps to ENST00000396087 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr6:160679690 G>A maps to NM_003058.3 F33F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chrX:55650392 C>T maps to NM_198451.3 D83D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr12:71978312 G>A maps to NM_003667.2 W841*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr17:34842566 C>T maps to NM_004773.2 T8T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr1:145588734 G>A did not map to a codon.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr9:100364972 G>A maps to NM_139246.4 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr19:47281987 G>A maps to NM_005628.2 Y334Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr20:44432017 G>A did not map to a codon.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr16:69726421 G>A maps to NM_138713.2 Q898Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr19:36045883 G>A maps to NM_000704.2 V807V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr19:9065419 T>G maps to NM_024690.2 T7342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr19:8842268 G>A maps to NM_001004699.1 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr1:152275907 C>T maps to NM_002016.1 Q3818Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr2:227945176 T>C maps to ENST00000396625 K595K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr15:66782755 T>C did not map to a codon.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr1:8074412 T>A maps to NM_018948.3 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr20:3675021 G>A maps to NM_023068.3 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U2-01A-21D-A22D-08 chr19:10369174 G>A maps to NM_146387.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U3-01A-11D-A22D-08 chr11:125476245 C>T maps to NM_152713.3 H222H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U3-01A-11D-A22D-08 chr10:61835973 C>T maps to NM_020987.2 A1555A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U3-01A-11D-A22D-08 chr3:113377558 T>C maps to NM_001009899.2 S990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U3-01A-11D-A22D-08 chr3:108405389 A>G maps to NM_014648.3 R1036R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U3-01A-11D-A22D-08 chr1:12387911 G>A did not map to a codon.
Sequencing variant TCGA-IM-A3U3-01A-11D-A22D-08 chr3:105464771 G>T maps to NM_170662.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IM-A3U3-01A-11D-A22D-08 chr5:140249716 C>T maps to NM_018902.3 N343N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3NZ-01A-11D-A21A-08 chr15:75134761 C>G did not map to a codon.
Sequencing variant TCGA-J8-A3NZ-01A-11D-A21A-08 chr19:45317502 G>A maps to NM_005581.3 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3NZ-01A-11D-A21A-08 chr3:127379383 G>A maps to NM_015720.2 E171E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3NZ-01A-11D-A21A-08 chr3:127779460 C>A maps to ENST00000464451 I197I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3NZ-01A-11D-A21A-08 chr19:10431411 G>A maps to NM_133452.2 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3NZ-01A-11D-A21A-08 chr3:137484264 G>A maps to NM_004189.2 Q213Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3NZ-01A-11D-A21A-08 chr1:35260770 C>G maps to NM_002060.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3NZ-01A-11D-A21A-08 chr3:119462866 C>T maps to NM_033364.3 L576L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3O0-01A-11D-A21A-08 chr16:21726415 C>T maps to ENST00000286149 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3O0-01A-11D-A21A-08 chrX:118724001 G>A maps to NM_001173487.1 N477N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3O0-01A-11D-A21A-08 chr16:58549786 G>A maps to NM_001160305.1 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3O0-01A-11D-A21A-08 chr15:72640387 C>T did not map to a codon.
Sequencing variant TCGA-J8-A3O0-01A-11D-A21A-08 chr4:81952593 G>A maps to NM_001201.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3O1-01A-11D-A21A-08 chr2:219886586 G>A maps to NM_194302.2 V1015V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A3YE-01A-12D-A23M-08 chr9:5720734 T>C maps to ENST00000414202 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A4HW-01A-11D-A257-08 chr2:191926495 C>T maps to NM_003151.2 P331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A4HW-01A-11D-A257-08 chr6:26056143 A>G maps to NM_005319.3 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A4HW-01A-11D-A257-08 chr10:12228269 C>T maps to ENST00000378937 T7T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J8-A4HW-01A-11D-A257-08 chr12:113425105 C>T maps to NM_016817.2 N147N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KS-A41J-01A-11D-A23M-08 chr16:818803 C>T did not map to a codon.
Sequencing variant TCGA-KS-A41J-01A-11D-A23M-08 chr2:71187159 C>T maps to NM_001692.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KS-A41J-01A-11D-A23M-08 chr22:45244818 C>T maps to ENST00000352766 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KS-A41J-01A-11D-A23M-08 chr22:50686832 C>T maps to NM_032019.5 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KS-A4I5-01A-11D-A257-08 chr8:13251079 T>G maps to NM_182643.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KS-A4I5-01A-11D-A257-08 chr5:140725486 G>A maps to NM_018916.3 A629A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KS-A4I5-01A-11D-A257-08 chr17:17380299 G>A did not map to a codon.
Sequencing variant TCGA-KS-A4I5-01A-11D-A257-08 chr6:7231361 C>T maps to NM_001003699.3 G1010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KS-A4I5-01A-11D-A257-08 chr8:139668160 C>T maps to NM_152888.1 G1104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KS-A4IB-01A-11D-A257-08 chr15:71300715 A>G did not map to a codon.
Sequencing variant TCGA-KS-A4IB-01A-11D-A257-08 chr10:18840834 C>A maps to NM_182543.2 G330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KS-A4IB-01A-11D-A257-08 chr10:43601915 C>T maps to NM_020975.4 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KS-A4IB-01A-11D-A257-08 chr3:49691755 C>G maps to NM_003458.3 P1589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EP-01A-11D-A257-08 chr2:71206349 G>A maps to NM_001115116.1 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4ET-01A-11D-A257-08 chr18:2728542 A>G maps to NM_015295.2 L954L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4ET-01A-11D-A257-08 chr16:3019764 G>A maps to NM_152341.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4ET-01A-11D-A257-08 chr2:143790820 T>G maps to NM_003937.2 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr8:125072865 C>T maps to NM_001039112.2 C1021C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr5:52097425 G>T maps to NM_015946.4 E304*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr10:13708198 G>A maps to NM_018027.3 L501L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr16:19711770 C>T maps to NM_020314.5 L1044L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr12:72057030 A>C maps to NM_144982.4 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr5:40854170 C>T maps to NM_032587.3 Q913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chrX:118708872 G>A maps to NM_003336.2 E18E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chrX:107834384 T>G maps to ENST00000328300 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr10:13541898 G>C maps to ENST00000396900 L109L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr17:57642991 C>T did not map to a codon.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr16:4557904 G>A maps to NM_001127205.1 Q132Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr16:72821419 A>C maps to NM_006885.3 S3585S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr7:130027836 G>C maps to NM_001868.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr19:40947969 C>T maps to NM_203344.2 K6K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr13:43462493 G>A maps to NM_001002264.1 V375V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr5:121413254 C>T maps to NM_002317.5 A142A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-L6-A4EU-01A-11D-A257-08 chr3:49933540 C>T did not map to a codon.
Sequencing variant TCGA-MK-A4N6-01A-11D-A257-08 chr3:9101881 C>T did not map to a codon.
Sequencing variant TCGA-MK-A4N6-01A-11D-A257-08 chr11:85375046 C>T maps to NM_001039618.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MK-A4N6-01A-11D-A257-08 chrX:48631754 A>G maps to NM_001080489.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MK-A4N6-01A-11D-A257-08 chr8:22054269 A>T maps to NM_006129.4 K615*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MK-A4N6-01A-11D-A257-08 chr22:45210581 G>A maps to ENST00000352766 V320V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MK-A4N7-01A-11D-A257-08 chr11:118951864 C>G maps to NM_021729.4 V833V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MK-A4N7-01A-11D-A257-08 chr2:210559315 G>T maps to NM_002374.3 E808*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MK-A4N7-01A-11D-A257-08 chr8:23167320 G>A maps to NM_002318.2 L580L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MK-A4N7-01A-11D-A257-08 chr9:4662752 G>C maps to NM_203453.2 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MK-A4N7-01A-11D-A257-08 chrX:53575048 G>A maps to ENST00000276009 S3409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MK-A4N9-01A-11D-A257-08 chr5:135389734 G>A maps to NM_000358.2 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DJ-A4UT-01A-11D-A257-08 chr1:109560185 G>A maps to NM_001142550.1 Q66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EL-A3D4-01A-11D-A19J-08 chr17:18483592 C>T did not map to a codon.
Sequencing variant TCGA-EM-A3O6-01A-11D-A21Z-08 chr6:31996292 C>A maps to ENST00000425700 R1072R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A2MY-01A-11D-A18F-08 chr1:179077162 G>C maps to NM_007314.3 S1080*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-ET-A3BV-01A-11D-A19J-08 chr1:201183350 G>A maps to NM_001164586.1 Q2925Q. Only missense variants will be evaluated by CHASM.
