5894 NP_109597 P328A not found in SNVbox database
7767 NP_001070868 T757N not found in SNVbox database
8666 NP_705833 S609I not found in SNVbox database
1134 NP_705833 V890L not found in SNVbox database
1218 NP_705833 P748R not found in SNVbox database
2356 NP_705833 Q147H not found in SNVbox database
2810 NP_705833 G696V not found in SNVbox database
3415 NP_001070868 I527S not found in SNVbox database
4339 NP_001070868 L265I not found in SNVbox database
4458 NP_001070868 G341R not found in SNVbox database
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr1:241875145 T>C maps to NM_144625.4 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr10:55617002 C>A maps to NM_001142763.1 L1251L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr12:57828749 A>C maps to NM_005538.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr15:25959388 C>G did not map to a codon.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr17:79094951 A>T maps to NM_001080395.2 S928S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr2:24991158 C>T maps to NM_003743.4 L1409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr2:139308571 A>G maps to NM_001001664.2 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr20:49367022 T>C maps to NM_032521.2 *373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr20:62648173 T>C maps to NM_012469.3 H541H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr22:29445638 C>A maps to NM_032173.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr3:38159472 A>G maps to NM_007335.2 S1554S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr3:142841233 C>A maps to NM_004267.3 R526R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr4:3441323 T>C maps to NM_198229.2 P1419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr4:78082687 C>T maps to NM_004354.2 R195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr4:140811125 C>T maps to ENST00000509479 Q488Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr5:180687082 G>T maps to NM_032765.2 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr7:15725808 G>A maps to NM_005924.4 H73H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr7:103234872 G>C maps to ENST00000428762 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr8:110131437 G>A maps to NM_003301.4 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chr9:101980773 G>A maps to NM_033087.3 I231I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7286-01A-11D-2136-08 chrX:69243091 G>C did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:100327976 C>G maps to ENST00000311030 S154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:150415710 T>C maps to NM_015203.3 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:156843560 C>T maps to NM_002529.3 F329F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr12:54764719 T>C maps to NM_001130967.1 Q275Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr12:76424936 T>C maps to NM_007350.3 Q195Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr16:1823209 G>T did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr17:40717243 G>T did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr17:44101443 C>G maps to NM_001123066.3 V746V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr2:85828226 G>T maps to NM_001031738.2 S39S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr2:179517654 G>A did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr2:179522261 C>T did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr20:1615979 C>A maps to NM_018556.3 A338A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr21:47571510 G>T maps to ENST00000397748 I199I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr3:167170763 G>A maps to NM_006217.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr4:120486566 T>C did not map to a codon.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:26104204 C>G maps to NM_003542.3 G10G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:41658861 G>A maps to ENST00000343317 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:76660532 G>A maps to NM_001563.2 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:76660635 G>A maps to NM_001563.2 I489I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr6:112454682 G>C maps to NM_001105206.1 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr8:9912061 C>T maps to NM_012331.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chrX:48321295 G>T maps to NM_033518.2 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chrX:123197833 C>A maps to NM_001042750.1 S653*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr1:63119665 T>C maps to ENST00000371140 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr1:203274778 C>T maps to NM_006763.2 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:26725401 A>G maps to NM_178498.3 H206H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:47605942 G>A maps to NM_004551.2 L235L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr11:129724697 A>G maps to NM_138788.3 A124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:6649693 A>G maps to NM_001193457.1 A557A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:11139401 C>A maps to NM_176890.2 G20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:46285792 G>A did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:53685604 A>G maps to NM_012291.4 T1884T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:113909128 A>G did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr13:37539813 C>T maps to NM_013338.4 W224*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr15:43299482 C>A did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr15:90634782 A>G did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr17:1400004 G>C maps to NM_016532.3 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:1468066 C>T maps to NM_005883.2 P1589P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:53643806 A>G maps to NM_001172674.1 I759I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:53644103 G>C maps to NM_001172674.1 G660G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr19:53644115 A>G maps to NM_001172674.1 C656C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr2:74458395 C>A maps to NM_021196.3 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr2:198001336 C>A maps to NM_001195144.1 R80R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr20:25201970 T>A maps to ENST00000443525 G349G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr22:47507401 A>G did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:53376260 G>T maps to ENST00000480258 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:145803002 A>T maps to NM_182943.2 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr3:185191374 G>A maps to NM_004721.3 G752G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr5:1064224 C>G maps to NM_006598.2 L860L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr6:111312971 G>T maps to NM_032194.1 E73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr7:72416769 G>A maps to ENST00000434423 K1249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr7:82784462 C>T maps to NM_033026.5 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr7:148702374 C>T maps to NM_004911.4 G460G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:12294415 C>A maps to NM_015378.2 L31L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:12418530 G>T maps to NM_015378.2 G3339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:26368245 C>A maps to NM_001004434.1 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:26873705 G>T maps to NM_001006665.1 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:32207654 C>A maps to NM_001703.2 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:33797901 G>T maps to ENST00000419414 S622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:36564441 C>A maps to NM_005202.2 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:38463461 G>T maps to NM_004468.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:41107429 G>T maps to NM_014747.2 I56I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:44877781 C>A maps to ENST00000453887 R5R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:45485819 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:45516767 G>T maps to NM_020883.1 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:47571881 C>A maps to NM_178134.2 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:70771958 G>T maps to NM_030816.4 R242R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:78481778 G>T maps to NM_007034.3 G288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:86890014 C>T maps to NM_006536.5 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:90398641 G>T maps to NM_001134479.1 A5A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:110032734 C>A maps to NM_153340.4 P407P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:113662125 C>A maps to NM_014813.1 P984P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:114226621 G>T maps to NM_001142782.1 E1478*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:114253016 C>A maps to NM_006608.2 S376S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:120484161 C>A maps to NM_024408.2 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:145560239 G>T maps to NM_144698.3 L242L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:153346987 G>T maps to NM_005621.1 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:153636545 G>T maps to NM_004515.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:154479795 G>T maps to NM_001098475.1 G28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:159846539 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:165652239 C>A maps to NM_000696.3 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:169510883 G>T maps to ENST00000367796 S1153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:176132950 G>T maps to NM_022457.5 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:180913532 C>A maps to NM_020950.1 P1056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:193051690 G>T did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:197021796 C>A maps to NM_001994.2 G508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:197890635 G>T maps to NM_020204.2 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:201047026 C>A maps to NM_000069.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:205272805 G>T maps to ENST00000441520 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:208207858 G>T maps to NM_025179.3 R1615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:208315681 C>A maps to NM_025179.3 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:209953827 C>A maps to NM_025228.2 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:212583856 C>A maps to NM_001198862.1 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:228459863 C>A maps to ENST00000359599 A487A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:231337237 G>T maps to NM_001004342.3 L503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:235840463 C>A maps to NM_000081.2 A3655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:235944305 G>T maps to NM_000081.2 P1691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:236195905 C>A maps to NM_002508.2 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:243652397 G>T maps to NM_006642.3 E690*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr10:43606776 G>T maps to NM_020975.4 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr10:45938568 C>A maps to NM_000698.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr10:46028620 G>T maps to NM_145021.4 S13S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr10:52103384 C>A maps to ENST00000361543 E170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr10:61832367 G>T maps to NM_020987.2 P2757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr10:75564621 G>T maps to NM_003635.3 P584P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr10:94834783 C>A maps to NM_000783.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr10:99212231 C>A maps to NM_198046.1 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr10:121196329 C>A maps to NM_005308.2 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr10:135342118 C>A maps to NM_000773.3 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:4389300 G>T maps to NM_001005161.3 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:47843668 G>T maps to NM_015231.1 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:57559043 G>T maps to NM_001085458.1 E32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:58980269 C>A maps to NM_001039396.1 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:60183163 C>A maps to NM_032597.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:60184081 C>A maps to NM_032597.3 S547S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:62343437 G>T maps to NM_022830.2 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:64676839 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:65380921 C>A maps to NM_002419.3 R102R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:66802215 G>T maps to NM_001177880.1 S45S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A4-7583-01A-11D-2136-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:67186993 C>A maps to NM_001166222.1 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:68178981 G>T maps to NM_002335.2 L799L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:71712325 C>A maps to NM_001145057.1 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:77602472 C>A maps to NM_033547.3 A828A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:94113821 G>T maps to NM_016540.3 I255I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:118390354 G>T maps to NM_001197104.1 L3723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:118869165 C>T maps to NM_198489.1 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:118900022 C>A maps to NM_001164278.1 G19G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:118919908 C>A maps to NM_001130991.1 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr11:119548417 C>A maps to NM_002855.4 E194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:6675458 G>T maps to ENST00000382421 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:44782068 G>T maps to NM_032256.1 G387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:50048001 G>T maps to NM_175736.4 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:53605575 C>A maps to NM_000966.4 E417*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:56088720 C>A maps to ENST00000347027 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:57499252 G>T maps to NM_003153.4 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:66826334 G>T maps to ENST00000359742 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:91365656 C>A maps to NM_004950.4 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:99447078 G>T maps to NM_152788.3 P878P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:112183961 T>C maps to NM_001136538.1 A741A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:118474291 G>T maps to ENST00000441406 S245S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr12:120947858 G>T maps to NM_032314.3 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr13:30091328 C>A maps to NM_003045.4 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr13:30091361 G>T maps to NM_003045.4 L532L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr13:77750688 C>A maps to NM_015057.4 T1805T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:20851385 C>A maps to NM_007110.4 E1332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:23374813 C>G did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:24546093 C>A maps to NM_006032.2 S391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:24841784 C>A maps to NM_001136022.1 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:44974945 G>T maps to NM_032135.3 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:58965533 G>T maps to ENST00000354386 G1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:69358772 G>T maps to NM_001130004.1 V361V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:88652363 G>T maps to NM_138318.2 R383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:90730383 G>T did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:91356932 G>T maps to NM_004755.2 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr14:105686446 C>A maps to NM_001519.2 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr15:28483300 G>T maps to NM_004667.4 R1271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr15:31342778 C>A maps to NM_002420.4 G402*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr15:40289184 G>T maps to NM_001013703.2 L929L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr15:40303484 G>T maps to NM_001013703.2 E1233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr15:50906460 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr15:65490856 C>A maps to NM_003613.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr15:70347515 C>A maps to NM_005078.2 E487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr15:74628372 C>A maps to ENST00000398819 T952T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr15:85400765 G>T maps to NM_020778.4 E1135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr15:91482974 C>A maps to NM_018671.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:735520 G>T maps to ENST00000248142 P715P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:1808147 G>T did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:2143706 C>A maps to NM_001009944.2 V3618V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:2342156 C>A maps to NM_001089.2 E833*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-A4-7583-01A-11D-2136-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:16244568 G>T maps to NM_001171.5 L1423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:27777776 C>A maps to NM_015202.2 P1319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:29913222 C>A maps to NM_181718.3 R311R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:29997179 G>T maps to NM_016151.2 E664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:30507455 C>A maps to NM_002209.2 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:30518143 G>T maps to NM_002209.2 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:67208825 G>T maps to ENST00000432069 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:70566422 C>A maps to NM_012426.4 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:71748521 G>T maps to NM_015020.2 S59S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:83992979 G>T maps to NM_013370.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:88643960 G>T maps to ENST00000452588 E144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr16:88706443 C>A maps to NM_013278.3 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:7129606 C>A maps to NM_004422.2 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:9066263 G>T maps to NM_004822.2 E385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:27306706 C>A maps to NM_178860.4 V283V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:27909733 G>T maps to NM_001085454.1 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:29119513 C>A maps to NM_015986.3 S301S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:37342800 G>T maps to NM_000723.3 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:40726165 G>T maps to NM_016556.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:41152113 C>A maps to NM_000988.3 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:48646300 G>T maps to NM_018896.3 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:49067868 C>A maps to ENST00000376407 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:61890687 G>T maps to NM_203499.1 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:73482022 C>A maps to ENST00000375248 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:73501037 C>A maps to NM_020753.3 V349V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:73625186 C>A maps to NM_004259.5 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:77079578 G>T maps to NM_001042573.1 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr17:80885834 G>C maps to NM_005993.4 R888R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr18:3067510 C>A maps to NM_003803.3 E1603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr18:3457730 G>T maps to NM_170695.2 A333A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr18:21395183 G>T maps to ENST00000416669 G643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr18:52546673 G>T maps to NM_004163.3 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr18:55143871 C>A maps to NM_004852.2 R478R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:1056106 C>A maps to NM_019112.3 P1427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:5082415 C>A maps to NM_015015.2 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:7550852 G>T maps to NM_080662.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:10252736 G>T maps to NM_001130823.1 S1092S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:10291561 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:11685842 C>A maps to NM_001111036.1 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:12155974 C>A maps to NM_001080404.1 G128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:12430211 G>T maps to NM_145276.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:14065196 C>A maps to NM_138353.2 R60R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:15482782 C>A maps to NM_005858.2 G340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:17122567 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:18779685 C>A maps to NM_018316.1 P493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:36348050 C>A maps to NM_199180.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:38591693 C>A maps to NM_015073.1 L619L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:38869892 G>T maps to NM_002812.4 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:38876998 G>T maps to NM_152657.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:38901761 G>T maps to ENST00000405332 A616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:44351958 C>A maps to NM_181845.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:44636131 C>A maps to NM_013362.2 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:46328568 C>A maps to NM_004819.2 E784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:46388581 G>A maps to NM_015649.1 R151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:48967487 G>T maps to NM_170720.1 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:49243526 C>A maps to NM_017805.2 E5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:51330149 C>A maps to NM_017509.2 G155G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:55591185 C>A maps to NM_133180.2 P82P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:58980671 G>T maps to NM_014347.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr19:58989074 C>A maps to NM_017908.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:8873749 C>A maps to NM_020738.2 E1293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:10192597 G>T maps to NM_003597.4 P501P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:11053068 G>T maps to NM_002236.4 E173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:24087742 C>A maps to NM_017552.1 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:26707379 G>T maps to NM_194248.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:30985977 G>T maps to ENST00000295055 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:68753241 C>A maps to NM_173545.2 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:71645730 G>T did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:74274684 C>A maps to ENST00000409262 S454S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:96852635 C>A maps to NM_020151.3 L315L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:98373702 G>T maps to NM_015348.1 S1837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:101706725 G>C maps to NM_001102426.1 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:103299927 C>A maps to NM_003048.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:103299935 G>T maps to NM_003048.3 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:110343298 C>A maps to ENST00000356688 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:125555722 G>T maps to NM_130773.2 E1014*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:136511114 C>A maps to NM_014607.3 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:163279920 G>T maps to NM_033272.2 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:170937152 C>A maps to ENST00000442603 S1865S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:179411555 A>G maps to NM_133378.4 D28965D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:189901529 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:201354860 C>A maps to NM_152387.2 G415*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:203155145 T>C maps to NM_015934.3 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:220347559 C>A maps to NM_005876.4 R1874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:234668941 G>T maps to NM_000463.2 V3V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:239005501 C>A maps to NM_016510.4 S390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:241723215 C>A maps to ENST00000373308 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:241835038 C>A maps to NM_001085437.1 E126*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-A4-7583-01A-11D-2136-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr20:1435748 C>A maps to ENST00000476071 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr20:30784821 C>A maps to NM_002657.3 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr20:30816122 C>A maps to NM_015352.1 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr20:60891751 G>T maps to NM_005560.3 L2577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr21:37418116 T>C maps to NM_017438.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr21:47614575 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr21:47977653 G>T maps to ENST00000318711 T1263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr22:23627321 C>A maps to NM_004327.3 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr22:26040629 G>T maps to NM_005160.3 E88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr22:26114260 G>T maps to NM_005160.3 L568L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr22:31485821 C>A maps to ENST00000454496 A257A. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr22:43089054 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr22:43625173 C>A maps to NM_173050.2 E330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr22:46685349 C>A maps to NM_017931.2 P378P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr22:46930961 C>A maps to NM_014246.1 V702V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:9759711 G>T did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:32932924 C>A maps to NM_001039111.1 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:45977986 G>T maps to NM_024513.2 P1331P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:47049771 G>T did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:53891718 T>C did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:57582837 G>T maps to NM_001660.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:78706341 G>T maps to NM_002941.3 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:123983419 C>A maps to NM_001024660.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:124732689 G>T maps to NM_020733.1 S578*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:138763011 C>A maps to NM_001134657.1 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:171965495 C>A maps to NM_022763.3 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:183882159 C>A maps to NM_004423.3 R113R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr3:184091300 C>A maps to NM_000460.2 G100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:1806087 G>T maps to NM_000142.4 A369A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:2896451 G>T maps to NM_014189.2 G245G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:15992901 G>T maps to NM_006017.2 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:47538505 C>A maps to NM_020453.3 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:55981536 C>A maps to NM_002253.2 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:57267613 C>A maps to NM_002703.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:87705625 G>T maps to NM_080685.2 G2016G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:94751073 C>A maps to NM_005172.1 R333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:114434487 G>A maps to ENST00000515496 F314F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:140640860 C>A maps to ENST00000509479 V1011V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:146823969 G>T maps to ENST00000508784 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr4:169377260 C>A maps to NM_001012967.1 G256*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:33947426 C>A maps to NM_016180.3 T403T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:67576766 T>G maps to ENST00000396611 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:79057655 G>T maps to NM_153610.3 L3761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:111570403 G>T maps to NM_022140.3 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:134705769 G>T maps to NM_138610.2 R79R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:148695858 C>A maps to NM_152406.2 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:150914203 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:176823782 G>T maps to NM_003052.4 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:177035608 G>T maps to NM_007255.2 G237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr5:180625783 G>T maps to NM_203293.1 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:2784634 G>T maps to NM_020135.2 E574*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:25819382 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:33132084 C>A maps to NM_080680.2 E1677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:33372925 C>A maps to NM_002263.3 R352R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:44081879 C>A maps to NM_032111.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:70840102 G>T maps to NM_001858.4 L457L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:110746233 C>A maps to NM_033125.2 E526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:117859836 C>A maps to ENST00000338728 S272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:132181526 G>T maps to NM_006208.2 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:135776922 G>T maps to NM_017651.4 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:159010768 G>T maps to NM_020823.1 V286V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:4218192 C>A maps to NM_152744.3 P1691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:5355641 C>A maps to NM_001080495.2 T2269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:6080729 C>A maps to NM_014413.3 S304S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:13971322 C>G maps to NM_004956.4 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:43484483 C>A maps to NM_015052.3 P571P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:73770880 C>A maps to NM_003388.4 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:92151472 A>G maps to NM_000466.2 N72N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:105635246 C>A maps to NM_152750.4 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:120610913 C>A maps to NM_019071.2 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:122338639 G>T maps to NM_139175.1 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr7:138536988 G>T maps to NM_001164665.1 P1758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr8:17743027 G>T maps to NM_201552.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr8:30921832 G>T maps to NM_000553.4 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr8:49831547 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr8:77618650 C>A maps to NM_024721.4 T776T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr8:80942420 G>T maps to NM_014018.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr8:92382038 C>A maps to NM_134266.1 S551S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr8:133037018 C>A maps to ENST00000262283 G593G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr8:144620240 C>A maps to NM_015117.2 G432G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr8:144899872 C>A maps to NM_078480.1 V299V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr8:145111555 G>T maps to ENST00000360660 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr9:72959148 G>T maps to NM_015110.3 L829L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr9:78808175 G>T maps to NM_006200.3 G884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr9:89771610 C>A maps to NM_001001709.2 R98R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr9:95992079 G>T maps to ENST00000297954 E262*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr9:100897129 G>T maps to NM_052820.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr9:116041304 C>A maps to NM_004697.3 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr9:129642758 C>A maps to ENST00000319119 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr9:131345546 C>A maps to NM_001130438.2 A666A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr9:136270532 G>T maps to NM_153710.3 G677G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr9:140329721 G>T maps to NM_001033113.1 L410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:12817488 C>A maps to NM_001039091.2 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:41022076 G>T maps to NM_001039590.2 L644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:44383473 C>A maps to NM_173794.3 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:47074303 C>A maps to NM_153280.2 P1051P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:48664817 G>T maps to ENST00000444343 E175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:54482658 G>T maps to NM_004463.2 L612L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:55052316 G>T maps to NM_000032.4 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:70522259 G>T did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:70598119 C>A maps to ENST00000449580 S322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:85404025 G>T maps to NM_053281.3 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:100912055 G>T maps to NM_177949.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:114347864 C>A maps to NM_020871.3 E738*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:120182119 C>T maps to NM_012084.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:129059134 C>A maps to NM_006649.3 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:132351709 G>T maps to NM_016521.2 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:153928304 G>T maps to NM_001081573.1 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr1:54870253 C>T maps to NM_145716.2 W62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr1:186083138 G>A maps to NM_031935.2 Q3720Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr11:6265519 C>A maps to NM_001037329.2 R537R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr11:111749724 A>G maps to ENST00000428306 D44D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:14772232 A>C maps to NM_004963.3 A929A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:41316145 C>T maps to NM_001843.2 Q106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:78604233 C>T maps to NM_014903.4 C2343C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr12:105527568 C>G maps to NM_015275.1 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr13:45768534 G>A maps to NM_198404.2 D56D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr14:75355976 G>T did not map to a codon.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr16:50112740 G>T maps to NM_182922.2 G285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr17:28407884 G>C maps to NM_198529.3 L1104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:12768880 G>T maps to NM_000528.3 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:13996868 C>G did not map to a codon.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:35828751 C>T maps to NM_001771.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr19:55144005 C>A maps to ENST00000427581 G287G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:109109238 C>T maps to NM_181453.3 T1480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:207040929 G>A maps to NM_005279.3 L348L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:238722325 G>T did not map to a codon.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr20:44578918 G>C maps to NM_022095.3 T1142T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr21:11097540 C>A did not map to a codon.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr3:69928531 A>T maps to ENST00000448226 K118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr4:54266006 G>C did not map to a codon.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr4:155465647 T>C maps to NM_002669.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr8:132968017 C>T maps to NM_015137.3 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr9:125852574 G>T maps to NM_012197.3 E847*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:32207415 C>A maps to NM_001703.2 E524*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:46086773 G>T maps to NM_001114938.2 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:150258999 T>A maps to NM_144697.2 T264T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:162344113 T>C maps to NM_182581.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:190067268 A>T maps to NM_199051.1 L727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:198704381 G>A did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr12:53097169 G>T maps to NM_175078.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr12:120599293 C>T maps to NM_006836.1 E812E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr13:109793008 C>T maps to NM_015011.1 H1461H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr14:69866097 C>T maps to NM_018375.3 F4F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr15:65295423 A>C maps to NM_139242.3 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr15:72767219 C>A maps to NM_005744.3 G80G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr16:84158327 A>C maps to NM_031463.4 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr17:58740445 G>T maps to NM_003620.3 E451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr17:61490919 G>T maps to ENST00000389520 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr17:80115740 C>T maps to ENST00000445854 E708E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr19:17100467 G>T maps to ENST00000443236 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:99720472 C>A maps to NM_025244.2 E190*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:136736936 C>A did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:149835495 C>T maps to NM_004522.1 Q452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr2:179449123 T>C maps to NM_133378.4 E19150E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr20:50221536 C>G maps to NM_006045.1 A942A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr21:38534336 G>T maps to NM_003316.3 E1048*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr22:26423001 C>G maps to ENST00000407587 L2356L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr3:9512541 T>C maps to ENST00000407969 L1061L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr4:123156096 G>T maps to NM_015312.3 E1165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr5:7867620 A>G maps to NM_024091.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr5:176696647 C>T maps to NM_022455.4 N1783N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr6:8413925 T>C maps to NM_001142540.1 V354V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr7:30893076 T>C did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr7:36396612 G>A maps to NM_001100425.1 F255F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr7:138602634 C>T maps to NM_001164665.1 P579P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr9:129595384 G>T maps to NM_014007.3 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr9:137734001 G>C did not map to a codon.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:46497073 C>A maps to NM_015112.2 R1002R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:94548961 G>A maps to NM_000350.2 I268I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:114402064 A>G maps to NM_015967.5 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr1:213244384 T>C did not map to a codon.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr11:14510131 T>C did not map to a codon.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr11:118969111 C>T did not map to a codon.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr14:102910131 G>A maps to NM_014844.3 P967P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr19:1881549 G>A maps to NM_031213.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr2:61454344 A>C maps to NM_014709.3 V2484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr6:31779707 G>A maps to NM_005527.3 G14G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr7:103029856 G>A maps to ENST00000354356 A442A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr7:131241088 C>T maps to NM_001018111.2 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr8:22368689 C>A maps to ENST00000397775 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr8:144801160 A>T did not map to a codon.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr9:32988091 T>A maps to NM_001195248.1 K71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:70819791 G>T maps to NM_030816.4 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:91406115 G>A maps to NM_201269.1 F265F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:109793252 C>A maps to NM_001408.2 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:112524715 C>T maps to ENST00000315987 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr1:161049404 C>T maps to NM_030916.2 Q138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr10:63852306 C>A maps to NM_032199.2 R1029R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr10:74095535 A>T did not map to a codon.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr12:49390897 C>A maps to NM_015086.1 S587S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr14:45579917 A>G maps to NM_017922.3 E490E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr15:64454354 T>C did not map to a codon.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr15:75132965 T>C maps to NM_001099436.1 Q162Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr16:1634391 C>A maps to NM_014714.3 V395V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr16:57806197 T>C maps to NM_005550.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr17:1370771 A>C did not map to a codon.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr17:79425868 G>T maps to ENST00000436173 E1827*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr19:50783388 C>T maps to NM_001145809.1 H1376H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr2:21251316 G>A maps to NM_000384.2 Q571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr2:88926546 C>A maps to NM_004836.5 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr2:114399721 G>A did not map to a codon.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr20:46386050 C>A maps to NM_001161841.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr21:43166866 G>C maps to ENST00000352483 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr3:183756413 T>A did not map to a codon.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr4:89410408 C>G maps to NM_016323.2 V685V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr4:126411929 C>A maps to NM_024582.4 I4651I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr5:132425376 T>C maps to NM_002154.3 D456D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr5:147818021 C>A maps to NM_205836.1 P995P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr6:56463336 T>C maps to ENST00000361203 A3744A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr8:63936644 G>T maps to NM_003878.2 S200S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr8:110420392 G>C maps to ENST00000426474 G643G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr9:17394560 T>C maps to NM_017738.2 S703S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr9:125582791 G>A maps to NM_005388.4 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr1:228467537 C>G maps to NM_001098623.1 L2471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr10:32854548 G>T did not map to a codon.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr11:59622264 A>G maps to NM_001062.3 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr11:120300473 C>T maps to NM_015313.2 I239I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr12:54857069 A>G maps to NM_144594.2 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr12:78574709 A>G maps to NM_014903.4 T1837T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr13:26625046 G>A maps to NM_001007538.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr16:3081003 G>A maps to NM_001103175.1 R144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr17:48734447 C>T maps to NM_003786.3 G130G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr17:56281633 G>A maps to NM_000502.4 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr19:8563523 C>A maps to NM_032152.4 E390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr19:55966663 G>A maps to NM_024710.2 Q144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr2:174231882 G>A maps to NM_031942.4 W397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr20:37623475 C>A maps to NM_021931.3 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr20:62851190 C>T maps to NM_004535.2 D699D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr5:52366068 C>G maps to NM_002203.3 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr5:128797257 G>C maps to NM_133638.3 L179L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr5:140307712 A>G maps to NM_018898.3 Q412Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr6:123022646 T>C did not map to a codon.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr7:45956266 C>A did not map to a codon.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chr9:96055158 C>T maps to ENST00000297954 P1841P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chrX:71379996 C>G maps to NM_207422.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7828-01A-11D-2136-08 chrX:152960546 C>T maps to NM_005629.3 Q596*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr1:6639490 C>T maps to NM_138697.3 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr1:39908527 C>G maps to ENST00000361689 S4357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr1:153651703 A>G maps to NM_000906.3 V40V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr1:204960429 C>A maps to ENST00000367172 T1033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr10:89501011 C>T maps to NM_001015880.1 D369D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr11:43837919 T>C maps to NM_016142.2 I160I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr11:66444484 G>A maps to NM_031492.2 F22F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr11:92917686 C>A did not map to a codon.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr14:20840923 T>C maps to NM_007110.4 K2348K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr19:4290584 C>T maps to NM_020209.3 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr19:39328276 C>A maps to ENST00000221419 L524L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr20:56137932 G>T maps to NM_002591.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr22:38877224 G>A maps to NM_016657.1 W120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr3:52678739 A>G maps to ENST00000296302 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr3:69169079 T>C maps to NM_198271.3 E142E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr7:33136130 G>A maps to NM_203288.1 D147D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7915-01A-11D-2201-08 chr7:155596097 G>A maps to NM_000193.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:55612676 A>G maps to NM_015306.2 Y725Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:152082278 C>T maps to NM_007113.2 R1138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr1:154841687 G>A maps to NM_002249.4 S251S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr10:129209145 G>A maps to ENST00000398025 R1507R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:61081865 G>A maps to NM_001923.3 A501A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:65423174 A>G maps to NM_021975.3 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr11:113295343 A>G maps to ENST00000355319 D10D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr15:89398461 C>T maps to NM_013227.3 F882F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr17:38416824 G>A maps to NM_133264.4 Q34Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr18:47800702 C>T maps to ENST00000424334 R384R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:7810713 G>A maps to NM_021155.3 I146I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:15350518 C>T maps to NM_058243.2 E1132E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:40419756 A>G maps to NM_003890.2 H1079H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr19:53762786 C>T maps to NM_173856.2 R387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:102849532 C>T maps to NM_003854.2 Q416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:149850957 G>C maps to NM_004522.1 L643L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:162227814 T>C maps to NM_005805.4 I148I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:165600385 C>A did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr2:182322979 C>A maps to NM_000885.4 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr20:19679324 G>C did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr21:46916962 G>T did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr3:48447206 T>C did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr3:113376112 C>T maps to NM_001009899.2 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr6:51930864 A>G maps to NM_138694.3 S263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr6:162864431 C>T maps to NM_004562.2 K27K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr7:103159948 T>C maps to ENST00000428762 L2561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr7:150553626 G>C maps to ENST00000416793 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr8:53570006 C>T maps to NM_014781.4 L794L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr8:67405942 T>A maps to NM_152765.3 I20I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr9:2718278 C>T maps to NM_133497.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr9:127572162 C>T maps to NM_182487.2 Y477Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:46290208 T>C maps to NM_015112.2 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:145761287 T>C maps to NM_002614.3 D367D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:209974722 G>A maps to NM_006147.2 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:226127229 G>A maps to NM_003240.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr1:234744250 G>T maps to NM_182972.2 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr10:73055665 C>T maps to NM_170744.3 L758L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr10:102732886 G>A maps to NM_017893.2 E42E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr11:2181207 G>T maps to NM_001185098.1 G69G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr11:108155201 T>C did not map to a codon.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr12:6138618 G>A maps to NM_000552.3 H952H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr12:48375151 C>A maps to NM_001844.4 G813*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr12:132405712 C>G maps to NM_003565.2 A1010A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr13:52343424 C>A maps to NM_024705.1 V188V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr14:58827677 G>T maps to NM_002892.3 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:32916474 C>T maps to NM_014783.3 L133L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:52446238 C>T maps to NM_016194.3 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:64021463 C>T maps to ENST00000261887 W1042*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr15:99672332 G>T maps to ENST00000336292 V1255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr16:1869996 A>G maps to NM_005326.4 N111N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr19:22817277 T>G did not map to a codon.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr2:54587527 G>T maps to NM_001100396.1 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr20:419912 G>T maps to ENST00000246077 V290V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr20:49219115 G>A maps to NM_080829.2 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr21:27348293 A>C maps to NM_000484.3 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr21:46930114 G>A maps to ENST00000359759 Q1626Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr3:56787576 G>C maps to NM_001128615.1 S163S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr3:184071154 C>A maps to NM_004366.4 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr8:10470572 C>T maps to NM_178857.5 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr8:39862888 T>C maps to NM_194294.2 F250F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7997-01A-11D-2201-08 chr9:16419220 A>G maps to NM_017637.5 S1022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:151109385 C>T maps to NM_001178061.1 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:167096128 A>G maps to NM_001080426.1 T587T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:169806132 C>T maps to NM_018186.2 S535S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr1:203025586 C>A maps to ENST00000367238 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr10:104415048 G>A maps to NM_030912.2 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:32676506 T>C maps to NM_001008391.2 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:82877723 A>G maps to NM_015885.3 K595K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:117077796 G>A maps to NM_004716.2 I622I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr12:54856510 T>A did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr13:25029239 T>C maps to NM_006437.3 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr14:24032847 C>T did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr14:105410342 C>A maps to NM_138420.2 V3815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr15:44090644 A>T maps to ENST00000319327 I172I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr15:101529602 A>G maps to NM_024652.3 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:570231 C>T maps to NM_014700.3 R657R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:31098020 C>T maps to NM_001039503.2 Q147Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:56485679 T>C did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr17:34077158 G>C maps to NM_139285.2 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr17:45056016 C>T maps to NM_203400.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr17:65665780 T>C did not map to a codon.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr18:11689822 G>A maps to NM_182978.2 E87E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:3730390 C>G maps to NM_014428.1 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:7615222 G>A maps to NM_001166111.1 A627A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:41018831 A>G maps to NM_020971.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr19:47259237 G>A maps to NM_024301.4 E177E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:27248499 C>T maps to NM_012326.2 G173G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:37365710 G>A maps to NM_001135651.1 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:85981695 G>T maps to NM_032827.6 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:98413328 T>A maps to NM_015348.1 A997A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:107032392 G>A maps to ENST00000304514 L1659L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr2:238280360 C>T maps to NM_057165.4 A1227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr20:4229280 A>G maps to NM_000678.3 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr20:35177591 C>T maps to NM_006097.3 N153N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr3:62499342 A>G maps to NM_183394.2 L874L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:74026106 G>T maps to NM_032380.3 I568I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:74981181 G>C maps to NM_001099271.1 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:140724209 A>T maps to NM_018916.3 K204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr5:179160184 C>T maps to NM_014757.4 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr6:43266248 G>A maps to ENST00000372585 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr9:136305498 G>T maps to NM_139025.3 G607G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chrX:57313329 A>G maps to NM_174912.3 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr1:17939551 G>T did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr1:150634374 A>T maps to ENST00000369003 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr12:6638742 C>A maps to NM_014865.3 R1213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr14:94756789 C>T maps to NM_001100607.1 E47E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr15:59515312 C>G maps to NM_004998.2 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr15:66010114 C>G did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr15:75499126 C>A maps to NM_015492.4 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr16:14755822 G>T maps to NM_016561.2 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr16:17202724 C>A maps to NM_022166.3 E903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:8350136 T>C maps to ENST00000402554 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:33749974 C>A maps to NM_018042.3 E25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:40025022 T>C maps to ENST00000401700 E1094E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:59668190 C>T maps to NM_199290.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr17:80202674 C>T maps to NM_001893.3 Q410Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr18:29054159 A>G maps to NM_001944.2 G726G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr2:95540715 G>A maps to NM_144705.2 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr2:220239738 G>A maps to NM_012100.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr20:31375211 G>A maps to NM_006892.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr4:52765462 T>C maps to ENST00000451288 N222N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr4:141590819 G>T maps to NM_015130.2 R469R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr5:39390644 A>G maps to NM_001343.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr5:39394410 T>C maps to NM_001343.2 E4E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr6:153332801 A>T maps to NM_012419.4 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr7:151945348 T>A maps to ENST00000355193 K724*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:17419588 G>A maps to NM_001164771.1 Q587Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:132052525 G>A maps to NM_001115.2 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr8:143957216 G>A maps to ENST00000377675 S415S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr9:86587098 G>T maps to NM_031262.2 P217P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr9:139272474 G>T maps to NM_003086.2 A1268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chrX:39932879 G>T maps to NM_001123385.1 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chrX:70444363 C>T maps to NM_000166.5 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr1:10678474 G>A did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr1:230372158 C>T maps to NM_004481.3 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:63273899 G>C maps to NM_001142535.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:65788965 C>T did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr11:118771982 C>T maps to NM_182557.2 Q823Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr12:52401015 C>A maps to NM_181711.2 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr15:41864762 G>A did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr16:568987 G>A maps to NM_014700.3 T562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr16:1822946 C>G maps to ENST00000432952 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:4542863 G>A maps to NM_001140.3 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:36099581 T>C maps to NM_000458.2 Q131Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:38926070 C>A maps to NM_181539.4 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr17:80443513 C>T maps to ENST00000374611 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr19:2416796 G>A maps to NM_182973.1 Q635Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr19:9077785 G>T maps to NM_024690.2 I3220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr2:45616664 G>C maps to NM_018079.4 G924G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr20:32026770 G>A maps to NM_003098.2 D124D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr21:44589373 C>G maps to NM_000394.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr21:47958480 G>A maps to ENST00000318711 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr22:20920815 G>A maps to NM_001003891.1 Q251Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr22:39138451 G>A maps to ENST00000405018 L329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr3:73673577 G>C maps to NM_015009.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:437055 A>G maps to NM_133474.2 S400S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:983982 T>C maps to NM_213613.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr4:119666216 T>A did not map to a codon.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr5:32407028 A>T maps to NM_016107.3 A294A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr5:101834203 C>A maps to NM_173488.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr5:139947278 T>A maps to NM_080670.2 A175A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr6:41129013 C>T maps to NM_018965.2 V126V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr6:80197554 C>T maps to NM_181714.3 K420K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr7:134873247 C>T maps to NM_014149.3 E606E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr8:48744422 G>T maps to NM_006904.6 L2738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chrX:15682859 A>G maps to NM_020665.4 H13H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr1:200860814 A>G maps to NM_018265.2 R49R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr1:234744214 G>A maps to NM_182972.2 N342N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr11:123448254 G>A maps to ENST00000456860 Q68Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr12:49522586 G>A maps to NM_006082.2 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr14:70527577 C>T maps to NM_183002.1 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr15:25972304 A>T did not map to a codon.
Multiple mappings detected for codon TCGA-A4-8312-01A-11D-2396-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr16:30718523 G>T maps to NM_006662.2 R109R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr17:47302351 G>T maps to NM_001143804.1 A45A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr17:48600412 A>T maps to NM_032133.4 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr2:217279801 C>G maps to NM_014140.3 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr20:57611523 A>C did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr5:150518239 G>T maps to NM_001155.4 S106*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr7:66474574 C>T maps to NM_018264.2 F93F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr7:83023611 C>G did not map to a codon.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr9:123527052 G>A maps to NM_012164.3 D383D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chrX:18972369 A>G did not map to a codon.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr1:27107194 C>A maps to NM_006015.4 S2269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr1:109649720 G>A maps to NM_001122961.1 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr10:104120010 T>C maps to NM_004193.2 N416N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr11:19954836 G>A maps to ENST00000396087 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr11:47745664 A>G maps to NM_015308.2 A793A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr12:83290129 G>A maps to NM_152588.1 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr15:66031103 A>G maps to ENST00000443035 N247N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr17:1633710 G>A maps to NM_001163809.1 K1235K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr17:10433385 G>A maps to NM_017534.5 A901A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr17:61561774 G>C maps to NM_000789.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr19:13919689 C>A maps to NM_023072.2 A251A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr2:113069432 G>A maps to NM_198581.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr20:34215309 G>T maps to NM_003915.5 Y381*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr3:12957105 C>T maps to ENST00000429247 V716V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr3:37369906 A>G maps to NM_001172713.1 K2002K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr4:164050123 T>G maps to NM_138386.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr5:131546091 G>T maps to NM_001142599.1 A198A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr6:127611394 T>C maps to NM_001139510.1 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr7:18625058 C>T maps to NM_178425.2 Q60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr7:35707132 A>G maps to NM_022373.4 G135G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chr9:35560974 G>A maps to NM_001135999.1 L1410L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8515-01A-11D-2396-08 chrX:120182119 C>T maps to NM_012084.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:31347252 G>T maps to NM_014654.3 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:52256296 C>A maps to NM_002525.2 E1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:110561172 G>A did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr1:160305058 A>G maps to NM_001098398.1 D94D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr10:61112191 C>A maps to ENST00000442566 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr10:93999657 A>C maps to NM_014912.4 T150T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr11:67787233 A>T maps to NM_001161473.1 L176L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr11:87908438 G>A maps to NM_022337.2 Y38Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr12:49334776 T>C maps to NM_001659.2 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr14:92349358 G>T maps to ENST00000267620 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr15:42462023 G>T maps to ENST00000348544 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr16:80654829 G>T maps to NM_152342.2 I279I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr16:84228708 G>A maps to NM_139174.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr19:15303026 G>T maps to NM_000435.2 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr2:27373230 A>T maps to NM_175769.2 K155*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr2:54851999 C>T maps to NM_003128.2 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr20:47628618 C>A maps to NM_006420.2 R1306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:20796431 G>C maps to NM_032775.3 A611A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:46765597 A>G maps to NM_014246.1 A2621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr22:50926722 G>T maps to NM_017584.5 G120G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr3:50357590 C>T maps to NM_033158.4 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr3:179426710 C>A maps to NM_003940.2 A257A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr4:122724129 G>A maps to NM_001034194.1 K114K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr5:140724919 G>T maps to NM_018916.3 L440L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr5:150444533 C>G maps to NM_006058.3 G41G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:44747233 T>C maps to ENST00000444676 N965N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:149502568 C>A maps to NM_198455.2 G2795G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr7:156963037 T>A maps to NM_014671.2 L79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr8:28991586 C>T maps to NM_015254.3 P918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr9:94821489 G>A maps to NM_006415.2 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chrX:108780249 G>A maps to NM_018698.3 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chrX:135960072 C>T did not map to a codon.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr1:110774915 G>A maps to NM_004978.4 L631L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr1:116226630 C>A maps to NM_001172412.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr1:209878261 G>A did not map to a codon.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr11:17542426 G>T maps to NM_153676.3 R400R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr11:17542435 T>G maps to NM_153676.3 V397V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr12:110813920 T>C maps to NM_016238.2 V520V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr12:112098448 G>C maps to NM_006768.3 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr13:26625046 G>A maps to NM_001007538.1 L23L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr15:64692968 T>C maps to NM_016213.4 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr17:48628510 C>A maps to NM_022827.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr17:80559302 C>A maps to NM_004514.3 G637G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:5220166 T>A did not map to a codon.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:10506723 G>C maps to NM_007065.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:18499105 A>G maps to NM_004864.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:45381870 T>C maps to NM_002856.2 Y478Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr19:50305817 C>T maps to NM_014203.2 S714S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr2:230910734 G>A maps to NM_152527.4 I369I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr20:40710578 G>A maps to ENST00000373198 D1427D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr21:35743146 T>C maps to NM_172201.1 *124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr3:19389245 G>A maps to NM_144633.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr3:113376112 C>T maps to NM_001009899.2 Q1472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr3:183898701 T>G maps to ENST00000411763 G190G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr4:25398291 G>C maps to ENST00000510092 S356S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr6:37139028 C>G maps to ENST00000373507 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr6:150290453 G>T maps to NM_025218.2 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chrX:150869295 C>A maps to NM_024082.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chrX:150891104 T>G maps to NM_033085.2 Y142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:1480324 C>T maps to NM_014188.2 R94R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:22310246 C>T maps to NM_007352.2 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:33985174 T>A maps to ENST00000373381 T3573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:43166451 G>A maps to NM_004559.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr1:117122272 G>A maps to NM_001542.2 D1045D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr10:112342363 A>G maps to NM_005445.3 L256L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr12:4554424 G>A maps to NM_020996.1 G104G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr12:51450185 G>A maps to ENST00000448283 L285L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr12:124887101 C>T maps to NM_006312.4 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr15:25615994 A>G maps to NM_000462.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr16:67236621 T>A maps to NM_024712.3 T550T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr16:90023965 G>A maps to NM_207514.1 E151E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr17:6703553 C>A did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr17:39305509 G>A maps to NM_033188.3 C170C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr17:65074430 G>A maps to NM_014877.3 L1922L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr18:2718193 C>T maps to NM_015295.2 Q767*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr18:52921811 A>G maps to ENST00000398339 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr19:1460856 G>T did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr19:6420476 G>C maps to NM_003685.2 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr2:27291527 A>G maps to NM_021831.5 G757G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr20:48098852 C>G maps to NM_004975.2 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr3:118945880 C>T maps to NM_212543.1 Q87Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr4:106967780 G>A maps to NM_001163436.1 G876G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr4:113578402 T>C maps to ENST00000509061 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr4:190874220 A>G did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr5:129241298 C>T maps to NM_175856.4 R259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr5:131953818 A>G maps to NM_005732.3 A1074A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr5:176471534 G>C did not map to a codon.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr6:155566797 G>A maps to ENST00000456144 A1195A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chr9:131670919 G>T maps to NM_001127244.1 E493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chrX:19026232 C>G maps to NM_001079858.2 L477L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8630-01A-11D-2396-08 chrX:20206636 T>C maps to NM_004586.2 E203E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:2426374 C>T maps to NM_014638.2 F580F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:12628410 T>C maps to NM_004753.4 S289S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:155015934 G>T maps to NM_152494.3 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr1:197069638 G>A maps to NM_018136.4 I2914I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr10:88681452 G>A did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr11:1268537 G>A maps to ENST00000447027 S3479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr12:53225245 C>A maps to NM_175834.2 G214G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr12:57389790 C>G maps to NM_007264.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr12:57965900 C>T maps to NM_004984.2 Q474*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr13:21163993 T>C maps to NM_175605.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr15:39886355 C>A maps to NM_003246.2 Y1108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr15:72190907 A>G maps to ENST00000424560 P1312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:4557883 G>T maps to NM_001127205.1 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:20559487 G>A maps to NM_182617.3 Q332*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:87764192 T>C maps to NM_017566.3 Q188Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr16:88105727 G>A maps to NM_001173543.1 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr19:36029206 A>C did not map to a codon.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr2:170012841 G>T maps to NM_004525.2 V4031V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr22:40800333 C>T maps to NM_015705.4 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:13399892 G>A maps to NM_024923.2 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:15298470 G>A maps to NM_004844.3 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:15765924 G>A maps to NM_015199.3 I219I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:38316202 T>C maps to NM_004256.3 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:42577628 C>T maps to NM_004624.3 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr3:154855892 T>A maps to NM_007289.2 A241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr4:141590873 G>A maps to NM_015130.2 L451L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr5:7867845 A>G maps to NM_024091.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr5:89971180 C>T maps to NM_032119.3 I1744I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr6:2948771 C>A maps to ENST00000316782 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr6:109690200 C>T maps to NM_006016.4 V149V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr6:158330821 T>G maps to NM_016224.3 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr7:27582615 C>G maps to NM_152740.3 V196V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr7:100344176 C>T maps to ENST00000349350 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr7:117375371 C>T maps to NM_033427.2 L1213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr8:27516083 C>T maps to NM_016240.2 Q133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr8:145947049 A>T maps to NM_138367.1 I665I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chr9:104125252 T>C maps to NM_001701.3 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A48D-01A-11D-A25F-10 chrX:107977150 G>A maps to NM_003604.2 Y808Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr12:85279277 A>G maps to NM_182767.4 S170S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr12:133359034 C>T maps to NM_005895.3 E1104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr15:41798199 G>T maps to NM_002344.5 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr16:18849888 A>G maps to ENST00000389467 N2356N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr16:90127012 C>A maps to NM_001098173.1 R323R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr17:45918191 A>G maps to NM_138355.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr21:34725062 G>A did not map to a codon.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr3:8809351 G>T maps to NM_000916.3 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr4:10099337 A>G maps to NM_017491.3 I185I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr5:353962 C>T maps to NM_020731.3 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr5:96443095 C>A maps to NM_153234.4 E119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr8:120628548 G>T maps to NM_006209.3 R245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr1:12835788 C>T maps to NM_001080830.1 R131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr1:17907126 G>T maps to NM_018125.3 G13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr1:152883241 T>G maps to NM_005547.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr10:118357346 T>C maps to NM_006229.2 D194D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr11:34378950 G>T maps to NM_145804.2 S60S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr11:48347235 C>T maps to NM_001004702.1 Y248Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr12:6645957 T>C did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr12:114841565 G>A maps to NM_000192.3 F46F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr12:122669245 T>C maps to NM_001098519.1 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr13:75923414 C>A maps to ENST00000431480 L433L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr14:20846266 G>C maps to NM_007110.4 A1879A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr15:32929466 T>C maps to NM_014783.3 L831L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr16:74716658 G>T maps to NM_152649.2 V282V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr19:1132139 G>A maps to NM_001100122.1 A19A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr2:113540316 G>T maps to NM_000575.3 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr2:201719789 T>G maps to NM_001162407.1 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr2:220072713 C>T maps to NM_138802.1 L130L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr3:32433538 G>C maps to NM_138410.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr3:138340382 T>A did not map to a codon.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr4:55570035 C>G maps to NM_000222.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:26597327 A>T maps to NM_013375.2 K40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:129766959 C>T maps to NM_000426.3 A2141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:132859484 C>T maps to NM_175057.3 N19N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr6:139235872 G>T maps to ENST00000367663 A582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:18975516 C>T maps to NM_178425.2 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:31377934 G>A maps to NM_022728.2 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:63537708 A>T maps to NM_001159522.1 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A57E-01A-11D-A26P-10 chr7:142606702 G>A maps to NM_019841.4 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr12:26348667 C>G maps to NM_005086.4 A21A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr14:21793035 C>T maps to NM_020366.3 P674P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr15:38776826 T>A maps to NM_173611.2 G423G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr15:81181039 A>T did not map to a codon.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr18:42281355 C>T maps to NM_015559.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr2:44457730 T>C maps to NM_002706.4 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr20:61050058 G>T maps to NM_080473.4 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr20:61945125 G>T maps to ENST00000326996 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr22:41911895 T>C maps to ENST00000396512 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr6:97051596 A>G maps to NM_020482.4 V36V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr7:5372498 C>T maps to NM_001080495.2 K1967K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr7:70229863 C>G maps to NM_015570.2 T447T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr8:94934632 C>T maps to NM_001161778.1 Q175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chr8:120580454 G>A maps to NM_006209.3 F749F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5DU-01A-11D-A28G-10 chrX:154299903 A>C maps to NM_024332.2 V34V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr1:2066776 C>T maps to NM_002744.4 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr1:91403568 G>T maps to NM_201269.1 S1054*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr11:95825220 C>T maps to NM_032427.1 Q658Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr11:105623881 A>T maps to NM_000829.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr12:59274492 G>A maps to NM_153377.3 G557G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr15:75132622 C>T maps to NM_001099436.1 R216R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr16:3063764 C>A maps to NM_020982.3 I134I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr19:10610565 G>T maps to NM_203500.1 G48G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr19:36229180 A>G did not map to a codon.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:33810280 T>C maps to ENST00000395190 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:71036917 G>A maps to NM_173535.2 S537S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:86947924 G>A maps to NM_022780.3 Q45Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr2:242196032 T>C maps to NM_005336.3 L213L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:48692762 T>A maps to NM_001407.2 T1602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:49689058 C>A maps to NM_003458.3 I690I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:93646099 C>T maps to NM_000313.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr3:170002333 T>C maps to NM_002740.5 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr4:169382990 C>T maps to NM_001012967.1 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr5:140800832 G>A maps to NM_018914.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr7:30492405 G>A maps to NM_006092.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr7:100279775 C>T maps to NM_022574.4 T948T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr7:100485328 T>C maps to NM_015908.5 P725P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chr8:53569321 G>A maps to NM_014781.4 Q1023*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5XZ-01A-11D-A31X-10 chrX:39932147 A>G maps to NM_001123385.1 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:9305535 C>T maps to NM_004285.3 F181F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:120506374 G>T maps to NM_024408.2 C579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:156294857 A>G maps to NM_005998.4 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr10:94828243 C>A maps to NM_183374.2 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr11:3143329 T>C did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr14:73959008 G>A maps to NM_024644.2 V429V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr17:15971430 T>G maps to ENST00000395857 T1522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr17:42335910 T>A maps to NM_000342.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr17:51901647 C>T maps to NM_032559.4 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr18:6992668 G>A maps to NM_005559.2 L1687L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr18:74700844 C>T maps to NM_001025101.1 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr2:58386911 T>C maps to NM_001114636.1 G377G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr3:137849688 A>C did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr3:179298769 G>T maps to NM_004301.3 G307*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr4:39435919 G>T maps to NM_175737.3 E306*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr6:32944713 G>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr6:44148400 T>G did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr7:157177600 T>C maps to NM_058246.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr1:224468832 G>A maps to NM_002533.2 L652L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr10:118893698 C>T maps to NM_001112704.1 L275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr10:119044854 G>A maps to NM_173791.3 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr11:2798239 C>G maps to NM_000218.2 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr11:30032893 T>C maps to NM_002233.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr11:46419221 G>A maps to ENST00000458649 G1225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr12:21680691 G>C maps to NM_030572.2 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:51368557 C>T maps to ENST00000337334 N264N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:67787026 T>C maps to NM_022474.2 L484L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr14:75248110 G>A maps to NM_019589.2 W455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:40913800 A>T maps to NM_170589.3 R473*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:62155702 C>A maps to NM_020821.2 E3630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:81517937 A>G maps to NM_172217.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr15:89856163 A>T maps to NM_001113378.1 G1227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr16:1877592 G>T maps to NM_001018104.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr16:66670439 T>A maps to NM_178818.2 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr17:3514080 G>T maps to NM_013276.2 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr17:29220518 A>T maps to NM_024857.3 K1550*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr19:36033312 T>C did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr19:40330914 G>A maps to NM_001436.3 V112V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr2:228399579 C>G maps to NM_001135187.1 G372G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr20:23618487 G>A maps to NM_000099.2 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr22:50649113 C>T maps to NM_031454.1 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr3:47098859 C>T maps to NM_014159.6 Q2138Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr3:141626057 T>C maps to NM_001679.2 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr3:145939878 C>A did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr5:140531289 C>T maps to NM_018939.2 V484V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr5:140751664 G>A maps to NM_018924.2 G568G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr6:26056095 T>C maps to NM_005319.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr8:74464270 A>G maps to NM_001164380.1 Y502Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr1:151678721 T>C maps to NM_007185.4 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr1:197111689 G>T maps to NM_018136.4 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr1:240371138 C>T maps to ENST00000406993 P1152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr10:98741938 T>G maps to NM_015652.2 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr10:112655818 A>G maps to NM_014456.4 K441K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:63065115 A>T maps to NM_001039752.3 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:67763106 A>G maps to NM_030930.2 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr11:118773515 C>A maps to NM_182557.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr12:50746165 G>C maps to NM_001145475.1 L1483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr12:57485519 T>G maps to NM_005967.3 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr13:98667794 A>T maps to NM_002271.4 V797V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr13:113474212 G>A did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr14:74970232 G>A maps to NM_000428.2 C1553C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr15:43653717 T>C maps to NM_152455.3 K704K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr15:85407684 G>A maps to NM_020778.4 L1706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr16:3712966 G>A maps to NM_016292.2 A570A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:7748925 C>A maps to NM_001080424.1 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:12898189 A>G maps to NM_018127.6 C640C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr17:18541948 A>G maps to NM_001039397.2 Y88Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr19:49485592 A>G maps to NM_002103.4 F327F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr2:183594618 G>T maps to NM_018981.1 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr2:198285206 T>C maps to NM_012433.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr2:198365880 A>G maps to NM_002157.2 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr20:18448194 G>A maps to NM_006466.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr22:37898634 C>G maps to NM_014550.3 R587R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr3:69072459 T>C maps to NM_007114.2 Q1050Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr5:153755928 C>T maps to NM_198321.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr6:139694868 A>G maps to NM_006079.3 H71H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr7:4841356 G>A maps to NM_018059.4 G923G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr7:100349674 T>C maps to ENST00000349350 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr7:142640922 C>T maps to NM_000420.2 R513R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr8:7308687 G>T maps to NM_016512.3 S83*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr8:97243647 T>G did not map to a codon.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr9:107578435 C>T maps to NM_005502.3 T1242T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr9:112185014 A>G maps to NM_002829.3 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-A6HP-01A-11D-A31X-10 chr9:131095204 G>A maps to NM_016035.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr1:40733504 A>G maps to NM_005857.3 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr1:53723083 T>G maps to NM_004631.3 V754V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr10:1043229 G>A maps to NM_012341.2 K181K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr10:3172123 A>G maps to NM_002627.3 G599G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr11:61026691 C>A maps to NM_152718.2 E775*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr12:9096394 A>G did not map to a codon.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr14:105412622 A>G maps to NM_138420.2 A3055A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr16:11362954 G>A maps to NM_005425.4 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr16:67183947 C>T maps to NM_033309.2 G147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr16:84940196 G>A maps to NM_031476.3 L481L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr17:47588005 G>T maps to NM_002507.3 V267V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr2:219612346 C>T maps to NM_014640.4 S759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr3:48577176 C>A maps to NM_004567.2 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:27775402 C>T maps to NM_003519.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:31675741 G>A maps to ENST00000375834 W159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr6:32489852 A>G maps to NM_002125.3 L67L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr9:121930243 C>T maps to NM_014618.2 S468S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chrX:70387071 C>T maps to NM_181303.1 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr1:67394624 T>C maps to NM_020948.3 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr12:9754097 T>C maps to NM_002258.2 S61S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr14:93670050 C>T maps to NM_032490.4 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr16:3142578 C>T maps to NM_032805.1 E65E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr16:88694028 G>C did not map to a codon.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr2:138400115 C>T maps to ENST00000272643 C1289C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr2:193056716 T>C did not map to a codon.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr2:219868975 T>C maps to NM_194302.2 P1751P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr5:137506597 C>T maps to NM_139199.1 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chrX:3028195 C>T maps to NM_004042.3 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chrX:114541170 T>A maps to NM_016383.3 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr1:43166451 G>A maps to NM_004559.3 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr1:155408152 T>A maps to ENST00000368346 P1931P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr1:157557284 G>A maps to NM_031282.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr1:214178605 C>T maps to NM_002763.3 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr10:91470808 A>G maps to ENST00000416354 K194K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr10:126715158 A>G maps to NM_022802.2 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr11:597417 G>T maps to ENST00000264555 E248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr11:93090209 G>T did not map to a codon.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr12:6494284 C>T maps to NM_002342.1 I97I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr12:10978001 C>T maps to NM_023921.1 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr12:111758401 G>A maps to NM_015267.3 A863A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr14:58949255 C>T maps to ENST00000354386 L1043L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr16:57494524 C>T maps to NM_020312.3 Q316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr17:37331565 C>T maps to NM_000723.3 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr19:42872695 T>C maps to ENST00000251268 C2121C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr19:50832051 G>A maps to NM_004977.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr19:52222731 G>A maps to NM_001523.2 Y143Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr19:54963392 T>G maps to ENST00000431846 A54A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr19:55603616 G>C maps to NM_017607.2 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr2:46372318 T>C maps to NM_005400.2 N560N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr2:107049612 A>G maps to ENST00000304514 H778H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr2:160982927 T>C maps to NM_000888.3 E615E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr20:3128939 A>G maps to NM_021826.4 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr20:39831714 G>T maps to NM_015035.3 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr22:21330825 G>C maps to NM_144704.2 L343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr22:31837940 T>C maps to NM_019843.3 R790R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr22:50941822 C>T maps to NM_033200.2 K707K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr3:52441416 G>C maps to NM_004656.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr3:73432827 C>T maps to NM_015009.1 A963A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr5:167836949 G>A maps to NM_001161661.1 Q297Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr6:31712028 A>G maps to ENST00000375742 E217E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr7:74212377 T>C maps to NM_173537.2 K491K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr7:100463707 T>C maps to NM_020246.2 D742D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr7:123302929 T>C maps to NM_207163.1 P430P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr9:40774145 C>A maps to NM_033160.5 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr9:137714851 T>C maps to NM_000093.3 P1539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr1:156593854 C>T maps to NM_021817.2 V114V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr11:47788807 A>G maps to NM_015308.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr11:83770382 T>C maps to NM_001142699.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr12:12274104 A>G maps to NM_002336.2 H1599H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr12:29670367 A>G maps to NM_001193451.1 L721L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr14:103430981 C>T maps to NM_006035.3 P861P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr17:10258305 C>G maps to NM_003802.2 L269L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr17:17080726 G>A did not map to a codon.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:1881549 G>A maps to NM_031213.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:41018831 A>G maps to NM_020971.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:45322836 A>C did not map to a codon.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr19:50412017 C>T maps to NM_012346.4 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr2:45800393 C>A maps to NM_018079.4 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr2:73145298 C>G maps to NM_004097.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr2:99689478 A>C did not map to a codon.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr20:470422 C>A did not map to a codon.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr20:44534918 G>A maps to NM_006227.2 D231D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr20:44670174 C>T maps to NM_001134771.1 I377I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr21:45743722 C>T maps to NM_002626.4 I524I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr22:42191443 C>A maps to NM_152513.3 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr3:32860207 C>T maps to NM_001039111.1 C212C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr3:88190086 A>T maps to NM_018293.2 R543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr4:44692822 G>A maps to NM_021927.2 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr5:139193772 T>C maps to NM_032289.2 D280D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr5:140683029 G>A maps to NM_031947.2 Q135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr6:7246993 C>T maps to NM_001003699.3 G1437G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr9:130213581 G>A maps to NM_000976.2 F5F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chrX:68382202 G>A maps to NM_145119.3 T293T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:3679838 A>G maps to NM_152492.2 E374E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:41503103 G>A maps to NM_001031694.2 H526H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:78959186 G>A maps to NM_000959.3 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr1:113657325 C>A maps to NM_014813.1 S786S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr10:32560792 A>G maps to NM_025209.2 H709H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr11:124135726 C>T maps to ENST00000341493 A300A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr11:130785009 T>G maps to NM_014758.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr12:31242980 C>A maps to NM_030653.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr12:102046969 G>T maps to NM_002465.2 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr15:55516127 T>A maps to NM_183235.1 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr16:19073097 A>T did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr17:40726132 G>T maps to NM_016556.2 C107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr17:41365848 C>T maps to NM_145041.1 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr17:45247408 C>T did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr19:36362559 T>A maps to NM_001024807.1 L195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr19:53385206 A>G maps to NM_207333.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr2:20870530 G>A maps to NM_182828.2 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr2:165947166 G>C maps to NM_006922.3 V1832V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr20:33577861 C>T maps to NM_020884.3 L647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr4:128608919 T>C maps to NM_015693.3 H449H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr5:56542172 T>A maps to NM_001127236.2 I182I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr5:66432457 C>G maps to NM_001164664.1 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr5:140188709 C>T maps to NM_018907.2 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr6:147637420 G>A maps to NM_001127715.1 E560E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr7:102769016 C>T maps to ENST00000455523 W142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr8:145003948 C>A maps to NM_201380.2 E1067*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr9:125486285 T>C maps to NM_001005235.1 Y6Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chrX:153588775 G>A maps to NM_001110556.1 T1129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr1:8415615 G>T maps to NM_012102.3 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr1:115601515 G>A maps to NM_005725.4 T144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr10:127731717 C>A did not map to a codon.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr11:74915492 C>T maps to NM_007256.4 F666F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:7023219 A>C maps to NM_006992.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:58149445 C>T maps to NM_138396.4 G45G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:111885275 G>A maps to NM_005475.2 V388V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr12:113596867 G>C maps to NM_001111322.1 R821R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr14:24545746 G>A maps to NM_006032.2 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr2:32664735 T>C maps to NM_016252.3 A1264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr2:202430459 G>T maps to NM_001168221.1 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr2:225449721 G>T maps to NM_003590.3 S2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr22:37770508 C>A maps to NM_052906.3 E356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr22:50684493 A>G maps to NM_032019.5 L560L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr3:3209359 T>C maps to NM_016302.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr4:143159033 A>G maps to NM_003866.2 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr6:2890545 C>A maps to NM_004155.4 E328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr7:78131030 C>A maps to NM_012301.3 V276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr7:99328743 T>A maps to ENST00000292414 K35*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr9:139091692 C>T maps to NM_014564.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chrX:73961091 C>T maps to NM_001008537.2 E1100E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr1:153520964 C>T did not map to a codon.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr11:4869478 A>T maps to NM_001004758.1 G320G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr12:18478008 C>T maps to NM_004570.4 L417L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr15:55731767 T>C maps to NM_130810.2 K265K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr16:4163952 G>A maps to NM_001116.3 C497C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr19:58384711 A>G maps to NM_001144989.1 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr19:58384738 A>G maps to NM_001144989.1 G673G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr2:16085780 C>T maps to NM_005378.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr2:88913361 T>C maps to NM_004836.5 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr2:113079399 C>G maps to NM_198581.2 S348S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr3:183777667 C>T maps to NM_130770.2 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr4:158233958 G>T maps to NM_000826.3 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr6:26217561 G>A maps to NM_021052.2 K120K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr6:36238385 G>A maps to ENST00000457797 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-A5DJ-01A-11D-A26P-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr10:102675795 C>T maps to NM_001136123.1 Q61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr12:53647797 C>T maps to NM_001170790.1 L500L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr15:35189881 T>G maps to NM_014691.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr15:67473651 C>T maps to NM_005902.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr16:2168071 G>A maps to NM_001009944.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:9501595 C>A maps to NM_145054.4 I194I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:38992525 T>G did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:61566073 C>T maps to NM_000789.3 R791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr17:74738355 G>A did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:1506085 G>A maps to NM_213604.2 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:7927063 C>T maps to NM_001159944.1 G567G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:38850107 A>T did not map to a codon.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:46002035 C>T maps to NM_001080401.1 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr19:48205551 C>T maps to NM_015711.3 P1521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr2:203972838 G>A maps to NM_001114132.1 W597*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr2:219222407 C>T maps to NM_198559.1 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr21:45959196 G>A maps to NM_198691.2 R279R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr21:45978022 G>A maps to NM_198696.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr3:97595924 A>T maps to ENST00000182096 K15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr3:122354764 C>T maps to NM_001113523.1 R619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr4:20535254 T>A maps to ENST00000273739 G587G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-AT-A5NU-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:33658353 A>G maps to NM_030955.2 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:135561910 T>A maps to NM_020389.2 R691R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:140176264 C>A maps to NM_018905.2 T572T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr5:167937679 G>T maps to NM_002887.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr6:24357768 A>T maps to NM_016356.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr7:98988629 A>G maps to NM_005720.2 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr7:102553613 G>A maps to NM_145032.3 F309F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr8:67089640 C>T maps to NM_000756.2 A24A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chr8:144808645 T>C maps to NM_198488.3 Q995Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AT-A5NU-01A-11D-A28G-10 chrX:34148841 G>A maps to NM_203408.3 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr1:235386543 T>C maps to NM_016374.5 G334G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr10:104156716 C>T maps to NM_001077494.1 D100D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr11:4904095 A>C maps to NM_001004759.1 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr11:76944147 G>C maps to ENST00000376217 A437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:2909577 T>G maps to NM_002014.3 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:6707539 G>A maps to ENST00000309577 Q512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:42858292 G>A maps to NM_153026.2 Q515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:62795033 T>A maps to ENST00000280377 T914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:105433492 C>T maps to NM_001034173.3 K681K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:120653398 G>A maps to NM_001080855.1 G299G. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B1-5398-01A-02D-1589-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:75516129 T>A maps to NM_001040108.1 K77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:102323021 G>A did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:104027516 A>T maps to NM_001015049.2 T36T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr14:105413290 C>A maps to NM_138420.2 E2833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr15:41854917 T>G did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr15:51993376 A>G maps to NM_013243.3 G381G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr16:31090722 G>A maps to NM_014699.3 E1026E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr16:84063152 A>G maps to NM_001080442.1 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr17:18653136 T>A maps to ENST00000395665 L258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr19:24309779 A>G maps to NM_203282.2 E326E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr19:54872526 C>A maps to NM_002287.3 V120V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:70314949 A>G maps to NM_006196.3 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:166915108 C>T maps to NM_001165963.1 R118R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:180308132 A>G maps to NM_152520.4 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:182765432 T>C maps to NM_001130445.1 L172L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:191797554 A>G maps to ENST00000338435 V588V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:201478583 C>T maps to NM_001159.3 S502S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:227872133 C>T maps to ENST00000396625 Q1660Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:238234212 A>T maps to NM_004369.3 V3161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:239184525 A>C maps to NM_022817.2 S102S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr20:36989401 T>G maps to NM_004139.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr20:57769661 G>A maps to NM_178457.1 A1196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr22:18189423 T>C did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr22:24226510 C>T maps to NM_030807.3 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr22:30069349 T>C maps to NM_181832.2 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr3:25773884 A>T maps to NM_018297.3 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr4:178243704 C>G maps to NM_018248.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:31983431 C>G maps to NM_178140.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:50683583 G>T did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:71739939 G>C maps to NM_152625.1 Y626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:112458402 A>T maps to NM_001085377.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:140222315 G>C maps to NM_018911.2 P470P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr5:173370038 T>G maps to NM_030627.2 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr6:31778273 G>T maps to NM_005527.3 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr6:36040749 C>A maps to NM_139012.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr7:20778603 A>G did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr7:107115464 T>A maps to NM_005295.2 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:214550 G>T maps to NM_152569.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:86485504 T>A maps to NM_017576.1 K896*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:123591453 T>C maps to NM_005047.2 E198E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr9:131339497 T>C maps to NM_001130438.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chrX:2826884 T>C did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:53995547 C>T maps to NM_147193.2 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:151381039 G>A maps to NM_015100.3 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:156268770 C>T maps to NM_001004319.2 W70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:202866047 G>A maps to NM_021633.2 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr1:223286360 G>A maps to NM_003268.5 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr10:103552625 A>G maps to NM_012215.3 Y715Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr13:99481632 G>A maps to ENST00000428223 S1608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr14:50713787 T>C maps to NM_024884.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr14:90870814 C>T maps to NM_006888.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr15:25981204 G>A maps to NM_024490.3 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr15:49293278 A>C maps to NM_001193489.1 V681V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr17:7256620 C>T maps to NM_001002914.2 D120D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr18:72999467 C>A maps to NM_005786.4 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr19:42461227 G>T maps to NM_006423.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr2:12858615 C>A maps to NM_021643.3 I61I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr2:220404815 A>T maps to NM_024536.5 A539A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr20:60908163 G>A maps to NM_005560.3 I1088I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr3:43744052 T>C maps to NM_016006.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr3:113684199 G>A maps to NM_020817.1 I871I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:44450333 A>T maps to NM_198353.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:88053422 C>T maps to NM_001166693.1 C1058C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:100057628 G>T maps to ENST00000505590 I209I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-B1-A47M-01A-11D-A25F-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr4:187093140 A>T maps to ENST00000502894 K34*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr6:26458833 G>A did not map to a codon.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr6:36294404 G>C maps to NM_001010903.4 S306S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr7:66456177 G>C maps to NM_016038.2 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr7:158828653 T>C maps to ENST00000402066 L407L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:16021616 A>G maps to ENST00000445506 D276D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:72182013 G>A maps to NM_000503.4 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr8:124989659 C>T maps to NM_001039112.2 R292*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:6536186 C>A maps to NM_000170.2 V905V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:79325025 G>A maps to NM_015225.2 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:100227198 T>G maps to NM_014290.2 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr10:24873802 T>C maps to NM_020824.3 G1805G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:1281624 T>G did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:46702649 G>A maps to NM_004308.2 F182F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:95825247 C>T maps to NM_032427.1 Q649Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr11:95825253 C>T maps to NM_032427.1 Q647Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr12:132834319 G>A maps to NM_001122636.1 N289N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr13:27332980 C>T maps to NM_005288.3 A328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr15:43571976 C>A maps to NM_052955.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr15:75673956 T>A maps to NM_001145357.1 A1095A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr19:52877550 G>A did not map to a codon.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr20:56140433 C>T maps to NM_002591.3 A481A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr3:48576037 G>T maps to NM_004567.2 G175G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr3:51968674 G>A maps to NM_004704.3 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr4:68534338 T>C maps to NM_018227.5 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr6:31079877 G>T maps to NM_014070.2 G86G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr6:31975053 G>C maps to NM_000500.5 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr6:79918283 G>T maps to NM_004242.2 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chr7:27856558 A>T maps to ENST00000409980 R687*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chrX:53114043 C>A maps to NM_022117.3 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47N-01A-11D-A25F-10 chrX:123185065 C>T maps to NM_001042750.1 F371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr1:22902756 G>A maps to NM_020526.3 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr1:24981474 T>C maps to NM_005839.3 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr1:154680664 C>T maps to NM_002249.4 S661S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr10:55581932 G>A maps to NM_001142763.1 N1858N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr10:111878370 G>T maps to NM_016824.3 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr12:1372210 T>A maps to NM_178040.2 R833R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr12:49259442 A>G maps to NM_014470.3 D36D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr12:53663721 A>T maps to NM_012291.4 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr13:29675027 C>T maps to NM_001033602.2 V865V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr17:7734796 C>G maps to NM_020877.2 S4183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr17:59668145 A>G maps to NM_199290.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr3:123333077 G>A maps to NM_053025.3 C1873C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr6:108533370 A>C maps to NM_003795.4 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr7:82544314 A>G maps to NM_033026.5 S4329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chr9:32571047 G>T maps to NM_002493.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47O-01A-11D-A25F-10 chrX:30237275 C>G maps to NM_002364.4 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr1:186355193 T>C maps to NM_017847.5 D103D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr10:60936660 C>A maps to NM_032439.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr12:100731224 C>T maps to NM_017988.4 L696L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr14:102548765 G>A maps to NM_001017963.2 R713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr16:18864920 G>T maps to ENST00000389467 I1584I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr19:55913034 A>G maps to NM_014501.2 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr2:44547378 A>G maps to NM_000341.3 Q553Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr2:182780850 T>C maps to NM_001130445.1 T828T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr3:46000086 G>C maps to NM_024513.2 Y1204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr3:48699893 G>A maps to NM_001407.2 G58G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr3:189612035 G>C maps to NM_003722.4 A596A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr4:169108557 C>A maps to NM_007193.3 I316I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr6:3137662 C>T maps to NM_004332.2 D200D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr6:168377287 T>C maps to NM_001129895.1 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:15725799 G>A maps to NM_005924.4 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:75615289 T>C maps to NM_000941.2 D573D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr7:151884404 A>T maps to ENST00000355193 T1650T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr8:72958840 G>A maps to NM_007332.2 I656I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A654-01A-11D-A31X-10 chr8:110488891 C>G maps to ENST00000426474 Y2971*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:21936723 G>C maps to NM_001145658.1 V360V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:54707863 G>T maps to NM_145716.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:115221049 A>G maps to NM_000036.2 Y365Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr10:35896875 C>A maps to NM_153368.2 I145I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr10:128830576 T>A maps to ENST00000398025 T614T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr11:1651126 C>T maps to NM_001001480.2 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr11:33374882 T>C maps to NM_005734.3 S1139S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr13:25020899 C>T did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr16:14738463 C>T maps to NM_016561.2 L87L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr16:89713673 C>A maps to NM_001083314.1 E100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:41203098 G>A maps to ENST00000471181 P1793P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:65162706 T>C maps to NM_014877.3 Q594Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:79496378 G>A maps to NM_001077182.2 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr17:79865646 A>G did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr18:9887669 A>G maps to NM_001098529.1 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr18:77659161 G>A maps to NM_012283.1 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr19:49674875 C>T maps to NM_017636.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:1805512 T>C maps to ENST00000399161 E1077E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:27427729 G>C maps to NM_021095.2 L268L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr2:207655322 T>C maps to NM_014929.3 S642S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr21:40665926 G>T maps to NM_018963.3 S214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr21:46924433 A>C maps to ENST00000359759 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr3:51452312 T>G did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr3:154858035 A>G maps to NM_007289.2 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr4:7811365 T>C maps to NM_001134647.1 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:33998824 A>G maps to NM_001167595.1 Y220Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:140745639 C>T maps to NM_018918.2 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr5:176798988 C>T maps to ENST00000398128 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr6:57467162 G>C maps to NM_000947.2 L368L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr6:84233612 C>T maps to NM_153362.2 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr8:145134931 C>T maps to NM_019037.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:35792785 T>C maps to NM_003995.3 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:125315954 C>T maps to NM_001004457.1 T169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr9:134889752 A>G maps to NM_004269.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chrX:71427692 G>T maps to NM_017669.2 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr1:27100917 T>C maps to NM_006015.4 P1400P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr1:111667501 G>T maps to NM_178454.4 C67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr10:51585172 G>A maps to NM_001145260.1 K440K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:27402258 C>G did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:64034707 C>T maps to NM_000932.2 Q1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr11:64813974 G>A maps to ENST00000340252 Y592Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr12:110902938 T>C maps to NM_001164373.1 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr15:71128825 T>C maps to NM_018357.2 G73G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:14678280 T>C did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:30569337 G>T maps to NM_033410.3 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:48576973 G>A maps to NM_153029.3 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr16:50338446 C>T maps to NM_001114.3 N515N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:29533388 G>A maps to NM_001042492.2 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:33288776 C>A maps to NM_052857.3 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:34934556 C>T maps to NM_024835.3 C262C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:40849968 G>T did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:67189984 T>C maps to NM_080282.3 K497K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:72862363 G>A maps to ENST00000442102 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr17:73916510 C>A did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr18:20814664 G>A maps to NM_001100619.2 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:4306031 C>T maps to NM_024333.2 N35N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:4792819 C>A maps to NM_018708.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:10444568 T>A maps to NM_002162.3 T536T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:17056400 G>T maps to ENST00000443236 V974V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:19905759 G>C maps to NM_001099269.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr19:41129531 C>T maps to ENST00000308370 R1260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:11925179 C>T maps to ENST00000396099 S515S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:16082257 A>G maps to NM_005378.4 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:179843224 C>A maps to NM_173648.3 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr2:233898966 C>T maps to NM_005383.2 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr3:13525051 T>G maps to NM_024827.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr3:42218378 G>A maps to NM_001042646.1 E120E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr3:52649429 T>A maps to ENST00000296302 K621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr4:73012853 C>G maps to NM_004885.2 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr4:154542028 C>A maps to NM_001131007.1 S1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr5:176305474 G>A did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr6:30622527 C>A maps to NM_003587.4 L984L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr6:70646795 A>G maps to NM_001858.4 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr6:76640749 G>A maps to NM_001563.2 S721S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr7:28996483 G>A maps to NM_014817.3 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr7:73535229 G>A maps to NM_002314.2 G544G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr7:122081598 A>G maps to NM_001167940.1 G773G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr8:101054050 G>A maps to NM_015668.3 Y639Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr9:85624581 A>T maps to NM_152573.2 Y311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr9:132400145 T>A maps to NM_017873.2 K397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chrX:23723160 G>A maps to NM_001037171.1 I352I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chrX:101152940 A>T maps to NM_001011657.3 I135I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:43394676 G>T maps to NM_006516.2 R334R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:155175048 C>T maps to NM_007112.3 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:197020001 T>C maps to NM_001994.2 K521K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:204379051 A>G maps to NM_032833.3 I496I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr1:240371138 C>T maps to ENST00000406993 P1152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr10:62637690 G>A maps to NM_014836.4 C567C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr11:67267650 G>A maps to NM_004910.2 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr12:12303826 G>C maps to NM_002336.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr13:28367052 C>T maps to NM_145657.1 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr13:98865471 A>G did not map to a codon.
Multiple mappings detected for codon TCGA-B1-A657-01A-11D-A31X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:44105506 C>T maps to NM_005926.2 Q222Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:49304925 A>T maps to NM_001193489.1 S550S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:74325642 G>A maps to NM_033238.2 K515K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr15:85476452 G>A maps to NM_004213.3 P387P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr16:31092684 C>T maps to NM_014699.3 T1680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr17:43009570 C>T maps to ENST00000438933 Q426Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:5214699 G>T maps to NM_002850.3 R1456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:8183904 G>A maps to NM_032447.3 D1071D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:34710314 T>G maps to NM_001114093.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr19:45162148 C>T maps to NM_006505.3 H377H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:12447396 G>C maps to NM_015869.4 R212R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:152163261 C>T maps to NM_021038.3 I247I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:195508982 G>T maps to NM_018406.5 T3156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr3:196888576 A>T maps to NM_004087.2 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr4:76521461 G>T maps to ENST00000307465 S462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr5:176520384 A>G maps to NM_022963.2 R370R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr6:30954812 T>C maps to NM_001010909.2 N287N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr6:31975053 G>C maps to NM_000500.5 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr7:193540 C>T maps to NM_020223.2 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr7:193560 T>A maps to NM_020223.2 L121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chr8:139707080 C>A maps to NM_152888.1 L878L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A657-01A-11D-A31X-10 chrX:79932815 G>T maps to NM_153252.4 P1567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr1:79402058 T>C maps to NM_022159.3 K266K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:105793763 A>G maps to NM_000494.3 A1365A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:129859260 C>A maps to NM_006504.4 I190I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr10:135193908 C>T maps to NM_152911.2 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr12:34179834 A>G maps to NM_032834.3 Q469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr15:40594159 T>A maps to NM_004573.2 K194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr15:72192124 T>G maps to ENST00000424560 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr15:84581895 C>T maps to NM_207517.2 Q585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr16:18844470 G>A maps to ENST00000389467 F2861F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr17:40725219 C>G did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr18:44662720 T>C maps to NM_032124.4 E30E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr18:47500736 C>T maps to NM_001080467.2 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr19:40486338 T>C maps to NM_006503.2 S355S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:48050457 T>G maps to NM_001190274.1 A480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:86371414 T>G maps to NM_006839.2 G751G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:215440517 G>T maps to NM_001080500.2 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr2:233681743 T>A did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:24447424 T>A maps to NM_012295.3 I265I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:32193640 A>T maps to NM_001136029.1 K275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr22:38374015 C>T maps to NM_006941.3 Q185Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:76532404 T>C maps to ENST00000307465 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:90035226 G>T maps to NM_145715.2 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:138450854 G>A maps to NM_019035.3 H796H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr4:146041305 G>A did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr6:150342041 T>A maps to NM_130900.2 G210G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr7:100692246 G>A maps to NM_001040105.1 T4219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr8:121587443 G>A maps to NM_021021.3 Q340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chrX:3238718 A>G maps to NM_015419.3 S1669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chrX:16685794 A>C maps to NM_001144002.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr11:18195247 C>T maps to NM_054032.3 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr12:49445197 A>G maps to NM_003482.3 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr13:29278213 A>G maps to NM_001135919.1 A389A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr17:60766322 T>C did not map to a codon.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr19:2251511 T>A maps to NM_000479.3 G413G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr19:15075129 C>A did not map to a codon.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr5:145719655 G>T maps to NM_002700.2 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr9:33960822 C>G did not map to a codon.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chrX:13635855 T>C maps to NM_001167890.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chrX:114874763 A>G maps to NM_001136025.3 K312K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr1:204183025 G>T maps to NM_198447.1 S3S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr10:122622313 G>A maps to NM_018117.11 G198G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr12:122413566 T>C maps to NM_144668.4 I994I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr14:52182104 G>T maps to ENST00000344768 T304T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr14:68191258 C>T maps to NM_152443.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr18:61058288 T>C maps to NM_004869.3 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr19:10230529 A>G maps to NM_003755.3 P2P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr19:17571477 T>G maps to NM_138454.1 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr22:24581139 C>A maps to NM_019601.3 A287A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr22:43442516 C>G maps to NM_012263.4 L347L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:179094913 T>G maps to NM_033540.2 V394V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:195974372 G>A maps to NM_005017.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:196387839 C>T maps to NM_198565.1 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr4:56301653 A>T maps to NM_004898.2 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr4:69978198 A>G maps to NM_001074.2 L445L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr5:9226980 C>T maps to NM_003966.2 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr7:117364733 T>A maps to NM_033427.2 I1438I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr7:117396641 G>A maps to NM_033427.2 I1105I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr9:14824064 T>G maps to ENST00000380880 V712V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:1334455 G>A maps to NM_030937.4 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:12854435 G>C maps to NM_023013.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:113126669 T>C maps to NM_017744.4 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:148025785 G>A maps to ENST00000310701 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:154493834 G>A maps to NM_001098475.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr1:161183706 C>A maps to NM_004550.4 I450I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr10:21309108 G>A maps to NM_213569.2 F62F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr11:55418711 C>T maps to NM_001004059.2 F111F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr12:49425838 G>A maps to NM_003482.3 Q4217*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:36005047 C>T maps to NM_032594.3 C530C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:45603574 G>A maps to NM_002013.3 L29L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:69256348 C>G maps to NM_004926.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr14:74325602 G>T did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr15:26793189 G>C maps to NM_021912.4 S391*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr15:29368273 C>A maps to NM_005503.3 S350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr15:51857283 C>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:7579414 C>T maps to NM_001126112.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:42828062 C>T maps to NM_145663.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr17:48628384 G>A maps to NM_022827.2 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr19:757668 C>T maps to NM_173481.2 N241N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr19:18279616 G>A maps to NM_005027.2 T630T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:67631298 A>G maps to NM_019002.3 Q495Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:100623249 G>A maps to NM_001025108.1 D264D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:152397246 C>T maps to NM_001164507.1 L6917L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr2:220420910 G>A maps to NM_015311.2 A1480A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr20:62407207 G>A maps to NM_025224.2 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr22:19164389 G>A maps to NM_005984.2 F200F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr22:44564536 C>T maps to NM_001003828.1 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr22:46930991 G>A maps to NM_014246.1 Y692Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:9547648 G>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:19925988 G>C maps to NM_144715.3 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:51667681 C>T maps to NM_015106.2 H305H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:58089734 C>T maps to NM_001164317.1 Y511Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr3:121386443 G>A maps to ENST00000393667 Q3150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr4:1803583 C>A maps to NM_000142.4 I254I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr4:1803748 C>T maps to NM_000142.4 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr5:180048229 C>T maps to NM_182925.4 T681T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr6:32945958 C>G maps to ENST00000395289 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr6:32947798 C>G maps to ENST00000395289 S714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr6:160157287 A>T did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr7:151879015 G>A maps to ENST00000355193 Q1977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr8:53028900 C>T maps to NM_014682.2 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr9:34397496 C>T maps to NM_032596.3 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr9:139008745 T>C maps to NM_152833.2 Q25Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chrX:123176468 C>T maps to NM_001042750.1 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr1:113460276 G>A maps to NM_003051.3 Q251*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr10:50532032 G>A maps to NM_001135196.1 K481K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr10:70547738 T>G maps to NM_018237.2 L979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr12:30888128 C>T maps to NM_001002259.1 A194A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr12:132547146 G>A maps to ENST00000333577 Q2781Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr14:77765101 G>A maps to NM_013382.5 D312D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr15:30008819 A>G maps to NM_003257.3 S1399S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr15:79058943 A>T maps to ENST00000258883 A1103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr17:60484527 T>C maps to NM_001144933.1 H326H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr17:71231746 T>G maps to NM_017941.4 Y42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr19:39226898 G>A maps to NM_144691.3 A478A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr19:54725772 T>C maps to NM_001081450.1 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr2:74742181 C>G maps to NM_016170.4 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr2:113418128 G>A maps to NM_005415.3 L591L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr3:97673273 G>T maps to NM_153182.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr3:149678839 C>T maps to NM_007282.4 V365V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr4:56765983 A>G maps to NM_018261.3 Q757Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr5:82850837 G>A maps to NM_004385.4 W3239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr6:82461774 G>T maps to ENST00000369756 G109G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr6:108227976 A>G maps to NM_007214.4 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chrX:53589173 C>T maps to ENST00000276009 E2412E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:11273602 G>C maps to NM_004958.3 T1046T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:22927185 A>T maps to NM_020526.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:89528890 G>T maps to NM_002053.2 G9G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:207105905 C>A maps to NM_002644.3 G635*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr1:240371660 A>C maps to ENST00000406993 G1326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr11:32954929 C>A maps to NM_001076786.1 S580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr12:41585334 C>T maps to NM_001164595.1 R242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr12:130184818 C>G maps to NM_133448.2 L168L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr13:52548107 A>T maps to NM_000053.2 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr14:24613238 C>T did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:41146020 C>T maps to NM_181642.2 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:43724400 G>A maps to NM_001141980.1 L1222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr15:94841733 C>T maps to NM_018349.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr17:66270211 C>A did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr19:2216710 G>A maps to ENST00000221482 L785L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr19:15164632 C>T maps to NM_012114.2 H89H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr19:22817126 T>G did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr19:40395977 G>A maps to NM_003890.2 G2473G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr2:27565919 G>T maps to NM_001521.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr2:42488419 T>C maps to NM_019063.3 A166A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr2:109527286 C>T maps to ENST00000376651 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr21:47626683 T>G did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr3:142274791 A>T maps to NM_001184.3 S756S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:89039326 A>G maps to NM_004827.2 L259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:115767017 G>A maps to NM_022569.1 I692I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr4:177136795 T>C maps to NM_080874.3 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr5:43490824 C>A maps to NM_198566.2 V529V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr5:150660716 G>T maps to NM_001145017.1 Y375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr5:179248067 C>T maps to NM_003900.4 C44C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr7:35912376 G>A did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr7:149129442 C>T maps to ENST00000440594 E641E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:94054730 C>T maps to NM_003567.2 Q244Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:151678721 T>C maps to NM_007185.4 Q368Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr1:153279660 G>C maps to NM_052891.1 Y46*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:1466622 C>T maps to NM_003957.2 D304D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:111590500 C>T maps to NM_015191.1 V423V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr12:64615825 G>C maps to ENST00000311915 A64A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr13:25067775 T>C maps to NM_006437.3 E279E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr14:35593086 T>C maps to NM_014672.2 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr14:102675937 T>C maps to ENST00000454394 D508D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr17:37876079 A>C maps to NM_004448.2 R647R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr17:42275085 C>A maps to NM_020218.1 E22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr18:23969873 T>C maps to ENST00000418698 R834R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr19:11558372 A>G maps to ENST00000436195 E323E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr2:189912940 T>C maps to NM_000393.3 G1065G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr2:202262966 G>A maps to NM_015049.2 F197F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr2:218954704 C>T maps to NM_198483.3 C548C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr20:3090942 G>A maps to NM_014948.2 L479L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr4:5721078 G>A maps to NM_153717.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr4:69816983 A>G maps to NM_024743.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:9119219 A>T maps to NM_003966.2 S605S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:34757667 C>T maps to NM_001145521.1 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr5:93076681 A>T maps to NM_153216.1 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr6:12123739 T>C maps to NM_002114.2 L1238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr7:19738025 T>C maps to NM_001002926.1 K310K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr7:82763634 A>G maps to NM_033026.5 N1077N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr8:99441266 G>T maps to NM_020697.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr8:139163999 G>T maps to NM_015912.3 G906G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr9:133748370 C>T maps to NM_007313.2 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:27121058 C>T maps to NM_017837.2 F178F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:27428599 C>T maps to NM_003047.3 L614L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:85491699 A>G maps to NM_018298.9 N339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr1:160105303 C>A maps to NM_000702.3 G732G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr10:89624274 C>T maps to NM_000314.4 Q17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr10:126477650 A>G maps to NM_212554.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr11:6486811 C>T maps to NM_033278.2 L38L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr11:62519738 G>A maps to NM_024784.3 Y516Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr11:133814178 C>A maps to NM_014987.1 V115V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr12:53587038 G>A maps to NM_000889.1 C537C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:60749543 G>T maps to NM_177952.2 T114T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:68282658 C>A maps to NM_015346.3 E8*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:95556879 G>T maps to NM_177438.2 A1908A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr14:105222012 C>T maps to NM_006427.3 D55D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr15:43733776 A>G maps to NM_001141980.1 P1015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr15:89399907 T>C maps to NM_013227.3 T1364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr16:1251874 C>T maps to NM_021098.2 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr16:57562849 C>A maps to NM_033212.3 L80L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr17:7464140 G>A maps to NM_003808.3 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr19:41223384 A>T maps to NM_025194.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr19:49167944 A>C maps to NM_145807.1 G237G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr20:19956189 C>T maps to ENST00000255006 F556F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr20:37356312 C>T maps to NM_080552.2 G203G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr3:17053309 G>C maps to NM_001144382.1 L820L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr3:36873054 C>T maps to NM_014831.2 L2629L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr4:3201561 C>T maps to NM_002111.6 S1824S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr4:84243393 G>A maps to NM_006665.5 Y117Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr4:159092401 A>T maps to NM_001128424.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr5:134002686 G>A did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr7:5415787 G>A maps to NM_001080495.2 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr7:75028468 A>G maps to ENST00000430211 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr7:100224940 C>A maps to NM_003227.3 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr8:36698473 C>A maps to NM_001031836.2 L552L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr9:35243361 G>C did not map to a codon.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr9:117052532 C>G maps to NM_032888.2 G1430G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr1:231502191 T>A maps to NM_022051.2 K416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr1:249150135 A>G maps to NM_001136036.2 P228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr10:99192202 C>T maps to NM_002629.2 P229P. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr11:12225945 G>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr11:65305493 G>A maps to NM_020680.3 W696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr11:133805657 C>T did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr12:81661719 A>G maps to NM_003625.2 L1153L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr13:21295993 C>T maps to NM_138284.1 V170V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:19884047 G>A maps to NM_016235.1 D40D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:30899186 C>T maps to NM_004765.2 *218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:56531662 G>A maps to NM_031885.3 L597L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr16:88653022 G>T maps to ENST00000452588 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:4800539 T>G maps to NM_153827.4 V1319V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:7324266 C>A maps to NM_199339.2 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:15964733 A>G maps to ENST00000395857 S1969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:40821476 C>A maps to NM_024927.4 E726*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr19:1555891 G>A maps to NM_001174118.1 S542S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr19:3110144 A>C did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr19:10132217 C>A maps to NM_015725.2 V243V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr2:27305347 C>T maps to NM_007046.3 S303S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr2:70037723 A>G did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:5903026 A>G maps to NM_001819.2 T79T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:21376575 G>T maps to NM_033176.1 A346A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:61833791 T>C maps to NM_017798.3 K500K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr21:46925136 T>C maps to ENST00000359759 P1401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr21:46925139 C>A maps to ENST00000359759 P1402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr22:18028579 T>A maps to ENST00000400579 P1180P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr22:24041047 A>T maps to ENST00000382833 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:49946455 G>A maps to NM_032355.3 L650L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:52027875 G>T maps to NM_000992.2 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:69096706 T>C maps to NM_007114.2 T383T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:110830988 G>A maps to NM_015480.1 W91*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr3:196675119 A>T maps to NM_025163.2 L216L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr4:39325031 C>T maps to ENST00000381897 E216E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr4:80992808 C>A did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr6:158449968 A>T maps to NM_003898.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:97933660 G>A maps to NM_018842.4 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:151262971 C>T did not map to a codon.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr8:144660317 G>T maps to ENST00000276844 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chrX:15841259 C>G maps to NM_005089.3 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr1:20304928 G>A maps to NM_001161728.1 F43F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr1:211545689 C>A maps to ENST00000427925 Y451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr10:70196868 A>C maps to NM_001080449.1 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr10:115608964 A>G maps to NM_014881.3 R633R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr11:61161356 T>G maps to NM_001173991.2 G46G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr11:92533291 C>T maps to ENST00000298047 F2371F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:988848 A>C maps to NM_018979.3 G828G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:7654023 A>C maps to NM_004244.4 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:64803741 A>G did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:104030937 G>C maps to NM_017564.9 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr12:130892348 A>C maps to NM_015347.4 R949R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr13:32906982 G>A maps to NM_000059.3 E456E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr14:31355024 C>T maps to NM_004086.2 F328F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr14:62463093 A>C maps to NM_031914.2 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr16:48286155 G>A maps to NM_031490.2 E116E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr16:72984697 G>A maps to NM_006885.3 G962G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:8047042 T>G maps to NM_002616.2 P871P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:33586029 T>G maps to NM_144975.3 G107G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:40344971 C>T maps to NM_032484.4 Q113Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr17:71196857 G>A maps to NM_018714.2 E408E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr18:20716292 C>A maps to NM_001100619.2 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:5131902 G>C maps to NM_015015.2 P597P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:13875776 C>T maps to NM_001031727.2 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:36353425 A>G maps to NM_199180.2 G514G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:39039029 T>C maps to NM_000540.2 R4084R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:40366037 C>G maps to NM_003890.2 P4732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:51170083 C>A maps to ENST00000391814 G1719G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:53668283 T>A maps to NM_024733.3 K487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr19:54783676 C>T maps to ENST00000391747 E125E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:20818845 C>T maps to NM_022460.3 Q360Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:27840356 A>G maps to NM_032434.2 G438G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:32289268 C>G maps to NM_014946.3 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:33813449 A>G maps to ENST00000395190 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:105858581 C>G maps to NM_007227.3 P89P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:121746537 C>T maps to NM_005270.4 D1016D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr2:202626256 G>A maps to NM_020919.3 Q154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr21:35468405 C>G maps to NM_006933.4 G303G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr22:30000102 T>G did not map to a codon.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr22:41543892 G>A maps to NM_001429.3 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:127774578 C>T maps to ENST00000464451 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:142607734 T>G maps to NM_013363.3 R2R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:154055934 A>G maps to NM_001038705.1 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr3:184019769 C>T maps to NM_002808.3 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr4:62542579 T>G maps to ENST00000506720 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr4:141580760 G>C maps to NM_015130.2 Y634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr5:156482503 A>C maps to NM_001173393.1 G29G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:11005703 A>C maps to NM_017770.3 G52G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:17507927 T>C maps to NM_006366.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:109764876 A>G maps to NM_003080.2 G347G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:119282963 T>G maps to NM_024581.4 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr6:144086446 G>C maps to NM_001100164.1 S248S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:75028468 A>G maps to ENST00000430211 P84P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:100675713 G>C maps to NM_001040105.1 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:135290918 A>G maps to NM_015135.2 G950G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:142724165 C>G maps to NM_001001658.1 G18G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:150033985 C>G maps to NM_023942.2 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr7:150500796 C>A maps to NM_018487.2 Y144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr8:103300467 T>C maps to NM_015902.4 G1580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr9:8507426 C>G maps to NM_002839.3 G517G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr9:35089136 A>C maps to NM_032634.2 G1074G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chr9:35711015 C>T maps to NM_006289.3 K1361K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chrX:54578751 A>C maps to NM_019067.5 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chrX:70387443 G>C maps to NM_181303.1 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4117-01A-01D-1252-08 chrX:134990741 A>G maps to NM_018666.2 G469G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr1:21585299 G>T maps to NM_001397.2 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr1:27682528 G>A maps to NM_004672.3 G1233G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr1:110768795 G>A maps to NM_004978.4 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr11:46897383 G>A maps to ENST00000256991 Q1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr11:66411449 T>A maps to NM_001198845.1 A289A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr11:69625369 A>C maps to NM_005247.2 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr12:52756664 C>G maps to NM_002283.3 T350T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr12:124093347 A>T maps to NM_020936.1 R175*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr14:53019984 G>C maps to NM_001099652.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr16:67681656 T>C maps to NM_001013838.1 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr17:7230248 G>A maps to NM_032442.2 N291N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr17:53398134 G>A maps to NM_002126.4 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr2:179307991 A>T did not map to a codon.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr20:20269293 G>A maps to ENST00000389655 T949T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr21:46929448 C>T maps to ENST00000359759 Y1558Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr3:44776080 A>G maps to NM_145044.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr3:63973880 G>A maps to NM_001177387.1 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr3:73673577 G>C maps to NM_015009.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr9:7169907 C>T maps to NM_001146694.1 C1004C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr1:18023595 G>A maps to NM_018125.3 L1187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr1:85656154 T>C maps to NM_032184.1 V342V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr1:90179253 T>C maps to NM_032270.4 H375H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr1:180904787 G>A maps to NM_020950.1 R581R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr1:230907779 A>G maps to NM_006615.2 R270R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr11:1017454 C>T maps to NM_005961.2 V1782V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr11:1093115 C>T maps to ENST00000441003 T1645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr11:117869596 A>T maps to NM_001558.3 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr12:51138541 G>T maps to NM_173602.2 G1551*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr12:111895016 C>G did not map to a codon.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr13:47269133 G>A maps to NM_001164211.1 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr14:105621903 C>T maps to NM_002226.3 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr15:63548781 A>T maps to NM_016530.2 R135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr15:83935686 C>A maps to NM_001717.3 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr16:72992085 G>C maps to NM_006885.3 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr17:18220176 T>C maps to NM_144775.2 D358D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr17:79411727 C>T maps to ENST00000436173 P849P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr19:1220438 A>T maps to NM_000455.4 K178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr2:15735616 C>T maps to NM_004939.1 L24L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr2:88478332 G>A maps to NM_018271.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr20:30064535 G>A maps to NM_014012.4 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr20:54974309 T>A maps to NM_001033522.1 S311S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr21:39671713 C>T maps to NM_170736.1 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr5:112200370 A>G maps to NM_003135.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr5:140563849 C>T maps to NM_020957.1 C572C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr5:140573840 C>T maps to NM_018930.3 C572C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr6:17292211 G>A maps to NM_001143942.1 G191G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr6:32147441 G>A maps to NM_006913.3 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr6:51923119 C>A did not map to a codon.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr6:74119026 G>A maps to NM_018665.2 K412K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr6:111213403 T>C maps to NM_001634.4 C156C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr7:90042217 A>G maps to NM_001185072.2 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr7:103002481 G>T maps to NM_002803.2 V123V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr7:141408684 A>T maps to NM_001105558.1 K43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr9:98229470 C>A maps to NM_000264.3 V829V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr9:123742456 A>G maps to NM_001735.2 L1188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr9:139399212 G>A maps to NM_017617.3 L1644L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:19166251 C>G maps to NM_152232.2 L787L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:150390093 T>C maps to NM_015203.3 N76N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr12:26553126 G>A maps to NM_002223.2 T2488T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr13:39452996 C>G maps to NM_207361.4 T2963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr14:24805464 G>T maps to NM_006871.3 P491P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr15:72104833 C>T maps to NM_014249.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr16:1815159 G>A maps to NM_015133.3 L808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr16:46766186 C>T maps to NM_182493.2 R465R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr17:8370301 T>C maps to ENST00000402554 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr19:3527658 C>A maps to NM_001136198.1 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr19:50063189 C>G did not map to a codon.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:58431303 A>G maps to NM_001114636.1 S144S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:74275020 C>T maps to ENST00000409262 P566P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:145156026 G>A maps to NM_014795.3 F909F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr2:207564615 T>C did not map to a codon.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr3:97852335 G>A maps to NM_001005338.1 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr3:197553819 C>A maps to ENST00000425562 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr4:72620173 G>A maps to ENST00000504199 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:31323225 T>G maps to NM_004932.2 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:114515695 G>A maps to NM_018700.3 I13I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr5:140712437 A>G maps to NM_018912.2 G729G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr7:150325337 G>A maps to ENST00000438845 I186I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chrX:50350697 C>T maps to NM_020717.3 E1148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:40029529 C>T maps to NM_001135653.1 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:151259372 C>G maps to NM_020832.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:152957849 C>T maps to NM_005987.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr1:153004964 C>T maps to NM_003125.2 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:85449851 G>T maps to NM_001079910.1 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:102125408 T>C maps to ENST00000449403 Q204Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:131590406 C>A maps to NM_198827.3 G628G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr14:24728419 C>A maps to NM_000359.2 G340G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr14:61434958 T>C maps to NM_002431.3 H274H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr16:2153594 G>A maps to NM_001009944.2 D2821D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr17:14005507 T>A maps to NM_001303.3 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr17:77984463 C>A maps to NM_019020.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr19:11144468 C>A maps to NM_001128849.1 G1267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr19:50017711 G>T maps to NM_004107.4 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr19:52660095 G>A maps to NM_001102657.1 G280G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr2:27668214 G>T maps to NM_015662.1 A1672A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr2:27704120 A>G maps to NM_015662.1 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr2:125627296 G>T maps to NM_130773.2 E1131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr2:170101422 C>A maps to NM_004525.2 S1070S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr2:218712983 G>C maps to NM_022648.4 P627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr3:113376679 G>T maps to NM_001009899.2 G1283G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr4:169931207 G>T maps to NM_032783.4 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr4:177046438 C>A maps to NM_170710.4 P265P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr5:13922242 C>A maps to NM_001369.2 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr8:8235102 A>T maps to NM_001080826.1 T272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr8:99215363 A>T maps to NM_024759.1 I284I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr9:117400850 T>C maps to ENST00000374049 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chrX:35985763 G>T maps to NM_152632.3 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chrX:53607788 A>G did not map to a codon.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chrX:133379027 T>C maps to NM_001101357.1 Y66Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr1:1179847 G>C maps to NM_001014980.1 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr1:200376814 T>C maps to NM_012482.3 Q673Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr10:87484286 T>G maps to NM_017551.2 P560P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr11:1093325 C>A maps to ENST00000441003 G1715G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr12:49690228 C>T maps to ENST00000451891 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:43771710 T>C maps to NM_001141980.1 E224E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:43940127 G>A maps to NM_172095.1 I44I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr15:102346641 G>T maps to NM_001005326.1 L240L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr17:55197615 G>A maps to ENST00000427138 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr17:61623067 A>G maps to NM_030779.2 A930A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:1059068 G>T maps to NM_019112.3 G1816G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:12502557 C>T maps to NM_001080821.2 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:18288014 C>T maps to NM_006332.3 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:32873420 T>A maps to NM_014910.4 S803S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr19:49114032 G>A maps to NM_017708.3 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:107073431 G>A maps to ENST00000304514 L134L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:114391750 G>A maps to ENST00000409875 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:166153544 A>T maps to NM_001040142.1 K96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:170055305 A>G maps to NM_004525.2 P2856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:238275564 C>T maps to NM_004369.3 S1755S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr2:242407763 C>G maps to NM_014808.2 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr20:40143494 C>A maps to NM_032221.3 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr20:42328635 C>T maps to NM_002466.2 I301I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr3:57743530 A>G maps to ENST00000428312 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr3:195507743 A>C maps to NM_018406.5 L3569L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr5:37834924 C>A did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr5:140595248 T>C maps to NM_018933.2 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr5:148730493 C>T maps to NM_152407.3 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr6:35086063 T>G maps to NM_001093728.1 T511T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr6:90402312 G>C maps to NM_014611.1 S3479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr6:142691577 C>T maps to NM_198569.2 V239V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:2959067 G>A maps to NM_032415.4 C816C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:49815192 C>T maps to NM_198570.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:91957149 T>C maps to NM_019004.1 I241I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:106799966 T>A maps to NM_002736.2 Y399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr8:108970371 T>C maps to NM_178565.4 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr9:36583633 A>G maps to NM_014791.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chrX:23723675 G>A maps to NM_001037171.1 F323F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chrX:67283720 G>A maps to NM_002547.2 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr12:56558429 A>C maps to NM_003075.3 G1075G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr19:53057179 T>C maps to NM_001039886.3 H337H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr2:54855277 G>C maps to NM_003128.2 V563V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr2:179255927 G>A maps to ENST00000392505 K835K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr22:43569807 G>T maps to NM_015140.3 C418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr5:172659919 C>G maps to NM_004387.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr7:123302917 T>C maps to NM_207163.1 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W7-01A-11D-A31X-10 chr7:128804349 C>A maps to NM_178562.3 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr1:2938840 C>A maps to NM_080431.4 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr1:151146998 T>A maps to NM_013353.2 R50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr10:115917413 G>A maps to NM_018017.2 Q220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr11:82879803 A>T maps to NM_015885.3 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr11:95825355 T>C maps to NM_032427.1 Q613Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr11:95825394 C>T maps to NM_032427.1 Q600Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr12:64808727 C>A maps to NM_007235.3 A34A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr13:25672006 A>G maps to NM_030979.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr13:32841387 C>A maps to NM_023037.2 A2676A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr15:42147763 G>A maps to ENST00000320955 S3067S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr15:65369366 C>T maps to NM_001101362.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:30794424 G>A maps to NM_001080417.1 G408G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:58074477 C>A maps to NM_002428.2 G262G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:69727577 C>T maps to NM_138713.2 Q1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:83994294 G>A maps to NM_013370.3 W192*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr16:86565820 G>A maps to NM_001159377.1 D316D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:8424547 G>A maps to ENST00000360416 G671G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:27902917 T>C did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:40028341 A>T maps to ENST00000401700 I956I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr17:48541576 A>G did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr19:11134285 C>G maps to NM_001128849.1 V984V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr19:39687742 C>T maps to NM_001001414.1 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr3:48336156 T>C maps to NM_005793.3 V185V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr3:50147867 T>C maps to NM_005778.2 P445P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:5754738 G>A maps to NM_153717.2 Q425Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:6860176 G>A maps to NM_014743.2 E154E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:40818109 T>A maps to NM_004307.1 *760L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr4:48536645 A>G maps to NM_015030.1 S2207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:131602210 C>T maps to NM_003687.3 H100H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:131647951 A>C maps to NM_003059.2 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:134785314 G>C maps to NM_001099221.1 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr5:161116040 T>C maps to NM_000811.2 N104N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr6:24701749 A>T maps to NM_018473.3 G110G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr7:1477989 C>G did not map to a codon.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr7:107398635 C>T maps to NM_024814.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr7:108212286 G>A maps to NM_012328.2 E39E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr8:24771575 C>T maps to NM_005382.2 P90P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr8:145001216 C>T maps to NM_201380.2 A1428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chr9:21971183 T>G maps to NM_001195132.1 R58R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W8-01A-11D-A28G-10 chrX:70618523 G>A maps to ENST00000449580 K1240K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr1:95330397 T>A maps to NM_001114106.1 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr1:146696656 T>A did not map to a codon.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr1:225546328 T>C maps to NM_001373.1 T3824T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr10:71128299 G>A maps to ENST00000439900 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr10:119003519 G>T maps to NM_003054.4 E54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr15:43571976 C>A maps to NM_052955.2 L508L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr16:4432542 A>C maps to NM_138440.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr16:72821092 G>T maps to NM_006885.3 T3694T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr16:88889079 G>A maps to NM_000512.4 V427V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr18:50985742 T>A maps to NM_005215.3 S1178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr19:14044011 G>A maps to NM_024825.3 L349L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr19:19822256 T>G maps to NM_021030.2 G611G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr2:39088915 T>C maps to NM_198963.1 A212A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr2:178936707 G>A maps to NM_016953.3 R153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr2:234102515 G>T maps to ENST00000359570 T835T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr3:133331388 C>T maps to NM_007027.3 L1293L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr4:128813595 T>C maps to NM_014264.4 Y705Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr5:137289149 G>A maps to NM_016603.2 R553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr6:47254096 G>A maps to NM_014452.3 Q111*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A5W9-01A-11D-A28G-10 chr8:37978551 G>A maps to NM_004674.3 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:21889673 C>A maps to NM_000478.4 A123A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:87570376 T>C maps to NM_012262.3 *357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:155292769 A>C maps to NM_001105203.1 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr1:248059781 G>A maps to NM_001001957.2 K298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr11:17099462 A>G did not map to a codon.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr11:104901191 A>C maps to NM_033292.2 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr14:31081504 G>A maps to NM_017769.3 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr15:90321561 C>T maps to NM_001039958.1 Y397Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:27549610 C>T maps to NM_001520.3 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:68853182 A>C maps to NM_004360.3 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr16:89650106 T>A maps to NM_014427.4 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr17:76921134 G>A maps to NM_003255.4 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr18:46798649 C>G maps to NM_017653.3 L383L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:1082888 G>T maps to NM_012292.2 L856L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:17366409 G>A maps to NM_031941.3 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr19:52376954 A>G maps to NM_032679.2 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr2:127950813 G>T maps to NM_001001665.3 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr2:175614799 G>A maps to NM_001039523.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr5:908119 C>T maps to NM_004237.3 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr5:55212821 T>C maps to NM_139017.4 G723G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr5:149921205 C>T maps to NM_001543.4 L608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr6:121433800 G>T maps to ENST00000275159 C1099*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr7:100466247 C>T maps to NM_003302.2 G165G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chr9:129870362 T>G maps to NM_012098.2 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-A69E-01A-11D-A31X-10 chrX:118977250 T>C maps to NM_080632.2 R161R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr1:32203281 G>A maps to NM_001703.2 T949T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr1:65895650 C>A maps to NM_017526.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr1:159169658 G>A maps to NM_021189.3 R391R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr11:840427 G>A maps to NM_021128.4 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr11:6411959 G>T maps to NM_000543.4 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr11:77934563 G>A maps to NM_080491.2 D487D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr12:48538848 C>A maps to NM_001166686.1 A747A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr12:118462709 C>A maps to NM_007370.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr14:73412734 G>A maps to NM_015604.3 K226K. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BQ-5875-01A-11D-1589-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:7250506 G>A maps to NM_014716.3 W430*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:47299546 T>C maps to NM_016428.2 P299P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:74772620 C>T maps to NM_024311.2 Q395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr17:78858926 C>T maps to NM_020761.2 D654D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr19:17396341 C>T maps to NM_152363.4 A493A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr19:44635910 A>C maps to NM_013362.2 R382R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr2:47300863 C>T maps to ENST00000394850 G817G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr2:204305854 C>T maps to ENST00000374493 P738P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr22:30038222 C>A maps to NM_181832.2 Y132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr3:4685827 A>T maps to ENST00000356617 I174I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr3:47061275 T>A maps to NM_014159.6 K2469*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr5:132270291 T>G maps to NM_014423.3 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr7:40134551 A>G maps to NM_003718.4 R1504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr7:114299728 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr8:28209092 C>A maps to NM_018660.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr8:144998456 C>T maps to NM_201380.2 L2017L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr9:79955423 T>A maps to ENST00000376646 A2328A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chrX:46491074 A>T maps to NM_032591.1 V561V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:2415963 C>T maps to NM_014638.2 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:12327037 T>C maps to NM_015378.2 T565T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:78325732 T>C maps to NM_198549.2 L399L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:100572513 A>C maps to NM_194292.1 V454V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr1:185984289 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr11:65113197 G>A maps to NM_006268.3 L233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr11:77412779 T>C maps to NM_016578.3 K498K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr11:130785819 T>A maps to NM_014758.2 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr12:19665399 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr12:123479958 C>T maps to NM_020845.2 Q677Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr15:41854917 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr15:68479998 T>C maps to NM_016166.1 S594S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr17:6942203 C>G maps to NM_201566.2 L359L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr18:44639348 A>T maps to NM_032124.4 T225T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:55566740 T>G maps to ENST00000436346 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:100015353 A>C maps to NM_015904.3 T1179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:136873380 G>T maps to NM_001008540.1 I43I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:196749320 T>C maps to NM_018897.2 Q1917Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr22:16287579 G>T maps to NM_001136213.1 C102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr22:42342455 C>G maps to NM_024053.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr4:69202907 C>T maps to NM_001031732.2 E240E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr5:16764478 G>T maps to NM_012334.2 A402A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr5:89989973 A>T maps to NM_032119.3 T2467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr5:140865324 C>G maps to NM_018928.2 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr6:43275359 T>C maps to ENST00000449267 Q106Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr8:38314949 C>T maps to NM_001174067.1 K38K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chrX:70643917 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chrX:134303601 A>G maps to NM_001031705.2 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr1:186072769 A>G maps to NM_031935.2 G3580G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr10:55626410 G>A maps to NM_001142763.1 A1241A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr10:75037056 G>A maps to NM_145170.3 Q891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr14:75265653 C>A maps to NM_019589.2 L1218L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr15:45445602 G>C maps to NM_175940.1 V1150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr15:65490141 G>A maps to NM_003613.3 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr16:2817458 T>C maps to NM_016333.3 S2310S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr16:55705979 C>T maps to NM_001043.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr17:10366487 G>A maps to NM_017533.2 R275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr17:39183128 A>G maps to NM_031957.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr17:44806263 G>A maps to NM_006178.2 Q624Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:1986876 C>G maps to NM_017797.3 P456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:11326076 T>C maps to ENST00000319867 S1364S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:41018831 A>G maps to NM_020971.2 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr19:50200611 C>A maps to NM_152359.2 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr2:109392303 T>C maps to NM_006267.4 I2803I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr22:30050708 A>T maps to NM_181832.2 K171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr3:20187857 C>T maps to NM_003884.4 Y685Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr3:183013204 G>A maps to NM_015078.2 Q520*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr5:172410943 C>T maps to NM_003945.3 F27F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr6:7562979 T>A maps to NM_004415.2 Y231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chr7:48284202 G>A maps to NM_152701.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5877-01A-11D-1589-08 chrY:14847583 A>G maps to NM_004654.3 L232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr1:6204187 G>A maps to NM_015557.2 Y610Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr1:11562883 G>T maps to NM_020780.1 E416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:23003186 G>A maps to NM_005028.4 F23F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:44112495 C>T maps to NM_145312.3 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:55583105 G>C maps to NM_001142763.1 L1467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:75457453 T>C maps to NM_001144000.1 Q20Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr10:102683798 C>T maps to NM_001136123.1 S347S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr11:1466526 G>C maps to NM_003957.2 G272G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr11:5068081 C>T maps to NM_001001916.2 F109F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr11:62458108 C>T maps to NM_001130702.1 E403E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr12:10766046 G>T maps to NM_018048.3 R29R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr12:121465529 C>A maps to NM_003733.2 E250*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr14:23467860 A>C maps to NM_021944.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr14:55818481 C>T maps to NM_152231.1 I458I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr15:87217501 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr16:48385616 T>C maps to NM_031490.2 F821F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr16:72110799 G>A maps to ENST00000228226 Q326Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr17:80525989 C>T maps to NM_004514.3 G225G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr18:55996284 C>A maps to NM_001144967.1 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr19:12875720 C>T maps to NM_013312.2 R578R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:20871055 C>T maps to NM_182828.2 D408D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:74756586 G>C maps to ENST00000258081 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:179452052 C>T maps to NM_133378.4 G18727G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:207833967 G>C maps to NM_173077.2 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:215840567 A>G maps to NM_173076.2 Y1774Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr20:33762616 A>T maps to NM_006404.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr22:32301996 T>G maps to NM_001136029.1 S1479S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:33135654 C>T maps to NM_001039770.2 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:41274904 C>T maps to NM_001904.3 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:51697405 C>T maps to NM_015106.2 D1458D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr3:69101210 G>A maps to NM_007114.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr4:151827109 A>T maps to NM_006726.3 L545L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:446364 G>A maps to ENST00000315013 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:136328173 G>A maps to NM_004598.3 G235G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:137715372 T>C maps to NM_016604.3 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr5:139197068 C>T maps to NM_032289.2 N340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:34210571 G>A maps to NM_145899.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:112457350 G>A maps to NM_001105206.1 Q1130*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:148808751 C>G maps to NM_015278.3 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr6:151751271 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr7:92078079 T>A maps to NM_021167.3 I88I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr9:137300035 C>T maps to NM_002957.4 I107I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chrX:154130374 G>T maps to NM_000132.3 G2022G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr1:156105084 C>T maps to NM_170707.2 L306L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr1:223401080 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr10:33211663 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr13:25672006 A>G maps to NM_030979.2 L557L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr17:10554907 G>A maps to NM_002470.2 G142G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr17:61995167 G>T maps to NM_000515.3 V136V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr2:152372971 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr20:2998528 C>T maps to NM_002836.3 V337V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr20:31024235 G>T maps to ENST00000375687 E1241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr3:197501075 T>C maps to NM_032288.6 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr4:119273491 A>T maps to NM_003619.3 A128A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr5:1094289 C>T maps to NM_006598.2 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr8:144898884 G>A maps to NM_078480.1 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr9:215108 G>T maps to NM_152569.2 L96L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chrX:132160220 A>C maps to NM_031907.1 P676P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr1:984365 C>T maps to NM_198576.2 L1409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr1:41976754 G>C maps to NM_024503.3 P2196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr1:45476718 G>A maps to NM_024602.5 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:1093409 C>A maps to ENST00000441003 T1743T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr11:55904465 C>T maps to NM_001004064.1 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr14:68157016 G>A maps to NM_016026.3 G192G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr18:7025997 A>G maps to NM_005559.2 P794P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr18:74622685 C>T maps to NM_007345.3 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr2:111399712 G>A maps to NM_004336.3 Q816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr20:47271872 G>A maps to NM_020820.3 Q722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr22:26400726 C>T maps to ENST00000407587 Q2128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr4:3124640 T>C maps to NM_002111.6 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr4:72429511 T>A maps to NM_001098484.2 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr4:107163638 G>A maps to NM_001163436.1 C386C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr6:35949920 C>T maps to NM_052961.3 T334T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr7:21468914 G>A maps to NM_003112.3 Q44Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr7:134133230 T>C maps to NM_001628.2 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chr9:35751269 G>A maps to ENST00000456972 Q205Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chrX:43702914 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr1:6399499 G>T maps to NM_007274.3 I137I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr1:9064924 C>A maps to NM_207420.2 S402S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:1093391 C>T maps to ENST00000441003 T1737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr11:62417116 A>G maps to NM_030628.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr12:31944971 A>G maps to NM_001013699.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr13:21732195 A>G maps to NM_145061.5 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr16:863366 C>T maps to NM_001013638.1 R239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr17:3977516 C>T maps to NM_015113.3 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr19:36631957 C>G maps to NM_001749.2 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr19:55993789 A>G maps to NM_033113.2 E406E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr2:234637942 G>A maps to NM_019093.2 Q57Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr20:43940943 C>T maps to NM_014276.2 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr3:122102041 A>G maps to NM_001017928.2 C10C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr5:79032747 T>C maps to NM_153610.3 T2720T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:45120713 G>T maps to NM_024587.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:168168188 G>A maps to NM_152902.3 T215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr1:175914296 A>G maps to NM_022457.5 L730L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr12:9223128 C>A maps to NM_000014.4 V1383V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr12:120582189 G>T maps to NM_006836.1 I1805I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr15:50835959 G>A maps to ENST00000456636 A102A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:23540827 C>T maps to NM_001083614.1 V449V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:31089678 T>C maps to NM_014699.3 A678A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:31195323 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr16:88765420 C>A maps to NM_178841.3 V166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr17:37579983 A>T maps to NM_004774.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr17:74288034 G>A maps to NM_032134.1 Q759*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr19:1466504 C>A maps to NM_005883.2 R1069R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:128918713 C>A maps to NM_020120.3 I899I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:153471510 T>A maps to NM_052905.3 S403S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:157367410 C>T maps to NM_000408.4 I126I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr2:179575503 G>A maps to NM_133378.4 G8196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr20:32880314 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr3:127358266 G>T maps to NM_015720.2 E84*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr4:164050120 G>A maps to NM_138386.2 P471P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr5:132084159 C>A maps to NM_001039780.2 S184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr5:140563806 C>A maps to NM_020957.1 S558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:36445952 T>C maps to NM_018685.2 N217N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:100681164 T>C maps to NM_001040105.1 Y2156Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr7:121651530 C>T maps to NM_002851.2 L811L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr8:130883631 C>A maps to NM_016623.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr1:154294467 C>T maps to NM_080429.2 F55F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr11:984671 C>T maps to ENST00000332231 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr11:62592561 C>A maps to NM_003164.3 E209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr11:126201298 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr12:57036239 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr15:44109599 T>G maps to NM_005926.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr21:36042940 C>T maps to ENST00000360731 A418A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr3:40465426 T>A maps to NM_001248.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr3:46492032 A>G maps to NM_002343.3 S278S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr3:147109012 C>A maps to NM_001168379.1 E275*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr4:123264652 C>G maps to NM_015312.3 G4147G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr7:92763421 G>A maps to NM_152703.2 I621I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr1:32100868 T>C maps to NM_012392.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr1:46032693 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr1:53555557 G>A maps to NM_006671.4 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr10:95400271 G>A maps to NM_006204.3 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr11:74085549 G>A maps to NM_173582.3 C63C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr12:56630208 C>G maps to NM_001135195.1 L325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr12:56742946 C>T maps to NM_005419.3 Q480Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr13:49796386 C>G maps to NM_001507.1 L371L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr14:20925020 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr16:2122848 G>A did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr16:3598163 T>C maps to ENST00000448023 L960L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:39261741 C>T maps to NM_001146041.1 C34C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:48559511 C>A maps to NM_018346.1 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:77915894 C>A maps to NM_019020.2 L673L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr17:79220315 C>T maps to NM_001037984.1 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr2:39285903 C>T maps to NM_005633.3 W85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr2:160086334 C>A maps to NM_033394.2 P1466P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr20:50769884 C>T maps to NM_018197.2 S282S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr21:34799206 A>T maps to ENST00000381995 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr22:40813488 G>A maps to NM_020831.3 S691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr3:46725270 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr5:160753380 C>G maps to NM_021911.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr7:27169875 C>A maps to NM_002141.4 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr7:92019369 T>C maps to NM_019004.1 Y664Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr8:87226721 T>A maps to NM_138817.2 R445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr8:144810121 G>A maps to NM_198488.3 D503D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5884-01A-11D-1589-08 chr9:35062135 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:36915922 C>T maps to ENST00000356637 E16E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:46751889 T>G maps to ENST00000254454 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:150804345 A>G maps to NM_001668.3 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr1:240256170 G>A maps to ENST00000406993 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:1027278 G>A maps to NM_005961.2 N740N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:66260241 G>A maps to NM_005700.3 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:75509460 C>T maps to NM_032564.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr11:124310918 C>T maps to NM_012378.1 P21P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr12:53931333 A>T maps to NM_001130059.1 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr13:29001982 G>A maps to NM_002019.4 D394D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr13:111885552 G>A maps to NM_001113511.1 E245E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr16:27374875 C>T maps to NM_000418.2 Q735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr17:4619902 C>A maps to ENST00000412477 T119T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr17:39658759 G>A maps to NM_153490.2 I370I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr17:59544912 G>C maps to ENST00000393853 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:27440796 C>A maps to NM_004341.3 Y45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:39526943 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:73680676 T>C maps to NM_015120.4 N2340N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:101670696 G>A maps to NM_001102426.1 F153F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr2:225422515 G>A maps to NM_003590.3 Q42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr20:57613689 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr22:39482534 C>G maps to NM_021822.3 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr22:41621937 G>A maps to NM_031488.4 P499P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr22:50987533 T>C maps to NM_138433.3 P313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr3:10387741 G>A maps to NM_001001331.2 L828L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr3:46009967 C>T maps to NM_024513.2 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:76877178 C>T maps to NM_018115.2 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:125592786 A>G maps to NM_020337.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:151829519 G>A maps to NM_006726.3 Q487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr5:66478707 T>G maps to NM_005582.2 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr6:32188965 G>A maps to NM_004557.3 N196N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:27856086 T>C maps to ENST00000409980 N652N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:91631867 A>G maps to NM_005751.4 E879E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:92119226 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr7:141759732 A>G maps to ENST00000475668 K1342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:17401958 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:25715867 G>A maps to NM_022659.2 L499L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:48826504 G>A maps to NM_006904.6 R913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr8:71126195 A>C maps to NM_006540.2 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr1:26671978 A>T maps to NM_001039775.3 P390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr1:103428307 G>A maps to NM_080629.2 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr11:66636399 C>A maps to NM_022172.2 L313L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr12:49431829 A>T maps to NM_003482.3 A3103A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr16:31371299 G>A maps to NM_000887.3 R207R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr17:26948414 A>G did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr19:3179455 C>T maps to NM_003775.3 L222L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr2:170072852 A>G maps to NM_004525.2 T1912T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr22:29627007 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr3:127379563 A>G maps to NM_015720.2 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr3:127396050 C>A maps to NM_172027.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr4:100787279 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr5:140481177 T>C maps to NM_018937.2 Y315Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr6:43226955 C>G maps to NM_032538.1 V399V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr6:106960431 C>G maps to NM_001624.2 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr6:121576520 T>A maps to ENST00000275159 V657V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr7:122269334 A>G maps to NM_001167940.1 D278D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr8:54764572 T>C maps to NM_170587.2 I38I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr9:4662476 C>A maps to NM_203453.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chrX:44949020 G>A maps to NM_021140.2 W1194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chrX:129201250 A>G maps to NM_001127197.1 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr1:247751787 T>C maps to NM_001001915.1 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr12:111923515 C>A did not map to a codon.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr13:110827562 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr15:33954437 C>T maps to NM_001036.3 C1569C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr17:18149934 G>A maps to NM_002018.2 F1008F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr19:13988493 A>G maps to NM_001098622.1 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr19:55452314 C>T maps to ENST00000446217 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr3:9989479 G>C maps to NM_207351.3 R459R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr4:76439475 T>C maps to NM_015436.2 E7E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr1:22190694 G>A maps to NM_005529.5 P1546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr1:204379182 C>A maps to NM_032833.3 E453*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr12:113704161 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr15:64426981 G>A maps to NM_003099.3 Q447Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr16:21611191 C>G maps to NM_016025.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr16:89345491 G>A maps to NM_013275.4 L2486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr17:33679779 G>A maps to NM_152270.3 A767A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr17:39191010 G>C maps to NM_030966.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr18:8379244 G>A maps to NM_001105244.1 R1231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:841047 C>T maps to NM_002777.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:5897009 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:49703679 G>T maps to NM_017636.3 V923V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr19:58991384 G>A maps to NM_017908.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr21:43298958 C>G maps to NM_022115.3 P86P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr5:158158100 A>G maps to NM_024007.3 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chr7:121681009 G>A maps to NM_002851.2 V1926V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chrX:50350697 C>T maps to NM_020717.3 E1148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5888-01A-11D-1589-08 chrX:107978242 C>T maps to NM_003604.2 R444R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:12089879 C>T maps to NM_021933.2 T258T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:158912062 T>G maps to NM_152501.3 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:238053764 A>T maps to NM_021186.3 A57A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr1:248458379 G>A maps to NM_001004692.1 C167C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr10:43312104 A>G maps to NM_014753.3 S796S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr10:81146145 G>A maps to NM_153367.3 C227C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:1093115 C>T maps to ENST00000441003 T1645T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr11:65480306 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr12:7362623 T>G maps to NM_001131023.1 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr12:75436983 G>T maps to NM_139137.2 G606G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr13:20398871 T>C maps to NM_001142684.1 K585K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr14:24032630 A>T maps to NM_003917.2 S456S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr16:624547 C>T maps to NM_148920.1 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr19:11312612 G>A maps to ENST00000319867 H1882H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr19:43773526 C>A maps to NM_002784.3 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr2:36583677 C>G maps to NM_016441.2 Y81*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr2:99978206 A>T maps to NM_015904.3 V281V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr2:113404572 A>G maps to NM_005415.3 V56V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr3:99648840 A>G maps to NM_001042459.1 A95A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr3:111432756 C>T maps to ENST00000312791 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr5:141033933 T>C maps to NM_022481.5 P1406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr6:117241540 T>C maps to NM_173560.3 D417D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr7:142562310 G>T maps to NM_004445.3 G251G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr9:136216908 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chrX:48751201 T>C maps to NM_001167947.1 T187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chrX:101910682 G>C maps to NM_001184727.1 G614G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chrX:154157882 C>T maps to NM_000132.3 T1394T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr1:2540841 C>T maps to NM_033467.3 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr1:201781617 G>T maps to ENST00000367296 E1684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr10:63699985 A>G maps to NM_032199.2 E107E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr10:96443671 C>A maps to NM_000772.2 G32G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr10:124351861 C>A maps to ENST00000368915 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr11:1092794 T>A maps to ENST00000441003 T1538T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr11:1093253 C>T maps to ENST00000441003 T1691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr11:67265786 G>A maps to NM_004910.2 S497S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr13:25352541 T>C maps to ENST00000381927 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:23083423 G>T maps to NM_020718.3 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:56792501 T>C maps to NM_014669.3 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr16:89294016 C>T maps to NM_182531.2 R413*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr17:7755371 T>G maps to NM_001080424.1 A1423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr17:66981099 G>A maps to NM_080283.3 I1435I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr19:39906056 G>T maps to NM_022835.2 E153*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr2:215880303 G>T maps to NM_173076.2 C622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr20:62642771 G>C maps to NM_012469.3 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:12192766 C>T maps to NM_133625.3 L238L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:47032942 G>T maps to NM_015175.1 L230L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:47143046 T>C did not map to a codon.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:129324249 C>G maps to NM_015103.2 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr3:134080583 C>A maps to ENST00000514516 E507*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr5:72743506 G>A maps to NM_004472.2 L227L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr5:161281259 G>A maps to NM_001127648.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr6:35213119 G>A maps to ENST00000394681 K855K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr6:51882413 G>A maps to NM_138694.3 F1798F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr9:69206733 C>T maps to NM_001085457.1 K317K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr9:113013694 T>C maps to NM_003329.2 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chrX:123200036 T>C maps to NM_001042750.1 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr1:61554263 T>C maps to NM_001145512.1 S202S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr1:93620446 T>A did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr12:14993940 C>T maps to NM_021071.2 W97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr12:57869642 G>T maps to ENST00000393797 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr12:104378525 G>T did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr12:112036796 C>T maps to NM_002973.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr13:22088515 C>T maps to NM_152726.2 V213V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr14:93813724 G>T maps to NM_182971.2 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr16:2168404 G>A maps to NM_001009944.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr16:67840334 C>T maps to NM_020850.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr18:43319598 G>A maps to NM_001146037.1 W362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr19:22605146 A>C did not map to a codon.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr20:23967128 C>T maps to NM_178311.2 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr20:43927152 G>A maps to ENST00000372754 F402F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr21:19685346 T>G maps to NM_002772.2 R694R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr22:19870862 A>T maps to NM_006440.3 I357I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr22:21989094 C>G maps to NM_152612.2 S248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr22:38051327 C>A maps to NM_018957.3 S581S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr3:8809675 G>A maps to NM_000916.3 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr3:46415325 C>T maps to NM_001100168.1 F311F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr4:140811128 T>C maps to ENST00000509479 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr4:174449978 C>T maps to NM_021973.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:136963989 G>A maps to NM_017415.2 N529N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:140711927 G>A maps to NM_018912.2 A559A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr5:174870045 G>A maps to NM_000794.3 D19D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr6:42657390 G>A maps to NM_015255.2 E1703E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr6:83862076 A>G maps to NM_015018.2 L2040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr8:95503872 T>C maps to NM_015496.3 S1691S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr9:136419612 C>T maps to ENST00000393061 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chrX:50350697 C>T maps to NM_020717.3 E1148E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chrX:107434728 T>C maps to NM_033641.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:43317093 C>A maps to ENST00000442768 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:60139805 G>C did not map to a codon.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr1:200973947 C>A maps to NM_017596.2 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr11:47819409 A>C maps to NM_015231.1 A1070A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr12:48866683 C>T maps to NM_012404.2 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:1673259 C>A maps to NM_002615.4 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:6597516 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:9846495 G>A maps to NM_201433.1 Q225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr17:73237523 G>T maps to NM_138619.2 V301V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr19:9085837 C>A maps to NM_024690.2 E1993*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr2:207827298 C>T maps to NM_173077.2 Y246Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr22:45574341 A>G maps to NM_007172.3 K188K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr4:68777128 C>T maps to NM_182606.3 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr5:63257392 G>A maps to NM_000524.2 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr5:70800507 C>T maps to NM_018429.2 Q768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chr6:25701538 T>C maps to NM_006998.3 C269C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5892-01A-11D-1589-08 chrX:129045743 C>T maps to NM_006649.3 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr11:1092965 C>A maps to ENST00000441003 T1595T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr11:113679908 G>T maps to NM_020886.2 Y680*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr11:117023229 C>A maps to NM_002572.3 R23R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr11:124095996 C>A maps to NM_001007249.1 L200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr15:65983019 C>T maps to ENST00000443035 V1304V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr15:75692464 C>T maps to NM_001145357.1 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr18:59888684 C>T maps to NM_020854.3 N271N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr19:34832920 G>A maps to NM_014686.3 L694L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr19:53762719 T>C maps to NM_173856.2 P364P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr4:79531259 A>T maps to NM_005139.2 G321G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr5:148730748 C>T maps to NM_152407.3 T194T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr6:29797246 C>T maps to ENST00000376828 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr6:147830099 G>A maps to NM_001030060.2 A12A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:59059733 C>T maps to NM_147189.2 S315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:67477039 T>A maps to NM_001080416.2 T717T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:113249530 G>T maps to NM_198123.1 Y3505*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:142186772 C>T maps to NM_014957.2 F793F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr8:144809116 G>C maps to NM_198488.3 A838A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr9:2110311 C>T maps to NM_003070.3 S1117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chr9:125391499 G>A maps to NM_001004450.1 F105F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chrX:41555434 T>A maps to NM_005300.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5893-01A-11D-1589-08 chrX:101908966 C>A maps to NM_001184727.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr1:109801210 G>C maps to NM_001408.2 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr11:1092812 C>T maps to ENST00000441003 T1544T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr13:61102843 T>C maps to NM_001146070.1 A495A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr16:56906658 A>G maps to NM_000339.2 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr17:72428209 C>G maps to NM_022036.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr19:48945879 T>C maps to NM_000836.2 A899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr20:10621488 C>A maps to NM_000214.2 S1047S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr6:47754338 C>A maps to ENST00000489301 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr7:121652843 T>C maps to NM_002851.2 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5894-01A-11D-1589-08 chr8:144940740 C>T maps to NM_031308.1 A2227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:6610657 C>A maps to NM_024654.4 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:10384006 C>A maps to ENST00000377086 P808P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:21889716 C>A maps to NM_000478.4 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:22161343 G>T maps to NM_005529.5 P3516P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:22216560 C>A maps to NM_005529.5 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:26127631 C>A maps to NM_020451.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:28800531 C>A maps to NM_023923.3 P440P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:32846846 G>T maps to NM_001143888.1 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:41232339 G>T maps to ENST00000308733 G265*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:45250839 C>A maps to NM_153274.2 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:47512253 G>T maps to NM_178033.1 G397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:60107001 C>A maps to NM_001113411.1 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:62979153 G>T maps to ENST00000371140 R1415R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:67438578 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:67861450 C>A maps to NM_001559.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:78444625 G>A maps to ENST00000436586 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:85418008 C>A maps to NM_153259.2 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:100680440 G>T maps to NM_001918.2 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:113658955 G>T maps to NM_014813.1 G860*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:117307104 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:150689612 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:150790506 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:156035748 C>A maps to NM_020387.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:156255157 C>A maps to NM_032323.2 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:157509097 C>A maps to NM_031281.2 G394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:161138358 G>T maps to NM_001122764.1 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:182856241 C>A maps to NM_001357.4 P1162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:233507887 C>A maps to NM_032435.2 R553R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr1:244724361 C>A maps to NM_001130957.1 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr10:45799336 C>A maps to NM_001004297.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr10:95372865 G>T maps to NM_006204.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr10:100453687 C>A maps to NM_021828.4 G325*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr10:112641151 C>A maps to NM_014456.4 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr10:118389556 C>A maps to NM_005396.4 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr10:129871606 C>A maps to NM_006504.4 R491R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:1275385 G>T maps to ENST00000447027 R5097R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:1275997 C>A maps to ENST00000447027 T5187T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:2424162 G>T maps to NM_005706.2 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:6807218 G>T maps to NM_001004489.2 *317Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:36296297 C>A maps to NM_014186.3 G161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:47308051 C>A maps to NM_003682.3 R874R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:47869464 C>A maps to NM_015231.1 A83A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:57175321 G>T maps to ENST00000428603 P486P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:61081071 G>T maps to NM_001923.3 P656P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:65386386 G>T maps to NM_032223.2 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:65396166 C>A maps to NM_032223.2 A1268A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:67210003 G>T maps to NM_020441.2 S32S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:82877252 C>A maps to NM_015885.3 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:85447591 C>A maps to NM_001162953.1 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:92896028 C>A maps to NM_152313.2 E294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:94301930 C>A maps to NM_152431.2 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:113205743 G>T maps to NM_017868.3 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:113268057 C>A maps to NM_178510.1 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:120976546 C>A maps to NM_005422.2 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:125867174 G>T maps to ENST00000392693 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:126073437 C>A maps to NM_032795.2 E337*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr11:129747249 C>A maps to NM_006165.3 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr12:18849162 G>T maps to ENST00000266505 T404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr12:24985764 G>T maps to NM_001178093.1 T324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr12:27835584 C>A maps to NM_003622.3 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr12:50392977 C>A maps to NM_013277.3 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr12:52799985 G>T maps to NM_033033.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr12:53454201 G>T maps to NM_170754.2 P877P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr12:57863447 C>A maps to NM_005269.2 R515R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr12:91502726 C>A maps to NM_002345.3 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr12:102590449 G>T maps to NM_002674.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr12:109609640 C>A maps to NM_001093.3 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr12:121618188 C>A maps to NM_002562.5 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr13:41766947 A>T maps to NM_032138.4 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr13:45563277 G>T maps to NM_012345.2 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr13:73482778 G>T maps to NM_006346.2 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr13:96282245 G>T maps to NM_198968.2 S269S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr13:99540612 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr13:99853734 G>T maps to NM_177967.3 G24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr14:21825489 C>A maps to NM_007192.3 L842L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr14:24526145 C>A maps to NM_138360.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr14:24588990 G>T maps to NM_025230.4 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr14:31614075 C>A maps to NM_015382.2 V856V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr14:35595980 C>A maps to NM_014672.2 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr14:65253750 C>A maps to ENST00000389723 E982*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr14:71064483 C>A maps to ENST00000430055 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr14:88450739 C>A maps to NM_000153.2 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr14:105175707 C>A maps to ENST00000252520 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:27777958 C>A maps to NM_033223.4 R446R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:28090199 T>A did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:31318400 C>A maps to NM_002420.4 R1168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:31818628 C>A maps to ENST00000382902 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:40921544 C>A maps to NM_170589.3 P1912P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:41795271 C>A maps to NM_002220.1 R432R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:42442668 C>A maps to ENST00000397272 E263*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:43016712 C>A maps to NM_138477.2 R1220R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:43748117 G>T maps to NM_001141980.1 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:45396347 G>T maps to NM_014080.4 V850V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:48548041 C>A maps to NM_000338.2 S659S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:55790461 G>T maps to NM_130810.2 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:62360004 C>A maps to NM_207322.2 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:64966234 G>T maps to NM_015042.1 G394G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:75091829 G>T maps to NM_004383.2 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:90610968 C>A maps to NM_198526.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:100801829 G>T maps to NM_139057.2 S295S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:100871169 G>A maps to NM_139057.2 I180I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr15:101933521 G>A maps to NM_002570.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:1719148 C>A maps to NM_020825.3 S1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:2030687 C>A maps to NM_172168.1 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:2156515 C>A maps to NM_001009944.2 E2458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:2988192 C>A maps to ENST00000399667 R645R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:3707936 G>T maps to NM_005223.3 E278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:9858736 C>A maps to NM_000833.3 T888T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:15188010 G>T maps to NM_018427.3 S27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:31288263 G>T maps to NM_001145808.1 V369V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:46618001 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:55360381 G>A maps to NM_024335.2 A60A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:68358713 C>A maps to NM_019023.2 A87A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:69373944 C>A maps to NM_016101.4 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:70866771 C>A maps to NM_032821.2 V4625V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:81390560 C>A maps to NM_022041.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr16:84215229 C>A maps to NM_005679.2 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:3397704 C>A maps to NM_000049.2 P232P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:3783691 C>A maps to ENST00000381771 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:4917021 C>A maps to NM_006612.5 V522V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:8021162 G>T maps to ENST00000380149 S205*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:12666457 C>A maps to NM_001146312.1 R820R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:19607398 C>A maps to NM_152908.3 S370S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:19845194 C>G maps to NM_007202.2 V335V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:30374835 C>A maps to ENST00000327564 R794R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:33348416 G>T maps to NM_001017368.1 P188P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:36873220 C>A maps to NM_005937.3 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:39341085 G>T maps to ENST00000398472 G7G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:43226775 C>A maps to NM_006460.2 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:44847308 G>T maps to NM_030753.3 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:47583739 G>T maps to NM_002507.3 S96S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:48625024 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:56603638 G>T maps to NM_004574.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:60637474 C>A maps to ENST00000326270 L273L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:71412055 C>A maps to NM_001144952.1 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:73504358 C>A maps to NM_020753.3 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:73664704 G>T maps to NM_013260.6 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:78071048 C>A maps to NM_017950.2 T1009T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:78078502 C>A maps to NM_001079804.1 R40R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:78293015 C>G maps to NM_020914.4 A1025A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:78897437 C>A maps to NM_020761.2 R925R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:79870324 G>A maps to NM_016538.2 C390C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:80046676 C>A maps to NM_004104.4 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr18:5969505 C>A maps to NM_173464.3 T509T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr18:13826276 G>T maps to NM_005913.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr18:28604399 G>T maps to NM_001941.3 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr18:28648895 C>A maps to ENST00000438199 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr18:28991185 C>A maps to NM_001134453.1 P729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr18:29046520 G>T maps to NM_001944.2 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr18:52609911 C>A maps to NM_025214.2 V37V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr18:54361933 G>T maps to NM_015285.2 G351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:327869 C>A maps to NM_017550.1 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:1796848 G>T maps to NM_138813.2 A538A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:4847807 C>A maps to NM_005817.4 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:6374897 C>A maps to NM_032306.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:16551693 A>G maps to ENST00000455140 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:18271293 C>A maps to NM_005027.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:18557589 G>A maps to NM_006532.3 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:19304835 C>A maps to NM_003721.2 P27P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:35556175 C>A maps to NM_182983.2 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:35828792 C>A maps to NM_001771.3 S285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:36044620 G>T maps to NM_000704.2 S864S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:39062837 C>A maps to NM_000540.2 P4642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:39589258 C>A maps to NM_001004318.2 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:40718850 C>A maps to NM_002446.3 T564T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:41931821 C>A maps to NM_198540.2 G288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:42729436 G>T maps to NM_133444.1 T294T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:46269286 G>T maps to NM_175875.4 T564T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BQ-7044-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:46998155 G>T maps to ENST00000377652 A89A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:48537495 C>A maps to NM_019855.3 G158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:49217245 C>A maps to NM_001130915.1 P260P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:50335224 C>A maps to NM_030973.3 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:51013673 C>A maps to NM_138334.2 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:55385757 C>T maps to NM_002000.2 Q5*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:55568057 G>T maps to NM_001145971.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr19:57060352 G>T maps to NM_020828.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:1915832 C>A maps to ENST00000399161 T556T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:27802750 C>A maps to NM_032266.3 P1104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:29093062 C>A maps to NM_017910.3 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:29093088 C>A maps to NM_017910.3 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:61433931 C>A maps to NM_014709.3 S3003S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:69734678 G>T maps to NM_014911.3 R680R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:73493808 C>A maps to ENST00000295133 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:75108949 C>A maps to NM_000189.4 A561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:112686877 C>A maps to NM_006343.2 P81P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:114512741 C>A maps to NM_025181.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:116066873 G>T maps to NM_020868.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:170606196 C>A maps to NM_144711.5 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:219885963 G>T maps to NM_194302.2 R1057R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:220494803 G>T maps to NM_201574.2 E208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr2:234360640 C>A maps to NM_152879.2 P733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr20:333867 G>T maps to NM_024958.2 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr20:3128491 C>A maps to NM_021826.4 G409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr20:19941402 C>A maps to ENST00000255006 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr20:20033244 G>T maps to NM_016652.4 G75G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr20:25261604 C>A maps to NM_002862.3 P420P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr20:30584914 C>A maps to NM_001011718.1 P465P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr20:45808506 C>A maps to ENST00000360649 L425L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr20:60895674 C>A maps to NM_005560.3 L2233L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr21:31971174 C>A maps to NM_181604.1 G7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr21:42861494 G>T maps to NM_001135099.1 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr21:45751855 C>A maps to ENST00000397956 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr22:18022099 C>A maps to ENST00000400579 P735P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr22:21098945 G>T maps to NM_058004.2 S1084S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr22:30210708 G>T maps to NM_032204.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr22:30776080 C>A maps to NM_001017981.1 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr22:31655114 G>T maps to NM_001031801.1 G66G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr22:36900701 G>T maps to NM_001102371.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr22:46776755 C>A maps to NM_014246.1 L2395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:9831254 C>A maps to NM_006354.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:9885221 C>A maps to NM_173659.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:9965959 C>A maps to NM_153461.2 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:49050902 G>T maps to NM_018031.3 E676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:49151632 G>T maps to ENST00000434032 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:49569638 C>A maps to NM_004393.4 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:50230724 G>T maps to NM_000172.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:52356490 G>T maps to ENST00000273600 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:52537075 C>A maps to NM_015136.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:53844186 C>A maps to NM_001128840.1 S2018S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:58094279 C>A maps to NM_001164317.1 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:93714738 G>T maps to NM_182896.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:123359179 C>A maps to NM_053025.3 T1597T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:126217015 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:130673863 C>T maps to NM_001001486.1 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:140406951 C>A maps to NM_152616.4 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:154021158 C>A maps to NM_020865.2 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:184290593 C>A maps to NM_004443.3 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:184689537 G>T maps to ENST00000437079 E1140*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr3:195497194 G>T maps to NM_018406.5 A4430A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr4:887707 C>A maps to NM_005255.2 S277S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr4:38828859 G>T maps to NM_006068.3 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr4:86985418 C>A maps to NM_138982.2 A370A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr4:100349064 G>T maps to NM_000673.4 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr4:128807323 C>A maps to NM_014264.4 R267R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr4:146560729 G>T maps to NM_172250.2 G147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr4:146695810 C>A maps to ENST00000508784 G903*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr4:154216703 C>A maps to NM_015271.3 L342L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:1034369 G>T maps to NM_033120.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:16701575 G>A maps to NM_012334.2 C976C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:32074079 C>A maps to NM_178140.2 L956L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:32108144 G>A maps to NM_178140.2 L2808L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:33938236 C>A maps to NM_016568.3 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:79752786 C>A maps to NM_014733.3 S1273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:122717833 G>T maps to NM_153223.3 R692R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BQ-7044-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:131007964 G>T maps to NM_133372.2 S724S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:137519792 C>A maps to NM_005733.2 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:156346470 G>T maps to NM_138379.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:171491788 G>T maps to NM_005990.3 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr5:179192886 G>A maps to NM_014757.4 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:7880268 G>T maps to NM_001718.4 G443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:27861392 C>A maps to NM_003527.4 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:30037034 C>A maps to NM_021959.2 P111P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:32014147 C>A maps to ENST00000375244 T3470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:33264471 G>T maps to NM_004761.3 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:36995879 G>T maps to NM_173558.3 E637*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:39859121 C>A maps to ENST00000398904 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:41657468 C>A maps to ENST00000343317 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:41753119 C>A maps to NM_013397.5 R142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:43013795 C>A maps to NM_001168370.1 S982S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:44121849 G>T maps to NM_018426.1 L717L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:55935545 G>T maps to NM_030820.3 L672L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:84649773 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr6:128297927 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:2611886 C>A maps to NM_152558.3 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:11068425 C>A maps to ENST00000303905 S479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:18767324 C>A maps to NM_178425.2 A618A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:56049936 C>A maps to NM_001483.1 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:56088776 C>A maps to NM_004577.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:73752799 A>T maps to NM_003388.4 S48S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:89874821 G>T maps to NM_001039706.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:102079481 C>A maps to NM_032831.2 R27R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:122526103 C>A maps to NM_001167940.1 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:123594289 G>T maps to NM_001174046.1 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:128040476 C>A maps to NM_000883.3 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:129767257 C>A maps to NM_014997.3 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr7:157414138 G>A maps to NM_002847.3 C753C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:9605676 C>A maps to NM_003747.2 P929P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:17868856 G>T maps to NM_006197.3 G1778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:20107304 G>A maps to NM_021020.2 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:21860740 G>T maps to ENST00000434536 T994T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:21958399 C>A maps to NM_022749.5 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:21958989 C>A maps to NM_022749.5 A552A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:28635399 G>T maps to NM_018250.3 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:38110632 G>T maps to NM_001164232.1 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:42565549 G>T maps to NM_000749.3 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:70667868 C>A maps to NM_030958.2 G350*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:98736855 C>A maps to NM_178812.3 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:102661726 G>T maps to NM_024915.3 A566A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:103309792 C>A maps to NM_015902.4 G1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:110451258 G>A maps to ENST00000426474 K1298K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:125528003 G>T maps to NM_032026.3 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:126095473 C>A maps to ENST00000377985 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:142176396 C>A maps to NM_014957.2 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr8:146107240 C>A maps to NM_021061.3 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr9:19296235 C>A maps to NM_017925.4 P108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr9:32987574 G>T maps to NM_001195248.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr9:94487128 C>A maps to NM_004560.2 L549L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr9:113562827 C>A maps to ENST00000189978 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr9:133342122 C>A maps to NM_000050.4 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr9:135781407 G>T maps to NM_000368.4 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr9:135929855 C>A maps to NM_001122823.1 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr9:136217856 G>T maps to NM_000972.2 S209S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr9:136536662 C>A maps to NM_007101.3 E774*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr9:140007893 C>A maps to NM_013379.2 A180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:37312612 C>A maps to NM_000950.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:38182772 C>A maps to NM_001034853.1 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:39913187 C>A maps to NM_001123385.1 E1643*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:48839465 C>A maps to NM_020137.3 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:48978845 C>A maps to NM_015698.4 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:50051760 G>T maps to NM_033031.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:54570662 C>A maps to NM_019067.5 V178V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:63551512 C>A maps to NM_017677.3 E426*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:71932673 G>T maps to ENST00000373539 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:75648748 C>A maps to NM_020932.2 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:76711902 C>A maps to NM_003868.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:96185819 C>A maps to NM_006729.4 S356*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:110951419 C>A maps to NM_001099922.2 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:115576125 G>T maps to NM_007231.3 G233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:117770315 C>A maps to ENST00000276204 L1298L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:130411039 C>A maps to NM_001170961.1 P832P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:135767982 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:151092924 C>A maps to ENST00000427663 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:153175668 G>T maps to NM_001164741.1 P744P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chrX:153593562 G>T maps to NM_001110556.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:43649506 C>A maps to NM_001195831.1 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:70895505 T>C maps to NM_001902.5 S206S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:94528185 A>T maps to NM_000350.2 A628A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:151112137 T>C maps to NM_001178061.1 E91E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr12:86272344 G>T maps to NM_006183.3 E120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr13:30096466 C>T maps to NM_003045.4 S392S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr14:20345256 C>A maps to NM_001005501.1 I277I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr14:35062275 A>T maps to NM_152233.2 S243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr14:38724315 C>T maps to NM_175060.1 R304R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr15:42536248 G>T maps to ENST00000389834 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr16:2052643 C>T maps to ENST00000431526 G185G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr16:3554720 T>C maps to NM_015041.1 N8N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr16:89613083 G>T maps to NM_003119.2 E490*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr17:4910622 C>A maps to NM_006612.5 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr17:27893330 C>A maps to NM_198147.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr17:42089523 C>T maps to NM_032376.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr17:61623122 C>T maps to NM_030779.2 L949L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr18:9257290 T>C maps to NM_015208.3 T1342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr18:31263417 A>G maps to NM_030632.1 G255G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr18:44635156 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr19:12759090 G>T maps to NM_000528.3 A854A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr19:35617293 G>T maps to NM_139284.2 T393T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr20:50405585 G>A maps to NM_020436.3 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr21:44317077 T>C maps to NM_021075.3 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr22:36661664 C>T maps to NM_145343.2 N277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr3:46939562 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr4:38990525 G>T maps to NM_024943.1 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr4:109571837 C>T maps to ENST00000512478 F9F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr5:122940482 C>A maps to NM_001044723.1 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr5:147010973 A>G did not map to a codon.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr6:2623683 C>A maps to NM_152554.2 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr6:155577963 C>A maps to ENST00000456144 P1634P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr6:168276026 A>C maps to ENST00000400822 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr7:82532015 A>G maps to NM_033026.5 P4493P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr7:100160552 C>T maps to NM_006076.4 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr8:118184886 C>A maps to NM_173851.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:119202961 G>T maps to ENST00000313400 V1236V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:130476384 C>T maps to NM_001002913.1 G213G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:131028576 G>A maps to NM_004486.4 Q197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:138839742 T>C maps to NM_016172.2 Q114Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr9:139418247 G>A maps to NM_017617.3 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chrX:48979104 G>T maps to NM_015698.4 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:1638913 G>T maps to NM_024011.2 P393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:5935028 G>A maps to NM_015102.2 A983A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:12336097 C>A maps to NM_015378.2 S818*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:29633652 C>A maps to ENST00000356870 R945R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:55534720 G>T maps to NM_015306.2 P2620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:111991340 G>T maps to NM_024102.2 A67A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:151509761 C>T maps to NM_020770.2 Y1184Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:161173307 C>A maps to NM_004550.4 A59A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:201034980 G>T maps to NM_000069.2 G946G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:205138903 C>A maps to NM_015375.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:237865330 G>T maps to NM_001035.2 G3141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr1:245850635 G>T maps to NM_018012.3 E1451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr10:131646670 G>T maps to ENST00000355311 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr10:135025295 C>A maps to ENST00000368572 A1392A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr11:47356601 C>A maps to ENST00000399249 E966*. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr11:48285841 G>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr11:55136282 C>A maps to NM_001005275.1 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr11:62571273 G>T maps to NM_006362.4 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr11:67269518 C>A maps to NM_004910.2 E152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr11:124765530 G>A maps to NM_019055.5 T286T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:12332915 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:14664538 G>T maps to NM_024829.5 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:56531437 C>A maps to NM_001184796.1 P708P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:104359838 G>C did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:113812292 C>A maps to NM_173542.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:120150414 G>C maps to ENST00000392521 L1555L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:123425508 C>A maps to NM_203444.2 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr12:129285554 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr14:20851789 C>A maps to NM_007110.4 E1242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr14:60619791 C>A maps to NM_016029.2 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr15:22999550 C>A maps to NM_014608.2 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr15:49135785 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr15:63012060 C>A maps to NM_015059.2 S991S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr15:101454974 C>A maps to NM_000693.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr16:31075435 G>T maps to NM_001172669.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr16:57689339 G>T maps to NM_005682.5 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr17:4451583 C>T maps to NM_001105538.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr17:7476180 C>A maps to NM_001416.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr17:72436052 T>A maps to NM_022036.2 S91S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr19:3525915 G>A maps to NM_001136198.1 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr19:6177403 C>A maps to NM_030924.3 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr19:17412416 G>T maps to NM_024527.4 T3T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr19:18183033 C>A maps to NM_005535.1 L303L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr19:19656281 G>T maps to NM_153221.2 R976R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr19:34884660 G>T maps to NM_000175.3 S298S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr19:47856335 C>A maps to NM_014681.5 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr19:54483199 C>A maps to NM_031895.5 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr2:24261377 G>C maps to NM_025203.2 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr2:233246205 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr20:33530309 G>T maps to NM_000178.2 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr20:33623037 C>A maps to NM_015638.2 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr20:45702813 C>A maps to ENST00000360649 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr20:60581802 G>T maps to NM_003185.3 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr21:37444951 C>A maps to NM_001757.2 T202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr21:47410320 G>T maps to NM_001848.2 G329G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr22:22049727 C>A maps to NM_148175.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr22:36692896 G>T maps to NM_002473.4 A1088A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr3:46785491 G>T maps to ENST00000331814 A84A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr3:53894169 G>T maps to NM_018725.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr3:64527078 C>A maps to NM_182920.1 A1768A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr3:143214263 C>A maps to NM_173653.3 A372A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr3:183994321 C>A maps to NM_001100120.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr5:156314 G>T maps to NM_052909.3 E424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr5:13727613 A>G did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr5:32088329 G>T maps to NM_178140.2 S1592S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr5:145862221 C>A maps to NM_006706.3 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr5:149636394 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr5:169680127 C>A maps to NM_005565.3 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr5:179554620 C>A maps to NM_175062.3 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr6:29408019 G>T maps to NM_013941.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr6:30679684 C>A maps to NM_014641.2 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr6:31323370 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr6:169646334 C>A maps to NM_003247.2 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr7:21737743 A>G maps to NM_003777.3 L2038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr7:89854722 G>T maps to NM_152999.3 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr7:102098230 G>T maps to NM_017621.3 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr7:107613453 C>A maps to NM_002291.2 G515G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr8:37697782 C>A maps to NM_032777.9 R886R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr8:104080962 G>T maps to NM_001695.4 L379L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chrX:47775367 C>A maps to NM_007137.3 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:11737605 C>A maps to ENST00000376669 L75L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:16055188 G>T maps to ENST00000420314 V752V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:26629409 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:27428247 G>T maps to NM_003047.3 R669R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:36809736 C>A maps to ENST00000373130 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:45807619 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:47834268 C>A maps to NM_016308.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:112998998 C>A maps to NM_018704.2 T295T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:117633171 A>T maps to NM_003594.3 K839*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:169824949 A>T maps to NM_181093.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:185931710 C>A maps to NM_031935.2 S630S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:186266027 C>A maps to NM_005807.3 P7P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:186324771 T>A maps to NM_003292.2 K673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr1:211924302 C>A maps to NM_014873.2 G321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:323441 C>A maps to NM_014974.2 L1498L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:81702147 G>C maps to NM_003019.4 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:94821055 G>T maps to NM_183374.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:97371148 G>T maps to NM_002860.3 P658P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:98945278 C>A maps to NM_003061.2 G51G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:99527408 C>A maps to NM_003015.3 V272V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:104679505 C>A maps to NM_017649.3 P423P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:104866416 C>A maps to NM_001134373.1 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:111878342 A>G did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:120354267 C>A maps to NM_004248.2 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr10:131973331 G>T maps to NM_006541.4 V312V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:2424126 C>A maps to NM_005706.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:12020307 C>A maps to ENST00000450094 G124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:12316189 C>T maps to NM_032867.2 D404D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:17539021 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:55433370 G>T maps to NM_001004704.1 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:60540954 C>A maps to NM_001098835.1 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:82879695 C>A maps to NM_015885.3 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:89956062 G>T maps to NM_012124.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:118498255 C>A maps to NM_015157.2 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:119210070 G>C maps to NM_015645.3 S234S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:124180242 G>T maps to NM_001002917.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:125848278 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:12302075 C>T maps to NM_002336.2 V1002V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:19512455 C>A maps to ENST00000429027 P1148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:48377923 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:48888592 T>C maps to NM_152319.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:54675613 C>A maps to NM_031157.2 G56G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:54803345 C>A maps to NM_002205.2 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:70704757 C>T maps to NM_014515.5 Y44Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:108091331 C>A maps to NM_007062.1 L234L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:111886057 C>A maps to NM_005475.2 S560S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr12:130929756 C>A maps to NM_015347.4 A196A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr13:29855997 C>A maps to NM_001033602.2 P944P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr13:99947321 C>A maps to NM_004951.4 G360*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:20853154 G>T maps to NM_007110.4 S1032S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:24686352 C>A maps to NM_006156.2 G76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:35872503 A>G maps to NM_020529.2 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:64593130 G>T maps to NM_182914.2 V4547V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:65208368 C>A maps to ENST00000394691 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:75330069 G>T maps to ENST00000445876 P156P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:75367771 C>A maps to NM_001933.4 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:77793879 C>A maps to NM_145870.2 I67I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:94394720 C>A maps to NM_138344.3 P92P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr14:105843142 C>A maps to ENST00000458164 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:28421671 G>T maps to NM_004667.4 P3196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:33795866 G>T maps to NM_001036.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:34102697 G>T maps to NM_001036.3 E3349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:42109814 G>T maps to NM_001128608.1 G602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:48756162 G>T maps to NM_000138.4 T1666T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:49255029 G>T maps to NM_203349.3 P61P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:51750977 C>A maps to NM_001174116.1 L2647L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:55789913 C>A maps to NM_130810.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:69548654 C>A maps to NM_015554.1 P170P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:81282036 G>A maps to NM_015154.1 C32C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:90281299 C>A maps to NM_020212.1 T598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:90349637 G>T maps to NM_001150.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr15:101567474 C>A maps to NM_024652.3 S805S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr16:3306533 G>T maps to NM_000243.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr16:4730037 C>A maps to NM_015246.2 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr16:30507521 G>T maps to NM_002209.2 L536L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr16:30768823 C>A maps to NM_001014979.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr16:31422759 G>T maps to ENST00000444228 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr16:67188622 C>A maps to NM_003789.3 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr16:84228054 C>A maps to NM_139174.3 C214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr16:88874554 G>T maps to NM_030928.3 E504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:1538054 G>T maps to NM_003693.2 P830P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:17769715 G>T maps to NM_001082968.1 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:25932701 G>T maps to ENST00000268763 L564L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:26854267 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:41939230 C>A maps to NM_145273.3 L317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:42476315 C>A maps to NM_001002909.2 R1043R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:56565508 G>A maps to NM_001080439.1 Q43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:61562732 G>T maps to NM_000789.3 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:72281208 C>A maps to NM_023036.4 R72R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:72368138 C>A maps to ENST00000440684 P1226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:74158076 C>A maps to NM_052916.2 E267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:77709029 G>T maps to NM_178543.3 G196G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:78169446 G>T maps to NM_024110.2 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr17:80130669 G>T maps to ENST00000445854 R525R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr18:21703897 G>T maps to NM_001135993.1 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr18:54424319 C>A maps to NM_015285.2 T832T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:1047217 G>T maps to NM_019112.3 A636A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:1080532 C>A maps to NM_012292.2 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:9525012 G>T maps to NM_006631.2 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:18332979 G>T maps to NM_000923.3 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:19656327 G>T maps to NM_153221.2 E992*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:39086627 G>T maps to NM_001042600.1 P710P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:41312518 C>A maps to NM_053046.2 P301P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:46289910 C>A maps to NM_004943.1 A281A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:54848914 G>T maps to NM_012276.3 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:55453036 C>A maps to ENST00000446217 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:57133474 G>T maps to NM_021216.4 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr19:57911025 C>A maps to NM_001172773.1 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:24985566 C>A maps to NM_003743.4 P1359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:37247815 C>A maps to NM_019024.1 L1339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:48869595 G>T maps to NM_172311.2 L805L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:70315542 C>A maps to NM_006196.3 S223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:71896869 C>A maps to NM_001130987.1 A1926A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:74328199 G>T maps to ENST00000409262 G1336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:97009945 C>A maps to NM_015341.3 S233S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:98275420 G>T maps to NM_005735.3 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:109100750 C>A maps to NM_181453.3 T1199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:122122689 C>A maps to NM_015282.2 E1353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:128526505 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:153417434 C>A maps to NM_052905.3 S161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:178977554 C>T maps to ENST00000456670 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:220422725 G>T maps to NM_015311.2 P1203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr20:30784401 G>T maps to NM_002657.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr21:31709824 G>A maps to NM_001077711.1 C54C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr21:32638550 G>A maps to NM_003253.2 N246N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr21:34923024 G>T maps to NM_138927.1 A496A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr21:35821908 C>A maps to NM_000219.3 A8A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr21:46276238 C>A maps to NM_004339.2 G106G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr21:46898248 C>A maps to ENST00000359759 P825P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr22:17280835 G>T maps to NM_175878.3 I138I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr22:18003266 G>T maps to ENST00000400579 E319*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr22:21335279 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr22:30198152 C>A maps to NM_032204.3 V466V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr22:38467749 G>T maps to NM_012407.3 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr22:44581730 C>A maps to NM_001137606.1 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr22:50716685 C>A maps to NM_012401.2 E1583*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:9517351 C>A maps to ENST00000407969 P1321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:10084322 C>A maps to NM_033084.3 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:38913196 C>A maps to ENST00000302328 V1166V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:42264622 C>A maps to NM_001042646.1 A752A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:48618340 C>A maps to NM_000094.3 G1652*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:52524847 G>T maps to NM_007184.3 T1247T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:53259872 G>T maps to ENST00000423516 R599R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:107435612 C>A maps to NM_001142568.1 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:140997283 C>A maps to NM_001037172.1 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:171394618 G>A maps to NM_002662.3 F667F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr3:189705317 C>A maps to NM_018192.3 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr4:3237927 C>A maps to NM_002111.6 P2946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr4:77675775 C>A maps to NM_020859.3 P1380P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr4:154214210 C>A maps to NM_015271.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr4:158224863 C>A maps to NM_000826.3 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr4:185724471 A>T did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr4:187159475 G>T maps to ENST00000511608 V232V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr5:353871 C>A maps to NM_020731.3 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr5:11117618 C>A maps to NM_001332.2 T740T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr5:41917335 G>T maps to NM_175921.4 E274*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr5:140041203 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr5:145862221 C>A maps to NM_006706.3 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr5:176078874 C>A maps to NM_012171.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:4037654 C>A maps to NM_003913.4 L421L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:10927480 G>T maps to NM_001040274.2 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:31850771 G>T maps to ENST00000395728 L1060L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:42585063 C>A maps to NM_015255.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:43498443 G>T maps to NM_020750.2 R887R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:43541218 G>C maps to NM_020750.2 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:44390389 T>C maps to NM_001253.2 P416P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:144869981 C>A maps to NM_007124.2 R2268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:150005369 G>T maps to NM_004690.2 I285I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:152201892 A>G maps to NM_001122741.1 G249G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr6:154521108 C>G maps to NM_001130700.1 L201L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr7:5553289 C>A maps to ENST00000312577 E6*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr7:73249098 C>A maps to NM_152559.2 G238*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr7:130023239 G>T maps to NM_001868.2 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr7:149559029 G>T maps to NM_001099220.1 T927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr7:154738450 C>A maps to NM_007349.3 G999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr7:155090372 C>A maps to ENST00000344756 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr8:22081814 C>A maps to NM_014759.3 E128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr8:22969259 C>A maps to ENST00000356864 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr8:95704907 C>A maps to NM_017697.3 P608P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr8:125326241 C>A maps to NM_194291.2 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr8:135614686 G>T maps to NM_020863.3 V425V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr8:144696826 G>T maps to NM_003313.3 S144*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr9:34372143 G>T maps to NM_020702.3 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr9:71843017 G>T maps to NM_004817.3 E481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr9:77473642 C>A maps to NM_017662.4 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr9:117120447 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr9:131899916 G>T maps to NM_178001.2 V279V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr9:134004847 G>T maps to ENST00000451030 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr9:134398372 C>A maps to NM_007171.3 S708S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr9:138651569 C>A maps to ENST00000298480 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chrX:22231073 C>A maps to NM_000444.4 R567R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chrX:26157311 C>A maps to NM_173699.3 T70T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chrX:40450511 G>T maps to NM_005765.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chrX:55028714 C>A maps to NM_014481.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chrX:69508001 C>A maps to NM_016484.4 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chrX:153069982 G>T maps to ENST00000393758 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chrX:153070280 C>A maps to ENST00000393758 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:977519 C>A maps to NM_198576.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:2540856 C>A maps to NM_033467.3 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:5965708 C>A maps to NM_015102.2 V582V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:6680255 G>T maps to NM_153812.2 G179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:15772169 C>A maps to NM_007272.2 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:16736160 C>A maps to NM_198546.1 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:17318771 C>A maps to NM_022089.2 P657P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:24125443 C>A maps to NM_001008216.1 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:27120704 G>T maps to NM_017837.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:27219261 G>T maps to NM_022078.2 R378R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:28476938 G>T maps to NM_001164721.1 V198V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:41228642 C>A maps to ENST00000308733 A215A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:45140015 G>T maps to NM_024587.2 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:45291921 C>A maps to NM_003738.4 L1038L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:54640458 C>A maps to NM_001031672.2 E261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:55277855 C>A maps to NM_001110533.1 S252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:55567367 G>T maps to NM_015306.2 P1678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:65850000 C>A maps to ENST00000371069 S264S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:85648023 G>T maps to NM_032184.1 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:94342800 C>A maps to NM_014597.4 V230V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:109793849 C>A maps to NM_001408.2 A383A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:111216030 G>T maps to NM_002232.3 A467A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:114215982 C>A maps to NM_001142782.1 R1029R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:144877176 G>T maps to NM_014644.4 R1504R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:150997191 C>A maps to NM_021222.1 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:158725363 G>T maps to NM_001005184.1 L253L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:169519881 G>T maps to ENST00000367796 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:175054580 C>A maps to NM_022093.1 P425P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:228474493 C>A maps to NM_001098623.1 R3100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:230410189 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:245850523 C>A maps to NM_018012.3 T1413T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:247016442 C>A maps to ENST00000428671 E1543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:247062791 C>A maps to ENST00000428671 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr1:247607321 G>T maps to NM_004895.4 S906S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:1230950 C>A maps to NM_018702.2 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:12123549 C>A maps to NM_018706.5 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:21108409 C>A maps to ENST00000430741 P666P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:69926168 C>A maps to NM_032578.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:70412305 C>A maps to NM_030625.2 T1472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:73055597 G>T maps to NM_170744.3 G736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:73453979 G>T maps to ENST00000398860 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:74658701 C>A maps to NM_152635.1 L114L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:75530063 C>A maps to NM_198597.1 T963T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:90342064 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:96824688 C>A maps to NM_000770.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:98781170 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:99140659 C>A maps to NM_015179.3 E477*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:124043431 G>T maps to ENST00000368994 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:126523374 C>A maps to NM_032182.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:1316979 G>T maps to ENST00000382211 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:5173566 G>T maps to NM_012375.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:5988905 C>A maps to NM_001146033.1 P273P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:10523015 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:46568800 C>A maps to ENST00000458649 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:47828692 C>G did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:64022762 C>A maps to NM_000932.2 R149R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:64821985 G>T maps to ENST00000340252 S276S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:64953473 C>A maps to NM_005186.3 A181A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:67191522 C>A maps to NM_001166222.1 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:72552598 G>T maps to ENST00000409314 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:75316929 C>A maps to NM_033063.1 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:76371796 G>T maps to NM_001128922.1 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:82882882 A>G maps to NM_015885.3 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:95520787 C>A maps to NM_144664.4 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:108158367 G>T maps to NM_000051.3 V1345V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:117335787 C>A maps to NM_020693.2 T1105T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:119050551 C>A maps to NM_024618.2 R608R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:119051967 T>A did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:126162414 C>A maps to NM_148910.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:2019077 G>T maps to NM_172364.4 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:6964681 C>A maps to NM_001098536.1 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:12274334 G>T maps to NM_002336.2 R1523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:27149676 C>A maps to NM_016551.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:32902874 G>T maps to NM_001040436.1 R424R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:41967122 C>A maps to NM_001164595.1 R848R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:49425592 C>A maps to NM_003482.3 G4299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:50050188 C>A maps to NM_175736.4 E295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:56477655 G>T maps to NM_001982.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:56491619 C>A maps to NM_001982.2 R838R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:57502043 C>A maps to NM_003153.4 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:101693786 C>A maps to NM_014503.2 T541T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:105381984 C>A maps to NM_152318.2 S52S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:108104180 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:111746252 C>A maps to NM_015267.3 S394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:130926968 C>A maps to NM_015347.4 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr12:132682408 C>A maps to NM_001122636.1 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr13:21303283 G>T maps to NM_174928.1 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr13:25265129 C>A maps to NM_001185085.1 T276T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr13:41515247 G>T maps to NM_172373.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr13:46288305 C>A maps to NM_152719.1 T382T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr13:52997747 C>A maps to NM_016075.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr13:99481725 C>A maps to ENST00000428223 T1577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr13:103275271 C>A maps to ENST00000376052 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr13:110833683 C>A maps to NM_001845.4 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr13:111933011 G>T maps to NM_001113511.1 V592V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr13:113773072 G>T maps to NM_000131.3 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr14:74449812 G>T maps to NM_001249.2 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr14:86089366 G>T maps to NM_013231.4 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr14:103412004 G>T maps to NM_006035.3 R1269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr14:104027027 C>A maps to NM_001015049.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:28362204 G>T maps to NM_004667.4 P4456P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:39880826 C>A maps to NM_003246.2 P524P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:42143315 C>A maps to ENST00000320955 T3592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:43038413 G>T maps to ENST00000263802 S1510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:64067420 C>A maps to ENST00000261887 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:65983370 G>T maps to ENST00000443035 P1187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:73562520 C>A maps to NM_002499.3 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:78475046 C>A maps to NM_015162.4 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:79356856 C>A maps to NM_002891.4 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:83499371 C>A maps to NM_001080435.1 R555R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:101549265 C>A maps to NM_024652.3 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:426547 G>T maps to NM_021259.2 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:1263927 C>A maps to NM_021098.2 P1642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:14041766 C>A maps to NM_005236.2 R772R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:15494713 G>T maps to NM_001128423.1 L127L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:19126781 C>A maps to NM_001034841.3 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:22360667 C>A maps to NM_001802.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:29847043 C>A maps to NM_017458.3 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:30017652 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:30939822 G>T maps to NM_001099784.2 V241V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:57188357 G>T maps to NM_024946.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:58619387 G>T maps to NM_016284.3 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:66420798 G>T maps to NM_001795.3 G100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:66886613 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:67327780 G>T maps to NM_001100915.1 P628P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:75269034 C>A maps to NM_001170714.1 E634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:84228075 G>T maps to NM_139174.3 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:87936069 C>A maps to NM_001739.1 V172V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:88902641 C>A maps to NM_000512.4 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr16:89348520 G>T maps to NM_013275.4 R1477R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BQ-7049-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:6329947 G>T maps to NM_014336.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:8159685 C>A maps to NM_012393.2 S261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:8172151 C>A maps to NM_012393.2 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:10247204 G>T maps to NM_003802.2 P602P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BQ-7049-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:17415868 G>T maps to NM_148172.1 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:27075398 C>A maps to NM_004295.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:34416068 G>T maps to NM_002983.2 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:37113471 G>T maps to NM_001008777.2 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:38324636 C>G maps to NM_007359.4 P644P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:39767954 C>A maps to NM_005557.3 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:40659536 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:56356993 G>T maps to ENST00000340482 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:56388088 C>A maps to NM_004758.2 L1161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:71197420 C>A maps to NM_018714.2 S485S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:72736917 G>T maps to NM_001006638.2 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:74004369 G>T maps to NM_001988.2 S1639*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:76122886 G>T maps to NM_007267.6 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr17:80040426 C>A maps to NM_004104.4 V1965V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr18:12325447 C>A maps to NM_032525.1 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr18:21114472 C>A maps to NM_000271.4 T1176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr18:21395475 C>A maps to ENST00000416669 S664S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr18:34320645 G>T maps to NM_025135.2 E1027*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr18:35145484 C>A maps to NM_020180.3 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr18:47398599 C>A maps to NM_001080467.2 A1180A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr18:74154839 C>A maps to ENST00000443185 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:847815 C>A maps to NM_002777.3 P206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:4157209 C>A maps to NM_032607.1 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:4453968 G>T maps to NM_025241.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:6141559 T>C maps to NM_030924.3 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:6750600 C>A maps to ENST00000313244 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:9958727 G>T maps to NM_006221.2 S98S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:10381852 C>A maps to NM_000201.2 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:12791043 C>A maps to NM_001930.2 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:15754733 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:19030661 G>T maps to NM_019070.4 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:19380544 C>A maps to NM_001001524.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:31025863 C>A maps to NM_014717.1 R761R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:40929051 G>T maps to NM_013376.3 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:41286333 C>A maps to ENST00000419646 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:42510814 G>T maps to NM_002088.3 S673S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:46313907 G>T maps to NM_030785.3 R281R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:48734067 G>T maps to NM_001184900.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:49119185 C>A maps to NM_000979.2 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:50728876 C>A maps to NM_001145809.1 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:50752993 G>T maps to NM_001145809.1 E524*. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:52869311 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:54966716 C>A maps to ENST00000431846 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr19:55915799 C>A maps to NM_014501.2 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:20403756 G>T maps to NM_001006946.1 P148P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:26699044 G>T maps to NM_194248.2 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:97377600 C>A maps to NM_001142292.1 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:98709581 C>A maps to NM_144992.4 T9T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:127821182 C>A maps to NM_139343.1 A246A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:128378022 C>A maps to ENST00000389524 P1143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:128393304 C>A maps to ENST00000389524 P1918P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:152410485 G>T maps to NM_001164507.1 P6494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:152521923 C>A maps to NM_001164507.1 E1721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:160050973 G>T maps to NM_033394.2 L983L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:163031473 G>T maps to NM_004460.2 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:178482877 C>A maps to NM_152275.3 S184S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:189868135 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:204255839 C>A maps to ENST00000295851 P184P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:204304840 G>A maps to ENST00000374493 P1076P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:219300065 C>A maps to NM_007127.2 R579R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:219525947 G>T maps to NM_004328.4 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:234752910 C>A maps to NM_018410.3 G172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:238283361 C>A maps to NM_004369.3 A1124A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:242277177 G>C maps to ENST00000391972 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr20:1532595 G>T maps to ENST00000381621 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr20:18286991 G>T maps to ENST00000401790 E60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr20:30723908 A>G maps to NM_014742.3 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr20:30737519 C>A maps to NM_014742.3 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr20:41306548 C>A maps to ENST00000373198 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr21:38390296 C>A maps to NM_018962.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr21:43547922 C>A maps to NM_173568.3 P1352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr21:44179143 C>A maps to NM_002606.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr22:24582357 C>A maps to NM_019601.3 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr22:38471046 G>T maps to NM_012407.3 E386*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr22:50617375 C>A maps to NM_052839.3 P568P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:5022083 C>A maps to NM_003670.2 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:9760187 G>T maps to ENST00000383832 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:44683519 G>T maps to NM_006991.3 E300*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:46023121 G>T maps to NM_024513.2 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:46026359 G>T maps to NM_024513.2 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:52643971 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:64085133 G>T maps to NM_198859.3 R710R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:64527078 C>A maps to NM_182920.1 A1768A. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BQ-7049-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:98300251 G>T maps to ENST00000512905 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:100042451 G>T maps to ENST00000394144 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:102175066 G>T maps to NM_175056.1 G136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:130737434 G>T maps to ENST00000514044 T476T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:156241613 A>G did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:183681370 T>C maps to NM_005688.2 G679G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr3:195515734 G>T maps to NM_018406.5 R906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:3031084 C>A maps to NM_182982.2 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:39458116 G>T maps to NM_000661.4 P100P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:42895654 C>A maps to NM_001080476.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:57367855 C>A maps to NM_006947.3 A615A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:68359613 C>A maps to NM_001812.2 G760*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:81122481 C>A maps to NM_001099403.1 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:89427001 C>A maps to NM_016323.2 A1016A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:89660227 G>T maps to NM_014883.2 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:96762281 C>A maps to NM_005390.4 L327L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:152069124 C>A maps to NM_001009555.3 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:166006751 C>A maps to NM_001100389.1 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr4:169342916 G>T maps to NM_001012967.1 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr5:434294 C>A maps to NM_020731.3 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr5:52235436 C>A maps to NM_181501.1 P1032P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BQ-7049-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr5:139715602 C>A maps to NM_001945.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr5:149515316 C>A maps to NM_002609.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr5:154394891 G>T maps to NM_001099293.1 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr5:176895198 C>A maps to ENST00000393565 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr5:177683355 G>T maps to ENST00000390654 R294R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr6:29633971 G>T maps to NM_002433.4 A160A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr6:33646558 C>A maps to ENST00000374316 T1305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr6:35436771 C>A maps to NM_007104.4 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr6:36993626 C>A maps to NM_173558.3 P506P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr6:41126793 C>A maps to NM_018965.2 E165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr6:74210319 C>A maps to NM_001123226.1 P687P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr6:135751081 G>T maps to NM_017651.4 P810P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr6:149730785 C>A maps to NM_015093.4 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:18669039 C>A maps to NM_178425.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:20371502 C>A maps to NM_002214.2 S25*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:33573753 C>A maps to NM_198428.2 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:36459788 C>A maps to NM_018685.2 S627S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:47842924 C>A maps to NM_138295.3 R2615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:73474351 C>A maps to ENST00000358929 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:87808318 C>A maps to NM_021723.3 P790P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:99621916 C>A maps to NM_003439.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:107335067 G>T maps to NM_000441.1 S448S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:111462464 C>A maps to ENST00000428084 P961P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:128486367 G>T maps to NM_001458.4 V1326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:130148459 C>A maps to NM_012133.4 R260R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:131241028 G>C maps to NM_001018111.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr7:150695740 G>T maps to NM_000603.4 G263G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:12957325 C>A maps to NM_182643.2 T840T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:17849057 C>A maps to NM_006197.3 T1513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:22428724 C>A maps to NM_005775.4 P578P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:23167233 G>T maps to NM_002318.2 S609S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:23538946 C>A maps to NM_006167.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:42037494 G>A maps to NM_000930.3 L438L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:72129011 C>G maps to NM_000503.4 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:87447900 C>A maps to NM_007013.3 R573R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:87638273 C>A maps to NM_019098.4 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:102570793 C>A maps to NM_024915.3 P144P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:124369950 C>A maps to NM_014109.3 G470*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:133198358 C>A maps to NM_004519.2 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:144668460 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:145737311 G>T maps to ENST00000428558 P1125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:146067310 G>T maps to ENST00000446747 T283T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr8:146107820 G>T maps to NM_021061.3 P254P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:396900 G>T maps to NM_203447.3 S1029S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:4576649 C>A maps to NM_004170.5 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:33364757 G>T maps to NM_002504.4 E1009*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:34613786 C>A maps to NM_007234.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:36118827 G>T maps to NM_021111.2 S776S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:71606112 C>A maps to NM_003558.2 T520T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:73426085 C>A maps to ENST00000419692 G291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:95060597 C>A maps to NM_017948.5 G1132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:97869473 C>A maps to NM_000136.2 T469T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:117853222 G>T maps to NM_002160.2 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:119488092 G>T maps to ENST00000313400 P921P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:125424827 C>A maps to ENST00000373686 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:126429319 G>T maps to NM_020946.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:135276978 G>T maps to NM_007344.2 P410P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:136262420 G>T maps to NM_153710.3 E333*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:139325462 G>T maps to NM_019892.3 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:140001760 C>A maps to NM_016219.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr9:140441842 C>A maps to NM_001098537.1 T37T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:16773187 T>C maps to NM_032796.3 N232N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:38664674 C>A maps to NM_021242.4 S159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:44919370 C>A maps to NM_021140.2 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:46502738 G>T maps to NM_032591.1 L515L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:48771708 C>A maps to NM_006875.3 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:69510590 C>A maps to NM_012310.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:70464708 G>T maps to ENST00000373988 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:70601746 C>A maps to ENST00000449580 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:85403764 G>T maps to NM_053281.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:100655745 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:105879845 C>A maps to NM_018015.5 T459T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:129171340 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:153599289 C>A maps to NM_001110556.1 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chrX:153880441 G>T maps to NM_172377.3 P168P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr1:1458173 C>G maps to NM_018188.3 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr1:226109584 C>A maps to NM_013328.2 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr11:120769326 C>A maps to NM_014619.2 T417T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr12:56720459 T>C maps to NM_001127460.2 P401P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr12:72017887 A>T maps to NM_144982.4 L1501*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr13:100925448 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr14:88450848 C>A maps to NM_000153.2 L157L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr14:89338025 G>T maps to NM_144596.2 E395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr15:39882094 C>G maps to NM_003246.2 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr15:42280292 C>A maps to NM_001080490.1 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr19:39898402 T>C maps to NM_003407.2 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr2:105654587 C>A maps to NM_182640.2 S13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr7:116166676 C>T maps to NM_001753.4 D43D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr7:150878331 G>T maps to ENST00000422024 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7050-01A-11D-1961-08 chr8:18725515 C>A maps to ENST00000440756 T434T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:1269090 G>T maps to NM_152228.1 S602S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:26448528 C>A maps to NM_152835.3 R163R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:32256857 G>T maps to NM_144569.4 S999S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:42048584 A>T maps to NM_024503.3 L628L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:52902540 G>T maps to NM_001009881.2 R1350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:77510218 C>A maps to NM_030965.1 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:214556992 G>A maps to NM_005401.4 A735A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr1:226065225 C>A maps to NM_014698.2 E19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr10:51586275 A>T maps to NM_001145260.1 V584V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr10:71684717 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr10:126523135 C>A maps to NM_032182.3 R282R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr11:66837994 C>A maps to NM_014578.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr11:118250227 C>T maps to NM_004788.2 Q554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr11:118373818 C>A maps to NM_001197104.1 T2404T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr11:119988940 G>A maps to NM_012101.3 F539F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr11:121448107 C>A maps to NM_003105.5 T1193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:2909051 A>G maps to NM_002014.3 Q236Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:7867785 T>A maps to NM_199286.2 S30S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:64609708 G>T maps to ENST00000311915 I90I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:67699343 G>A maps to NM_018448.3 L632L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:125453421 C>A maps to NM_032656.3 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr12:130185090 G>T maps to NM_133448.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr13:52992183 G>T maps to NM_016075.2 S283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr14:20845480 G>A maps to NM_007110.4 L2016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr14:68118140 C>T maps to NM_006370.2 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr14:100119114 C>G maps to NM_001127258.1 Y270*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr15:31819446 C>A maps to ENST00000382902 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr15:59064185 G>T maps to NM_001040450.1 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr15:75664532 G>A maps to NM_001145357.1 S1203S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr15:75672971 G>T maps to NM_001145357.1 P1127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr16:31146487 C>A maps to NM_002773.3 A30A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:7919109 G>A maps to NM_000180.3 L998L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:10223683 C>A maps to NM_003802.2 E1081*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:17174322 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:47696747 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:56164456 T>A maps to NM_080677.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:71192869 G>T maps to NM_018714.2 V180V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:73809277 C>A maps to NM_001080419.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr17:80382346 T>C maps to NM_173620.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr18:7955284 C>A maps to NM_001105244.1 S335S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr19:815809 C>A maps to NM_024888.1 L39L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr19:5592827 G>T maps to NM_014649.2 R760R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr19:14991894 G>A maps to NM_030901.1 V91V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr19:15198289 C>A maps to NM_001004713.1 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr19:46329550 G>T maps to NM_004819.2 L754L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr19:50504078 C>A maps to NM_016440.3 G194*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr19:55897757 G>T maps to NM_001136135.1 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr2:154334998 C>T maps to NM_019845.2 V27V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr2:219503115 C>A maps to NM_001105537.1 L1670L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr20:41100969 G>A maps to ENST00000373198 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr22:31724869 G>T maps to NM_014323.2 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr22:43213793 A>G maps to NM_014570.4 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr22:44235835 C>A maps to NM_014351.3 G124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr3:51978843 C>A maps to NM_001003931.2 S191S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr3:52282682 C>T maps to NM_144641.2 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr3:126137361 C>A maps to ENST00000505024 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr4:38037277 G>T maps to NM_015173.2 E458*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr4:57891053 A>G maps to NM_000938.1 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr4:72629624 C>A maps to ENST00000504199 G187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:2749874 G>T maps to NM_033267.4 T92T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:54591350 A>G maps to NM_019030.2 D169D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:76704767 G>T maps to NM_003719.3 A472A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:80508339 C>A maps to NM_006909.1 A1104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:139864823 T>C maps to ENST00000253810 H663H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:140021511 G>A maps to ENST00000252100 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:175958604 G>T maps to NM_014901.4 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:31627424 A>G maps to NM_021184.3 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:41303623 C>T maps to NM_004828.3 R4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:44140718 C>A maps to NM_007058.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr6:158450004 C>T maps to NM_003898.3 V144V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr7:21678589 C>A maps to NM_003777.3 Y1622*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr7:44607759 G>T maps to NM_019082.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr7:103008413 C>A maps to NM_002803.2 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr7:105656469 C>A maps to NM_152750.4 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:24251623 C>A maps to NM_014479.3 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:55534828 A>G maps to NM_006269.1 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:99152323 G>T maps to NM_015029.2 E461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr8:142238283 G>A maps to NM_001080431.1 Q28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr9:87570402 C>A maps to NM_006180.3 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr9:130207299 G>T maps to NM_007135.2 G441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr9:137645730 G>T maps to NM_000093.3 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chrX:47432307 G>C maps to NM_006950.3 T691T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chrX:65390504 C>T maps to NM_138737.3 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chrX:119603000 C>A maps to NM_013995.2 P8P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:16258647 T>C maps to NM_015001.2 P1971P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:24861604 G>T maps to NM_013441.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:25233806 G>T maps to NM_001031680.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:27875926 C>A maps to NM_001029882.2 V900V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:59125679 A>G maps to NM_001085487.1 L826L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:60228210 G>T maps to NM_001113411.1 L561L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:103449719 C>A maps to NM_080629.2 G856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:151379497 C>A maps to NM_015100.3 G812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:156933071 C>A maps to NM_198236.1 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:203739994 G>T maps to NM_017773.3 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:216246477 C>A maps to ENST00000366943 E1913*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:232561398 G>T maps to NM_020808.3 T1522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr1:249106475 C>A maps to NM_030645.1 E269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr10:6143262 C>A maps to NM_001145547.1 L51L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr10:12070796 G>T maps to NM_015542.2 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr10:73406334 C>T maps to ENST00000398860 Y475Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr10:81061946 C>A maps to NM_020338.3 P701P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr10:82049089 C>A maps to NM_000429.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr10:93695509 C>A maps to NM_003972.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:6501614 C>A maps to NM_012402.2 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:7720312 C>A maps to NM_198185.2 R303R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:46401422 G>T maps to NM_001105540.1 E1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:59420423 G>T maps to NM_152716.2 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:65338204 C>T maps to NM_006396.1 G50G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:66311411 C>A maps to NM_207340.1 G108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:66636375 G>T maps to NM_022172.2 Y321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:102573541 C>A maps to NM_022122.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr11:124793822 C>A maps to NM_152722.4 E171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr12:9010173 G>T maps to NM_144670.3 G1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr12:14613501 G>T maps to NM_018179.3 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr12:19626231 C>A maps to NM_001114176.1 T310T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr12:49943347 C>A maps to NM_012284.1 P531P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr12:50024388 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr12:54105786 C>A maps to NM_020898.2 E673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr12:109522869 C>A maps to NM_032663.3 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr12:113321141 C>A maps to NM_001143854.1 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr12:124184316 C>A maps to NM_024809.3 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr12:124333419 C>A maps to NM_207437.3 T1913T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr14:44974804 A>G maps to NM_032135.3 P462P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr14:74970089 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr14:75558160 C>A maps to NM_033116.4 G752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr15:35083347 G>T maps to NM_005159.4 I319I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr15:42127410 C>A maps to NM_005090.3 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr15:55965710 C>A maps to NM_173814.4 P570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr15:62170918 G>T maps to NM_020821.2 S3343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr15:65234725 C>A maps to NM_182703.3 L310L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr15:91500667 G>A maps to NM_033544.2 E164E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr16:3077634 C>A maps to NM_024339.3 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr16:12096891 C>A maps to NM_032167.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr16:29810321 G>T maps to NM_007317.1 S192S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr16:67237686 G>T maps to NM_024712.3 L743L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr16:70509620 G>T maps to NM_145059.2 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr16:70710802 G>T maps to NM_138383.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr16:74694858 G>T maps to NM_018124.3 A163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:7224215 G>T maps to NM_032442.2 P1129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:7366575 C>A maps to NM_020899.3 V575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:7674685 C>A maps to NM_020877.2 P1467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:18003956 C>A maps to NM_001388.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:44828975 C>A maps to NM_006178.2 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:48277246 G>T maps to NM_000088.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:58234896 G>T maps to NM_000717.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:73746315 G>A maps to NM_001005619.1 W1147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:78169386 G>T maps to NM_024110.2 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr17:78320174 C>A maps to NM_020914.4 P2729P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:7976337 A>G maps to ENST00000425613 G360G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:8578168 G>T maps to NM_001146175.1 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:10528352 C>A maps to ENST00000380702 P22P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:12502923 A>T maps to NM_001080821.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:17132954 C>A maps to ENST00000443236 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:19656521 C>A maps to NM_153221.2 G1056G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:38572673 C>A maps to NM_015073.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:41782092 C>A maps to NM_007040.3 R226R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:42729448 G>T maps to NM_133444.1 P298P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr19:49705257 C>A maps to NM_017636.3 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:17919548 C>A maps to ENST00000381272 G121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:21260121 G>T maps to NM_000384.2 T181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:46234703 C>A maps to NM_005400.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:46603857 C>A maps to NM_001430.4 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:64863063 G>T maps to NM_014755.2 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:96781258 C>T maps to NM_000682.5 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr2:179611916 T>C maps to ENST00000375038 L5072L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr20:400299 C>A maps to NM_031229.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr20:15918145 C>A maps to ENST00000310348 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr20:41101086 G>T maps to ENST00000373198 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr20:43739408 C>A maps to ENST00000307971 S31S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr21:45507796 C>A maps to NM_003274.4 T919T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr21:45877226 C>A maps to NM_030891.3 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr22:18029011 G>T maps to ENST00000400579 T1324T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr22:50547181 C>A maps to NM_018995.2 R218R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr22:50728010 G>T maps to NM_012401.2 R335R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:23942483 G>A maps to NM_020345.3 R51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:49316260 C>A maps to NM_003363.3 E907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:50365407 G>T maps to NM_007275.1 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:51457621 C>G maps to ENST00000273612 R934R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:123038665 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:164700036 G>T maps to NM_001041.3 T1803T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:185146746 C>T maps to NM_004721.3 G126G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:194174465 G>T maps to NM_024524.3 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr4:949634 G>T maps to NM_032326.2 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr4:6303093 C>T maps to NM_006005.3 F524F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr4:39322973 C>A maps to ENST00000381897 A247A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr4:57314735 C>A maps to NM_001079525.1 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr5:163210 A>G maps to NM_052909.3 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr5:32088029 C>A maps to NM_178140.2 P1492P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr5:33561146 C>A maps to NM_030955.2 V1370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr5:82406898 G>T maps to NM_022406.2 G64G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr6:18207699 C>A maps to ENST00000388870 P577P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr6:31138184 C>A maps to NM_002701.4 G71G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr6:46135579 G>T maps to NM_021572.4 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr6:64395770 C>A maps to NM_015153.2 P716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr6:110086259 C>A maps to NM_014845.5 T493T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr6:157256649 C>A maps to ENST00000367148 P646P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr6:158483049 G>T maps to NM_003898.3 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr7:5633076 C>A maps to ENST00000340250 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr8:3063041 C>A maps to NM_033225.5 T1656T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr8:41522409 C>A maps to NM_020478.4 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr8:48612970 G>T maps to NM_001080394.1 A564A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr8:109215295 A>T maps to NM_001568.2 I405I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr8:142228715 G>T maps to NM_001080431.1 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr8:143996169 G>T maps to NM_000498.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:990227 C>A maps to NM_021240.2 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:34385743 G>T maps to NM_032596.3 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:39140599 G>A maps to NM_033655.3 R598*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:85928662 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:90301616 C>A maps to NM_004938.2 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:96079878 C>A maps to ENST00000297954 P2235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:98218572 G>T maps to NM_000264.3 T1097T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:99580815 G>T maps to NM_001001662.1 R497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:101552758 G>T maps to ENST00000375018 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:116353654 C>A maps to NM_144488.4 R1020R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:131277806 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:131783492 G>T maps to ENST00000372554 R71R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:132641858 C>A maps to NM_001008563.3 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr9:138908135 G>T maps to NM_144653.3 P342P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chrX:2871265 G>T maps to NM_000047.2 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chrX:49113449 C>A maps to ENST00000455775 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chrX:101096013 T>A maps to ENST00000263032 K152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chrX:105144628 G>T maps to NM_198465.2 G244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chrX:153593595 C>A maps to NM_001110556.1 L533L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr11:64522810 G>A maps to NM_005609.2 Y263Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr11:67289449 G>T maps to NM_016366.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr19:35232371 A>G maps to ENST00000392232 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr3:124632010 A>G maps to NM_033049.3 P386P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr6:49931769 G>A maps to NM_001037499.1 L17L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr8:126448647 G>T maps to NM_025195.2 G352*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chr9:13183482 A>G maps to ENST00000319217 S861S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chrX:128895979 A>G did not map to a codon.
Sequencing variant TCGA-BQ-7055-01A-11D-1961-08 chrX:151870044 G>A maps to NM_005363.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:19500066 C>A maps to ENST00000375267 G1011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:32119277 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:37948497 C>A maps to NM_025079.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:40435180 G>T maps to NM_001136493.1 E525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:43777753 G>T maps to NM_005424.2 G528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:44064421 G>T maps to NM_002840.3 V717V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:45250977 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:53287195 T>C maps to NM_024646.2 H710H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:76378535 C>A maps to NM_002440.2 P925P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:118496662 C>A maps to NM_006784.2 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:150931732 C>A maps to NM_001145415.1 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:151342001 G>T maps to ENST00000435071 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:200944755 G>T maps to NM_017596.2 P1482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:201186587 G>T maps to NM_001164586.1 E3257*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:202107543 G>T maps to NM_138795.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:209804044 G>T maps to NM_000228.2 A286A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:233511776 C>A maps to NM_032435.2 S597S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr1:247751933 C>A maps to NM_001001915.1 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr10:69750915 C>A maps to NM_022079.2 G438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr10:90975766 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr10:90983533 C>A maps to NM_000235.2 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr10:134012449 C>T maps to NM_006426.2 D262D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr11:3128609 G>T maps to NM_020896.3 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr11:6622548 G>T maps to NM_015324.2 A249A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr11:34186368 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr11:46401095 C>A maps to NM_001105540.1 S1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr11:57268293 C>A maps to NM_003627.5 L141L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr11:62455659 G>T maps to NM_203422.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr11:63670253 G>T maps to NM_001039469.2 T472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr11:65685349 C>A maps to NM_001135635.1 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr11:77412530 G>T maps to NM_016578.3 I581I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr11:111753249 C>T maps to NM_022761.2 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr12:6946953 G>A maps to NM_014262.3 L589L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr12:12483323 C>A maps to NM_018050.2 T311T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr12:52184276 C>A maps to NM_014191.2 P1505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr12:56489542 C>A maps to NM_001982.2 R670R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr12:62798044 C>A maps to ENST00000280377 R946R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr12:113906072 G>T maps to NM_022363.2 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr13:47263285 G>T maps to NM_001164211.1 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr13:67800361 C>A maps to NM_203487.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr13:113814379 G>T maps to ENST00000342783 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr14:97299933 C>A maps to NM_003384.2 P42P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr15:28431769 T>C maps to NM_004667.4 L2926L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr15:28519477 C>A maps to NM_004667.4 V253V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr15:40594675 C>A maps to NM_004573.2 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr15:40633026 G>T maps to NM_207380.2 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr15:42035308 G>T maps to ENST00000219905 L1766L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr15:89449123 C>A maps to NM_005928.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr15:99740159 C>A maps to NM_022905.4 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr16:135622 C>A maps to NM_002434.2 P248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr16:2049728 G>T maps to ENST00000431526 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr16:23391986 C>A maps to ENST00000307331 P641P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr16:28502878 C>A maps to NM_000086.2 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr16:31422759 G>T maps to ENST00000444228 P559P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr16:71768553 C>A maps to ENST00000423132 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr17:7106600 C>A maps to NM_001365.3 G228*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr17:7804298 C>A maps to NM_001005271.2 P1095P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr17:11520830 G>C maps to NM_001372.3 R336R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr17:76170983 G>T maps to NM_003258.4 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr18:3582120 C>A maps to NM_004746.2 G573*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr19:3006495 C>A maps to NM_003260.4 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr19:5610038 C>A maps to NM_014649.2 T421T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr19:7914167 G>T maps to NM_001159944.1 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr19:18966850 C>A maps to ENST00000418384 S565S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr19:36214828 C>A maps to NM_014727.1 S1085S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr19:48343160 C>A maps to NM_000554.4 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:11944574 C>A maps to ENST00000396099 P686P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:44428533 C>A maps to NM_002706.4 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:70444050 G>T maps to NM_022173.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:71747337 C>A maps to NM_001130987.1 R345R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:88857310 C>A maps to NM_004836.5 S1098S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:141259267 C>A maps to NM_018557.2 P2946P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:172950597 C>A maps to NM_178120.4 R65R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:182322940 C>A maps to NM_000885.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:203839086 C>A maps to NM_024744.14 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:207041107 G>T maps to NM_005279.3 L288L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:224760260 C>A maps to NM_020830.3 G229*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:233345474 G>T maps to NM_004826.2 R702R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr2:242607956 G>T maps to ENST00000337606 E388*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr20:3765360 C>A maps to NM_001810.5 A590A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr20:13273070 G>T maps to NM_080826.1 G280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr20:30671800 C>A maps to NM_002110.3 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr20:56929244 C>A maps to NM_020673.2 A137A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr20:61941125 G>T maps to ENST00000326996 L381L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr21:33976443 C>A maps to NM_021254.2 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr21:45548465 C>A maps to NM_005049.2 L848L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr22:26830060 C>A maps to NM_020437.4 P160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr22:39411695 C>A maps to ENST00000396762 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr3:48447206 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr3:48602252 G>A maps to NM_000094.3 R2927R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr3:57542201 G>T maps to NM_177966.5 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr3:183994312 C>A maps to NM_001100120.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr3:195968961 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr4:728768 C>A maps to NM_006315.4 P53P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr4:16597382 C>A maps to NM_001290.3 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr4:26719572 C>A maps to NM_018317.2 R325R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr4:47877310 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr4:144460069 C>A maps to NM_003601.2 P583P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr5:50683395 C>A maps to NM_002202.2 S97S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr5:74695137 G>T maps to NM_001130105.1 S523S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr5:131307301 C>A maps to NM_001009185.1 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr6:31855950 C>A maps to ENST00000395728 E595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr6:33236281 C>A maps to NM_022553.4 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr6:99924029 C>A maps to NM_001080481.1 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr6:144269138 G>T maps to NM_001080951.1 S45S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr6:146007354 C>A maps to NM_005670.3 G127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr6:152730719 C>A maps to NM_182961.2 E2119*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr7:6623051 C>A maps to NM_018106.3 S162S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr7:75401235 G>C maps to NM_006072.4 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr7:150070003 C>A maps to NM_001099695.1 L615L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr8:17541992 G>T maps to NM_001001924.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr8:95502250 G>T maps to NM_015496.3 R1734R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr8:100874007 C>A maps to NM_017890.3 T3708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr8:104066207 C>A maps to NM_001695.4 P190P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr9:7013852 G>T maps to NM_015061.3 S678S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr9:118950480 C>A maps to NM_002581.3 P488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr9:128067395 C>A maps to NM_015635.2 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr9:130687539 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr9:136305531 C>A maps to NM_139025.3 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr9:139391476 G>T maps to NM_017617.3 P2238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chrX:34961004 C>A maps to NM_152631.2 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chrX:129148238 C>A maps to ENST00000303743 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chrX:152085711 C>A maps to NM_001178106.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:52798489 C>A maps to NM_004799.2 A1163A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:67423740 G>C did not map to a codon.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:110774882 T>C maps to NM_004978.4 P620P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:147086308 A>C maps to NM_004326.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:236195869 A>G maps to NM_002508.2 T456T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr1:237829828 C>A maps to NM_001035.2 A2818A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr10:73491996 G>T maps to ENST00000398860 L1328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr11:281107 G>C maps to NM_138329.1 A458A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:26490599 A>G maps to NM_016231.4 L261L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:62500169 T>C maps to NM_004396.3 G124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr17:72745285 A>T maps to NM_004252.3 K101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr18:21819190 C>A maps to NM_080597.2 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr19:3433549 C>A maps to ENST00000269778 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr19:43237191 G>T maps to NM_021016.3 I151I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr2:37280724 C>A maps to NM_019024.1 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr2:109379712 T>C maps to NM_006267.4 N906N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr2:136505918 T>C maps to NM_014607.3 A55A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr3:52584608 A>T maps to ENST00000296302 Y1575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr4:88029421 A>T maps to NM_001166693.1 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr5:916036 C>T maps to NM_004237.3 S384S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr5:134910375 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr5:176637985 C>T maps to NM_022455.4 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr6:7889003 A>C maps to NM_030810.3 T299T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BQ-7058-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chr8:35541183 C>T maps to ENST00000416672 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:4832567 C>A maps to NM_018836.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:7721864 C>A maps to NM_015215.2 L248L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:10166407 G>T maps to NM_001105562.2 A321A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:15793928 C>T maps to ENST00000375924 Q267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:16378295 A>C maps to NM_000085.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:26515114 C>A maps to ENST00000374253 P546P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:33246689 G>T maps to NM_003680.3 R367R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:36551576 G>T maps to NM_014466.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:72058647 G>T maps to NM_173808.2 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:84417639 G>T maps to NM_024686.4 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:151786054 G>T maps to ENST00000392697 T379T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:153723579 C>A maps to ENST00000428986 V199V. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BQ-7059-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:156933096 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:178412264 C>A maps to ENST00000263528 T443T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:184476744 G>T maps to NM_030806.3 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:204091058 C>A maps to ENST00000367206 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:223984098 A>G maps to NM_001031685.2 N714N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:231114977 G>T maps to NM_022786.1 E43*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr1:240635687 G>T maps to ENST00000406993 E1836*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr10:98386588 C>A maps to NM_152309.2 T515T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr10:99338145 C>A maps to NM_020349.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr10:103559015 G>T maps to NM_012215.3 P464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr10:105785453 C>A maps to NM_014720.2 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:1029134 C>A maps to NM_005961.2 E431*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:48238453 C>A maps to NM_001005470.1 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:55606580 G>T maps to NM_001005496.1 A118A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:61615704 C>A maps to NM_004265.2 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:62494157 G>T maps to NM_001079559.1 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:66291247 C>A maps to NM_024649.4 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:82705164 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:118849784 C>A maps to NM_181721.2 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:120745882 C>T maps to NM_014619.2 F365F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr11:134183842 G>T maps to NM_001080407.2 G530*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:1904888 G>T maps to NM_172364.4 P1057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:2716230 C>T maps to NM_199460.2 D1117D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:4383268 C>A maps to NM_001759.3 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:8975819 C>A maps to NM_144670.3 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:26639153 C>A maps to NM_002223.2 A1898A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:50500138 C>A maps to NM_005276.2 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:52946834 C>A maps to NM_033448.2 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:53937185 C>A maps to NM_001130059.1 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:56749080 G>T maps to NM_005419.3 R176R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:57965858 C>A maps to NM_004984.2 R460R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:85695060 G>T maps to NM_006982.2 T263T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:95663825 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:110933885 G>T maps to NM_057180.1 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr12:113327858 C>A maps to NM_001143854.1 R532R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr13:39448721 C>A maps to NM_207361.4 P2760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr13:114762014 G>T maps to ENST00000389544 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr14:21792933 C>A maps to NM_020366.3 A640A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr14:21992673 C>A maps to NM_005407.1 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr14:23876445 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr14:68087636 C>A maps to NM_001172.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr14:77706023 C>A maps to NM_020431.2 P295P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr14:81744520 G>A maps to NM_033104.2 H378H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr14:105239222 G>T maps to NM_001014432.1 P388P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr14:105405034 C>A maps to NM_138420.2 G5585*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr15:41814439 G>T maps to NM_015540.2 A917A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr15:43352291 C>A maps to NM_174916.2 A273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr15:53889438 C>A maps to NM_182758.2 A995A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr15:64915130 C>A maps to NM_015042.1 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr15:77087750 A>T maps to ENST00000324767 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr15:90897951 C>A maps to NM_001004309.2 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:684560 G>T maps to NM_001040160.1 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:2550898 C>A maps to ENST00000434757 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:4524102 C>A maps to NM_020677.3 G11*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:15126762 C>A maps to NM_015027.2 P539P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:28498807 G>T maps to NM_000086.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:67233264 C>A maps to NM_024712.3 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:70590233 C>A maps to NM_012426.4 P621P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:70884520 C>A maps to NM_032821.2 G4160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:71483579 G>T maps to NM_145911.1 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:72138440 G>T maps to NM_014003.3 A689A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr16:87902689 C>A maps to NM_003486.5 S113S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:2276783 C>A maps to NM_014853.2 R693R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:4643995 C>A maps to NM_001136046.1 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:6012934 C>G maps to NM_015253.1 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:7345152 G>T maps to NM_004112.2 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:33289280 T>C maps to NM_052857.3 H232H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:38253600 A>G maps to NM_021724.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:38546393 G>T maps to ENST00000357601 T1467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:40263500 G>T maps to NM_024119.2 T61T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:40839049 C>A maps to NM_003632.2 R344R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:42030535 C>A maps to NM_004160.4 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:42927752 G>T maps to NM_016438.2 G97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:48667833 C>A maps to NM_018896.3 P768P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:65052342 C>A maps to NM_000727.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:67077255 G>T maps to NM_080284.2 P1549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:72860156 C>A maps to ENST00000442102 T388T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:73501067 C>A maps to NM_020753.3 P339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:73922916 C>A maps to ENST00000389570 G159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:76113394 C>A maps to NM_007267.6 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr17:80274699 C>A maps to NM_006137.6 T80T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr18:31251777 C>A maps to NM_030632.1 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:1924168 G>A maps to NM_079834.2 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:4231296 C>A maps to NM_005755.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:4323573 C>A maps to NM_024333.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:4792438 C>A maps to NM_018708.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:5110772 C>A maps to NM_015015.2 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:6418003 G>T maps to NM_003685.2 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:7619509 G>A maps to NM_001166111.1 Q855Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:7831073 C>A maps to NM_014257.4 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:10439479 C>A maps to NM_133452.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:12876929 C>A maps to NM_013312.2 E500*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:13201165 C>A maps to ENST00000397661 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:15904881 C>A maps to NM_001004466.1 S8S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:17780373 C>A maps to ENST00000428389 E216*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:38866810 G>T maps to NM_002812.4 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:39322403 C>A maps to NM_001398.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:39412273 G>T maps to NM_017827.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:40711979 C>A maps to NM_002446.3 R451R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:47575640 G>T maps to NM_015168.1 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:48954338 C>A maps to NM_031485.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:50397530 G>C maps to NM_172374.1 L209L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:50936216 G>T maps to NM_004533.3 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:51273913 G>C maps to NM_001506.1 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr19:58084257 A>G maps to NM_017879.1 S338S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:15536550 C>A maps to NM_015909.2 L1040L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:25039672 C>A maps to NM_024322.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:27564843 G>T maps to NM_001521.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:38545712 C>A maps to NM_001135673.1 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:48026288 C>A maps to NM_000179.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:55844409 C>T maps to NM_001122964.1 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:68358408 C>A maps to NM_138458.2 T345T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:74598810 G>T maps to NM_004082.4 S166S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:85255010 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:85549812 A>T did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:116572491 T>C maps to NM_020868.3 G608G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:155566146 C>A maps to NM_002239.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:207988747 C>A maps to NM_003709.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:209209894 C>A maps to NM_015040.3 A1696A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:219696489 C>A maps to NM_017431.2 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr2:238733058 G>T maps to NM_001080504.2 G817*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr20:77012 C>A maps to NM_153325.2 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr20:3302863 C>A maps to NM_001009984.1 T452T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr20:8639211 C>A maps to NM_015192.2 T241T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr20:33329157 C>A maps to NM_014071.2 A1634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr20:47691343 A>G maps to NM_001316.2 E363E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr20:61588305 C>A maps to NM_022082.3 L83L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr20:62851172 C>A maps to NM_004535.2 P693P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr22:29913072 C>A maps to NM_003678.4 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr22:30738225 C>A maps to NM_005877.4 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr22:32804229 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:38760179 G>T maps to NM_006514.2 T1215T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:49947904 G>T maps to NM_032355.3 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:51352436 G>T maps to NM_004947.4 G1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:64601665 C>A maps to NM_182920.1 T998T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:81584370 G>T maps to ENST00000264326 R637R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:87017992 C>T maps to NM_016206.2 R228R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:122414351 G>A maps to NM_017554.2 V226V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:124461052 C>A maps to NM_000373.3 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:126208212 C>A maps to NM_001165974.1 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr3:130405106 C>A maps to NM_014602.2 S1141S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr4:6599998 G>T maps to NM_015274.1 S441S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr4:37848677 C>A maps to NM_018290.3 T378T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr4:79832187 C>A maps to NM_198892.1 T829T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr4:107157965 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr4:185039053 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr4:187196991 G>T maps to NM_000128.3 T179T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:9224845 G>T maps to NM_003966.2 R196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:11384870 G>T maps to NM_001332.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:80422899 G>T maps to NM_006909.1 T868T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:95067766 G>T maps to NM_014899.3 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:126753365 G>T maps to NM_032446.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:128983498 T>C maps to NM_133638.3 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:131976366 T>C maps to NM_005732.3 L1208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:140773678 C>A maps to NM_032088.1 S433S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr5:140802437 G>C maps to NM_018914.2 S548S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:25967010 G>C maps to NM_006355.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:29408019 G>T maps to NM_013941.2 T76T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:31515488 C>A maps to NM_005007.3 P6P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:32370751 G>T maps to ENST00000468270 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:42957392 G>T maps to NM_006245.2 S24S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:74079013 G>T maps to NM_001080507.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:119222018 C>A maps to NM_014034.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:152466676 G>T maps to NM_033071.2 P8259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr6:154732271 C>A maps to NM_173515.2 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:4153004 C>A maps to NM_152744.3 P1173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:6456270 G>T maps to NM_139179.3 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:23299722 C>A maps to ENST00000435486 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:75174098 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:87145824 C>A maps to NM_000927.3 P1028P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:99802727 C>A maps to NM_012447.2 R1018R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:138602844 G>T maps to NM_001164665.1 A509A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:142606737 C>A maps to NM_019841.4 E605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:149129808 G>T maps to ENST00000440594 P519P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:149463182 C>A maps to NM_207336.1 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:149500083 C>A maps to NM_198455.2 S2571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr7:150558050 G>T maps to ENST00000416793 T689T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr8:21955262 C>A maps to NM_022749.5 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr8:39044453 A>G maps to NM_145004.5 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr8:95789953 C>A maps to NM_181787.2 P505P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr8:106813920 C>A maps to NM_012082.3 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr8:126114557 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr8:144332426 G>T maps to NM_173832.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr9:32553942 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr9:72755149 C>A maps to NM_153267.4 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr9:113547908 C>A maps to ENST00000189978 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr9:116136534 G>T maps to NM_031219.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr9:123210191 G>T maps to NM_018249.4 P1002P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chr9:132576387 G>T maps to ENST00000437532 R320R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:9864090 G>T maps to NM_001649.2 E715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:11682426 G>T maps to NM_013427.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:18622106 C>A maps to NM_001037343.1 R355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:46359546 C>A maps to NM_001039891.2 G493*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:49142726 C>A maps to NM_033215.4 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:53607920 G>T maps to ENST00000276009 L1862L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:54264843 G>T maps to NM_020922.4 S1315S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:70349662 G>T maps to ENST00000333646 L1275L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:107826112 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:117528054 C>A maps to NM_019045.4 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:122770006 A>G maps to NM_001081550.1 G647G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:129055381 C>A maps to NM_006649.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7059-01A-11D-1961-08 chrX:129201031 C>A maps to NM_001127197.1 T552T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:1887180 G>T maps to ENST00000434971 R709R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:9655946 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:17280746 G>T maps to NM_014675.3 T1072T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:19212100 C>A maps to NM_003748.3 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:21220041 C>A maps to NM_001198801.1 G684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:22903098 G>T maps to NM_020526.3 L183L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:27614199 G>T maps to ENST00000319394 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:27683138 C>A maps to NM_004672.3 E1156*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:31230523 G>T maps to NM_006762.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:33272091 G>T maps to NM_003680.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:38079411 G>T maps to NM_001038633.2 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:39782939 G>T maps to ENST00000361689 E1220*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:39919464 C>A maps to ENST00000361689 P4884P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:39919497 C>A maps to ENST00000361689 T4895T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:45292171 C>A maps to NM_003738.4 T988T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:52276003 C>A maps to NM_002525.2 G686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:145581540 C>A maps to NM_006099.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:149916178 C>A maps to NM_020205.2 G703G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:150971952 C>A maps to NM_001163258.1 A339A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:153926750 G>T maps to NM_181715.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:153946369 C>A maps to NM_130898.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:154940250 G>T maps to NM_001130040.1 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:155039289 C>A maps to NM_182689.1 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:155911940 G>T maps to NM_181885.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:156882319 C>A maps to NM_001080471.1 S705S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:158063506 C>A maps to ENST00000368173 T574T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:158597434 C>A maps to NM_003126.2 G1882*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:161011552 G>T maps to NM_007122.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:180885892 C>A maps to NM_020950.1 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:183093811 G>T maps to NM_002293.3 L816L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:207639946 C>A maps to NM_001006658.2 T45T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr1:224619226 C>A maps to NM_025160.6 V193V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr10:70987114 C>A maps to NM_025130.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr10:75526263 G>T maps to NM_198597.1 L588L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr10:88485939 C>A maps to NM_001171610.1 P680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr10:95418899 C>A maps to NM_006204.3 T728T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr10:97127432 C>A maps to NM_001034954.1 P643P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr10:97392769 G>T maps to NM_002860.3 R252R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr10:115963151 G>T maps to NM_198795.1 T269T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr10:122643354 C>A maps to NM_018117.11 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr10:123846913 C>A maps to NM_206862.2 A1633A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr10:123988919 C>A maps to NM_206862.2 P2652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:4790879 C>A maps to ENST00000380383 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:7439308 C>A maps to NM_175733.3 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:10014059 C>A maps to NM_030962.3 E400*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:10800231 C>A maps to NM_014633.3 P1034P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:18738392 C>A maps to NM_173588.3 T376T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:31824373 C>A maps to NM_001604.4 G7*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:44253940 G>T maps to NM_000401.3 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:55418987 C>A maps to NM_001004059.2 T203T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:59245150 G>T maps to NM_001004705.1 V83V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:60636708 C>A maps to NM_207341.2 A96A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:61503046 C>A maps to NM_006133.2 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:63885448 G>T maps to NM_013280.4 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:64074869 C>A maps to NM_004451.3 S73S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:64603242 G>T maps to NM_017525.2 S583S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:71701756 C>A maps to NM_018320.4 T207T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:71717297 C>A maps to ENST00000393695 V1831V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:76171052 G>T maps to ENST00000393457 T166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:94278513 C>A maps to NM_002033.3 A405A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:94592856 C>A maps to NM_130847.2 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:113270775 C>A maps to NM_178510.1 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:113614713 C>A maps to NM_004724.2 E441*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:116728955 C>A maps to ENST00000445177 A1068A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:117395655 C>A maps to NM_020693.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:119144722 C>A maps to NM_005188.2 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr11:130011926 G>T maps to NM_001642.2 L716L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:1675975 C>A maps to NM_152441.2 E399*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:1863530 C>A maps to NM_024551.2 R8R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:12629993 C>A maps to NM_030640.2 G591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:31632577 C>A maps to NM_144973.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:48192411 G>T maps to NM_015401.3 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:56346169 C>A maps to NM_201554.1 S566S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:57501526 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:57600439 C>A maps to NM_002332.2 S3925S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:58021605 G>T maps to NM_001478.3 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:71965292 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:78513452 C>A maps to NM_014903.4 T1159T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:104081962 C>A maps to NM_017564.9 S1005S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:121593946 C>A maps to NM_002562.5 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr12:121598737 C>A maps to NM_002562.5 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr13:50038155 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr13:98828599 G>T maps to NM_178861.4 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr13:99118674 G>T maps to NM_003576.3 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr13:107211877 G>T maps to NM_018011.3 R159R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr13:113478730 C>A maps to NM_032189.3 A288A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr14:20922833 C>A maps to NM_017807.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr14:23899872 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr14:24567799 C>A maps to NM_004563.2 R193R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr14:31774323 C>A maps to ENST00000389961 G1670*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr14:39555061 C>A maps to NM_006364.2 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr14:64882194 C>A maps to NM_005956.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr14:68047704 C>A maps to NM_020715.2 P1078P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr14:74766250 C>A maps to NM_005050.3 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr14:105185141 C>A maps to NM_001031714.3 P1235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr15:41770783 C>A maps to NM_015138.4 P593P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr15:45396440 G>T maps to NM_014080.4 P819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr15:50264983 C>A maps to NM_024837.2 V346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr15:54542517 C>A maps to ENST00000260323 P1108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr15:55497727 C>A maps to NM_183235.1 E215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr15:57731089 C>A maps to NM_032866.3 S298*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr15:64019984 G>T maps to ENST00000261887 S1069S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr15:75685138 C>A maps to NM_001145357.1 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr15:79058001 C>A maps to ENST00000258883 A1417A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr15:80762615 G>T maps to NM_014862.3 T84T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr15:86123377 C>A maps to NM_006738.4 T693T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:1265547 G>T maps to NM_021098.2 T1733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:1509125 G>T maps to ENST00000382745 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:1825334 C>A maps to NM_001010865.1 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:2980826 C>A maps to ENST00000399667 R248R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:8870206 C>A maps to NM_001127448.1 R377R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:18805972 C>A maps to NM_015161.1 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:22159558 C>A maps to NM_173615.3 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:22274499 C>T maps to NM_013302.3 R457*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:24942602 G>T maps to NM_001006634.1 R673R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:30749631 G>T maps to NM_006662.2 V2757V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:31383748 G>A maps to NM_000887.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:67168084 T>C maps to NM_025187.3 H155H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:67577131 G>T maps to NM_001193523.1 E835*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:67979969 G>T maps to NM_005072.4 R875R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:83940665 C>A maps to NM_012213.2 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:84476138 G>T maps to ENST00000416219 A445A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr16:88723975 G>T maps to NM_002461.1 R91R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:10267724 C>T maps to NM_003802.2 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:18075033 C>A maps to ENST00000205890 R3389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:41243809 G>T maps to ENST00000471181 T1246T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:41909258 C>A maps to ENST00000398393 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:43220855 C>A maps to NM_001135706.1 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:47121336 C>A maps to NM_006546.3 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:56643156 G>T maps to ENST00000240361 S1351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:72363721 G>T maps to NM_181790.1 L26L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:72920906 C>A maps to NM_178160.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:72999979 G>T maps to NM_014603.2 G403G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:74084586 G>T maps to NM_001145297.2 T470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr17:78341808 C>A maps to NM_020914.4 P4056P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr18:7007164 G>T maps to NM_005559.2 T1411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr18:7007191 G>T maps to NM_005559.2 P1402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr18:29704750 C>A maps to NM_001191324.1 T205T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr18:47091702 C>A maps to NM_006033.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr18:72775791 G>T maps to NM_017757.2 E2039*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr18:77960799 G>T maps to NM_032510.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:498520 C>A maps to NM_130760.2 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:5696707 C>A maps to NM_004793.2 T582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:7081458 C>A maps to NM_024341.2 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:7621349 G>T maps to NM_001166111.1 S1045S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:10116871 C>A maps to NM_015719.3 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:10218643 C>A maps to NM_001040664.2 S116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:10405234 C>A maps to NM_003259.3 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:11304698 G>T maps to NM_015493.6 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:11363550 G>T maps to ENST00000319867 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:12432146 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:14003598 C>A maps to ENST00000454313 L131L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:17845144 C>A maps to NM_018174.4 R1030R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:18499252 C>A maps to NM_004864.2 L145L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:18779556 C>A maps to NM_018316.1 T450T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:19613157 C>A maps to ENST00000404158 R552R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:20728762 G>T maps to NM_001159293.1 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:31767881 G>T maps to NM_020856.2 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:36038327 C>A maps to NM_032635.2 A218A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:36545086 G>T maps to NM_152658.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:38905637 G>T maps to ENST00000405332 S361S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:42492117 C>A maps to ENST00000441343 A109A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:43969647 C>A maps to NM_014400.2 G26*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:45528637 C>A maps to ENST00000221452 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:49309887 G>T maps to NM_001190.3 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:49351222 C>A maps to NM_020904.2 P500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:50387771 G>T maps to NM_024682.2 E434*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr19:58724136 C>A maps to NM_133502.1 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:41612 G>T maps to NM_001077710.2 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:10822139 G>T maps to NM_024894.2 T56T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:11955273 G>T maps to ENST00000396099 R776R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:29165212 C>A maps to NM_015131.1 S590S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:32667467 G>T maps to NM_016252.3 E1395*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:37259898 G>T maps to NM_019024.1 S1078S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:43819123 C>A maps to ENST00000330266 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:46378223 C>A maps to NM_005400.2 A592A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:54587345 G>T maps to NM_001100396.1 G171*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:55602019 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:70122251 C>A maps to NM_006857.1 R21R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:71060051 C>A maps to NM_015717.3 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:71206870 C>A maps to NM_001115116.1 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:87013078 C>A maps to ENST00000456996 S265S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:110053583 C>A maps to NM_001099289.1 R604R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:120635091 C>A maps to NM_002830.2 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:128408629 C>A maps to NM_005291.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:128917200 C>A maps to NM_020120.3 S823S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:153476164 C>A maps to NM_052905.3 P590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:162036221 C>A maps to NM_004180.2 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:165768154 C>A maps to ENST00000409662 V262V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:169847417 C>A maps to NM_003742.2 T267T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:179648810 C>A maps to NM_133378.4 G921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:198274608 C>A maps to NM_012433.2 A263A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:217525368 C>A maps to NM_000597.2 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:219503453 G>T maps to NM_001105537.1 R1558R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:220418408 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:239039022 C>A maps to NM_194312.2 P556P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr2:242097274 G>T maps to NM_002712.1 E79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr20:170227 C>A maps to NM_001037732.1 E13*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr20:472935 G>T maps to NM_177559.2 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr20:14308035 C>A maps to NM_198391.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr20:18139769 C>A maps to NM_020536.4 L181L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr20:30450487 C>A maps to NM_080611.3 T107T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-BQ-7060-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr20:34022108 G>T maps to ENST00000374375 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr20:43378788 G>T maps to ENST00000372861 P101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr20:43959147 G>T maps to NM_002999.2 T101T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr20:46264254 G>T maps to NM_181659.2 G434G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr21:27372471 C>A maps to NM_000484.3 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr21:37445137 C>A maps to NM_001757.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr21:40188983 C>A maps to NM_005239.4 S186S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr21:44836654 G>T maps to NM_173354.3 P773P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr22:24573649 C>A maps to NM_012295.3 P2128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr22:26895231 G>T maps to NM_012143.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr22:35729473 C>A maps to ENST00000451197 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr22:36689445 G>T maps to NM_002473.4 R1342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr22:38121211 C>A maps to NM_001039141.2 P883P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr22:39884584 C>A maps to NM_001098270.1 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr22:40708611 C>A maps to ENST00000454349 P1527P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr22:41916278 G>T maps to ENST00000396512 V404V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr22:43572392 C>A maps to NM_015140.3 E284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr22:50588097 G>T maps to NM_018995.2 P894P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr22:51016338 C>A maps to NM_152245.2 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:47044742 C>A maps to NM_015175.1 P1888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:51112852 C>A maps to NM_004947.4 V177V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:52029444 G>A maps to NM_000992.2 N11N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:52409371 G>T maps to ENST00000273600 E2368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:52538089 G>T maps to NM_015136.2 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:53381424 G>T maps to ENST00000480258 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:62188893 G>T maps to NM_002841.3 S475S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:100100547 C>A maps to NM_014820.3 T265T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:113092403 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:122044171 C>A maps to NM_005213.3 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:122146563 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:124160889 C>A maps to NM_001024660.3 P1097P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:126152008 C>A maps to ENST00000505024 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:127294884 C>A maps to NM_001136053.1 L169L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:133666244 C>A maps to NM_005630.2 G384*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:160249254 A>G maps to NM_002268.3 D126D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:178968831 C>A maps to NM_014407.3 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:189838049 G>T maps to NM_018192.3 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr3:195595542 G>T maps to NM_001010938.1 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:2824665 C>A maps to NM_001145856.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:6114541 G>T maps to NM_001099433.1 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:9982230 G>T maps to NM_020041.2 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:17528677 G>T maps to NM_001079827.2 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:69798432 C>A maps to NM_024743.3 V303V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:70148238 C>A maps to NM_053039.1 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:86916654 G>T maps to NM_001025616.2 V616V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:88036381 C>A maps to NM_001166693.1 P799P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:89660227 G>T maps to NM_014883.2 R839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:111026784 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:123814147 G>T maps to NM_007083.3 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:129100598 C>A maps to NM_018078.2 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:155237038 G>T maps to NM_017639.3 S1252S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:169190006 G>T maps to NM_017631.5 T928T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr4:169294861 C>A maps to NM_001012967.1 S1577S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:1244356 C>A maps to NM_182632.2 S455S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:10256094 G>T maps to NM_012073.3 A120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:13792143 C>A maps to NM_001369.2 G2803*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:78573861 C>A maps to NM_152405.4 R388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:89953848 C>A maps to NM_032119.3 P1502P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:115827489 C>A maps to ENST00000257414 G161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:127625606 C>A maps to NM_001999.3 G2160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:131554244 G>T maps to NM_001142599.1 T25T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BQ-7060-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:137502366 G>T maps to NM_139199.1 T279T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:139682646 G>T maps to NM_002622.4 P4P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:140024234 C>A maps to ENST00000252100 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:140865819 C>A maps to NM_018928.2 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:141018585 C>A maps to NM_173828.4 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:147029918 G>T maps to NM_014790.3 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:148719568 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:149435802 G>T maps to NM_005211.3 S807S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:153065835 C>A maps to NM_001114183.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:154316728 C>A maps to NM_015465.3 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:171781009 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr5:176731045 C>A maps to NM_013237.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:10415175 C>A maps to ENST00000379613 E17*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:24563723 C>A maps to NM_014809.3 V818V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:30671005 C>A maps to NM_014641.2 G1914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:31914036 C>A maps to NM_001710.5 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:32809449 C>A maps to NM_148919.3 T200T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:33248490 C>A maps to NM_005452.5 G463G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:34392604 G>T maps to NM_001014.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:36790864 C>A maps to NM_020939.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:43111197 C>A maps to NM_002821.3 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:70970412 C>A maps to NM_001851.4 G466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:91263200 G>T maps to NM_145331.1 R238R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:110098158 G>T maps to NM_014845.5 L595L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:111913057 G>T maps to ENST00000340026 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:117686800 G>T maps to NM_002944.2 P972P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:135644392 G>T maps to NM_017651.4 R1079R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr6:145069621 C>A maps to NM_007124.2 S2727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:5342551 C>A maps to NM_153247.2 S525S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:44714851 G>T maps to ENST00000444676 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:48081006 C>A maps to ENST00000430738 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:55232971 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:82584364 C>A maps to NM_033026.5 S1968S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:99128902 C>A maps to NM_014569.3 P517P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:100173597 C>A maps to NM_002319.3 E558*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:102108795 C>A maps to NM_152892.1 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:113519997 G>T maps to NM_002711.3 S383S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:129770529 C>A maps to NM_014997.3 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:141755508 C>A maps to ENST00000475668 R1156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:141759705 G>T maps to ENST00000475668 R1333R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr7:149171567 G>T maps to NM_001163474.1 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:19818543 C>A maps to NM_000237.2 P424P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:20007238 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:21958381 C>A maps to NM_022749.5 T505T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:25296852 G>T maps to NM_017634.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:25365085 C>A maps to ENST00000434814 S969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:37993283 G>T maps to NM_004674.3 T573T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:67971610 C>A maps to NM_006837.2 S71S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:71069321 G>T maps to NM_006540.2 P426P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:114448921 C>A maps to NM_198123.1 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:144919430 C>A maps to NM_178564.3 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:144990823 C>A maps to NM_201380.2 E4526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr8:145150768 C>A maps to NM_001916.3 R55R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr9:730102 C>A maps to NM_015158.2 P917P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr9:26999701 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr9:32634481 G>T maps to NM_153809.2 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr9:35045130 C>A maps to NM_203299.2 P835P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr9:125239419 G>T maps to NM_001004451.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr9:130230037 C>A maps to NM_001005374.2 S183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr9:139652378 C>A maps to NM_178469.3 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr9:139874728 C>A maps to ENST00000224167 P215P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-BQ-7060-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr9:140140244 C>A maps to NM_001001710.1 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chr9:140970327 C>A maps to ENST00000277549 R1640R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:200941 C>A maps to NM_018390.3 R30R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:1561210 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:1746634 C>A maps to NM_001171038.1 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:18195782 A>T maps to NM_153346.4 I512I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:26212076 C>A maps to NM_173523.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:37664328 G>T maps to NM_000397.3 G408*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:44733230 A>T maps to NM_021140.2 K75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:53421808 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:63488802 C>A maps to NM_017677.3 G577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:63576179 G>T maps to NM_017677.3 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:69670487 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:80375288 C>A maps to NM_030763.2 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:86887408 C>A maps to NM_057162.2 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:103080543 G>T maps to NM_016370.2 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:117033239 C>A maps to NM_033495.3 V533V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:118151638 C>A maps to NM_001031855.1 R756R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7060-01A-11D-1961-08 chrX:152226588 C>A maps to NM_013364.4 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr1:65141615 C>A maps to ENST00000371073 C975*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr1:92712095 C>G maps to NM_053274.2 G592G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr10:101569943 C>T maps to NM_000392.3 D623D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:7046364 C>G maps to NM_001940.3 S645S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:57389325 G>A maps to NM_007264.3 L111L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:107154994 T>A maps to ENST00000357881 T661T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr12:130919338 G>A maps to NM_015347.4 D714D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr14:68232975 G>T maps to NM_015346.3 A1993A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr14:74058921 G>T maps to NM_152331.3 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:59501014 G>A maps to NM_004998.2 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:75968306 C>A maps to NM_001897.4 E2185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:79264260 G>A maps to NM_002891.4 R1226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:79748656 C>T maps to NM_015206.2 L56L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr15:94927308 C>A maps to NM_018349.3 T547T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr16:24226121 C>A maps to NM_002738.6 P669P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr16:67188575 G>T maps to NM_003789.3 T305T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr17:6375989 C>T maps to NM_031220.3 Q472Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr17:48474582 C>A maps to NM_018509.3 V32V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr18:21046216 G>T maps to NM_003831.3 E222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr19:8959622 C>A maps to NM_024690.2 L14503L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr19:35757259 A>G did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr19:36041736 C>A maps to NM_000704.2 G1026G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr19:36253152 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr19:42794069 G>T maps to NM_015125.3 G477G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr2:45233497 G>T maps to NM_016932.4 P229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr2:55771495 G>T maps to ENST00000339012 G331G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr2:69034459 C>A maps to NM_001007231.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr21:34014404 C>A maps to NM_003895.3 G1212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:52023048 G>C maps to ENST00000463937 L496L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:52651554 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr3:113377558 T>C maps to NM_001009899.2 S990S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr4:57190373 C>A maps to NM_020722.1 S1161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr4:77087447 C>A maps to NM_005506.2 T398T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr5:127685101 C>A maps to NM_001999.3 G976*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr5:158223436 C>A maps to NM_024007.3 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr6:35392131 A>C maps to NM_006238.4 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr6:54805943 C>A maps to NM_001010872.1 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr6:117706857 T>A maps to NM_002944.2 G764G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:43581575 T>A maps to NM_015052.3 V1409V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:79842141 A>G maps to NM_002069.5 K277K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:92147281 G>T maps to NM_000466.2 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr7:103029510 A>G maps to ENST00000354356 Y486Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr9:109691847 C>A maps to NM_021224.4 P1885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr9:114348297 C>A maps to NM_001146108.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chrX:64749563 C>A maps to NM_031206.4 E237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chrX:69637855 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chrX:142113806 G>T maps to ENST00000370504 E3*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr1:156737661 C>A maps to NM_005973.4 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr1:240371516 T>A maps to ENST00000406993 L1278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr10:33208865 A>G maps to ENST00000374956 P472P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr10:91177426 A>G maps to NM_012420.2 Q157Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr11:62489599 C>A maps to NM_001079559.1 E450*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr11:70333073 C>A maps to ENST00000338508 G1102G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr14:75470035 C>A maps to NM_014239.3 S74S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr15:102252161 C>A maps to NM_152334.2 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr16:4029167 G>A maps to NM_001116.3 P876P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr16:20787238 C>T maps to NM_005622.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr16:31195323 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr16:70711781 C>A maps to NM_138383.2 L215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr17:4575450 T>C maps to ENST00000301396 E1089E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr17:4908296 T>C did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr17:6946082 C>T did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr17:7506313 G>T maps to NM_004860.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr2:42483668 C>A maps to NM_019063.3 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr2:149799206 G>A maps to NM_004522.1 V174V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr20:37536821 G>T maps to NM_015568.2 E394*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr22:36055618 C>G maps to NM_030641.3 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr3:48459372 C>A maps to NM_001130082.1 T1107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr3:52432934 A>G maps to ENST00000273600 V4117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr5:121187825 G>T maps to NM_177478.1 R56R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr6:101296248 T>A maps to NM_006828.2 I192I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chr7:101988945 G>A maps to NM_001146210.1 L309L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chrX:24906188 C>A maps to ENST00000379068 R1372R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chrX:43515618 G>A maps to NM_000240.2 A10A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7062-01A-11D-1961-08 chrX:70367919 C>A maps to NM_181303.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:10177625 C>A maps to NM_001105562.2 R436R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:100214267 A>G maps to NM_001013660.2 Y19Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:110604110 G>T maps to NM_006492.2 P223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr1:157776892 G>A maps to NM_052938.4 A17A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr10:49667743 C>T maps to ENST00000417912 E230E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr10:70196868 A>C maps to NM_001080449.1 G601G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr11:208889 G>T maps to NM_021932.4 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr12:50869376 G>C maps to ENST00000429001 V641V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr16:71789971 C>T maps to ENST00000423132 E416E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr16:77325308 C>A maps to NM_199355.2 G1086*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr17:975900 C>A maps to NM_021962.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr17:34340314 G>A maps to NM_005064.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr17:66267172 A>G maps to NM_004694.4 F376F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr19:12088186 G>A maps to NM_001012753.1 G47G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:130738209 G>A maps to NM_032144.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:152512858 C>T maps to NM_001164507.1 E2101E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:166012355 G>T maps to NM_006922.3 Y363*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:167060899 C>T maps to ENST00000303354 K1492K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr2:179433842 G>C maps to NM_133378.4 Y23104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr20:5157343 C>A maps to NM_003818.2 Y114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr4:26426304 C>T maps to NM_005349.2 I242I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr5:121409740 G>T maps to NM_002317.5 Y334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr5:176831340 G>A maps to NM_000505.3 L292L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr6:28333713 G>A maps to NM_024493.2 E423E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr6:119282963 T>G maps to NM_024581.4 P1101P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5560-01A-01D-1589-08 chr8:105479133 C>T maps to NM_001385.2 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:11346094 G>C maps to NM_013319.2 L308L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:17609567 G>A maps to NM_016233.2 V663V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr1:27176924 G>A maps to NM_032283.2 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr11:128360460 A>T maps to NM_001143820.1 C75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr12:72288465 A>T maps to NM_022771.4 K237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr15:35044906 C>T maps to NM_020660.1 R246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr17:79495865 G>A maps to NM_001077182.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr19:2248400 G>A maps to NM_007165.4 S417S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr19:14677077 C>A did not map to a codon.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr2:24930396 G>A maps to NM_003743.4 R686R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr2:220338576 C>A maps to NM_005876.4 R1467R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr2:220437359 C>G maps to NM_002191.3 A88A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr22:32352659 C>T maps to NM_003405.3 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr3:47882519 C>A maps to NM_138615.2 R174R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr4:75937686 G>C maps to NM_015393.3 P32P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr7:139164444 C>T maps to NM_198508.2 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr9:22006243 G>A maps to NM_004936.3 V53V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-5561-01A-01D-1589-08 chr9:107531255 T>A maps to NM_018376.2 I128I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr1:32100954 C>A maps to NM_012392.3 G65*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr1:156843533 C>A maps to NM_002529.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr1:229631731 G>T maps to NM_018230.2 I294I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr10:104404880 C>T maps to NM_030912.2 Y169Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr12:48137415 C>A maps to NM_001098531.2 L574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr12:49743365 T>C maps to NM_024902.2 L237L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr14:67848334 T>C maps to NM_004094.4 Y202Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr16:4431957 C>A maps to NM_138440.2 T360T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr16:50707451 G>T maps to NM_182854.2 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:18212207 A>G maps to NM_004618.3 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:44845985 C>T maps to NM_030753.3 V256V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr17:78321575 C>T maps to NM_020914.4 R3196R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr18:65181491 A>G maps to NM_032160.2 N128N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr19:39905977 G>T did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr19:40478460 A>G maps to NM_006503.2 T107T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr19:58805587 G>A maps to NM_021089.2 G138G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr2:15691632 A>G maps to NM_015909.2 I121I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr2:112615902 T>C maps to NM_022662.2 V446V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr2:220150707 G>T did not map to a codon.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr20:56227615 C>T maps to NM_020182.3 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr20:61468579 C>T maps to NM_001853.3 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr21:16337669 A>G maps to NM_003489.3 D948D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr21:22658661 A>T maps to NM_004540.2 R137R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr22:18021910 C>T maps to ENST00000400579 C672C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr22:29656764 C>A maps to NM_012265.1 G207G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr3:9974672 C>A maps to NM_153461.2 S591*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr3:109023470 T>C maps to NM_138815.3 T235T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr4:147561257 T>C maps to NM_004575.2 H176H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr4:169433374 G>A maps to NM_001166108.1 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr6:45390465 A>G maps to ENST00000359524 Q133Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr8:10390472 G>A maps to NM_198464.3 W219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr8:142148127 G>T maps to NM_014957.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7834-01A-11D-2136-08 chr9:127262608 C>A maps to NM_004959.4 P210P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr1:10714013 C>A maps to NM_001079843.1 S700S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr1:31465391 C>A maps to ENST00000373741 E371*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr1:109811763 G>T maps to NM_001408.2 G2222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr1:156848916 C>A maps to NM_002529.3 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr1:209948729 G>T maps to NM_025228.2 E271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr1:224482024 C>A maps to NM_002533.2 A423A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr1:226421110 G>T maps to ENST00000366807 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr1:237806688 C>A maps to NM_001035.2 P2428P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DW-7837-01A-11D-2136-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr10:94264638 C>A maps to NM_004969.3 E448*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:9161267 C>A maps to NM_015213.2 E1272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:61058748 C>A maps to NM_152718.2 G94G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:62434312 G>T maps to NM_001043229.1 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:62752129 C>A maps to NM_004790.3 G11G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:67223892 C>A maps to NM_145200.3 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:73066675 C>G maps to NM_014786.3 A1184A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:74800092 G>T maps to NM_001005285.1 S222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:108536011 C>A maps to NM_004398.2 P44P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr11:124620610 C>A maps to NM_014312.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr12:7244122 C>A maps to ENST00000290575 T66T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr12:31579295 G>T maps to NM_144973.3 L723L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr12:119583349 C>A maps to NM_194286.2 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr13:113728834 G>A maps to NM_001112732.1 E415E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr14:21624077 G>T maps to NM_001004731.1 S36*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr15:34355211 C>A maps to NM_012125.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr15:42143315 C>A maps to ENST00000320955 T3592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr15:67692529 C>A maps to NM_001031715.2 R662R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr16:716910 G>T maps to NM_145294.4 E1671*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr16:1962127 G>T maps to ENST00000454677 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr16:2213980 C>A maps to NM_032271.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr16:3169443 G>T maps to NM_001042428.1 P261P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr16:4861191 G>T maps to NM_032569.3 P522P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr16:53301950 C>A maps to ENST00000219084 R1544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr17:3421950 G>T maps to ENST00000381913 L668L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr17:9536334 C>A maps to NM_145054.4 G435G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr17:25924418 C>A maps to ENST00000268763 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr17:37826557 C>A maps to NM_002686.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr17:42992788 C>A maps to NM_002055.3 V22V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr17:71427749 C>A maps to NM_001144952.1 S457S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr17:73237564 G>T maps to NM_138619.2 R288R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr17:80053199 G>A maps to NM_004104.4 D92D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr18:28588038 C>A maps to NM_001941.3 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr18:56963930 C>A maps to NM_181654.3 *161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr18:63477229 C>A maps to NM_004361.2 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr18:77513769 G>T maps to NM_004715.3 E956*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:16989424 G>T maps to NM_015260.1 E1126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:17941407 C>A maps to NM_000215.3 S1000S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:36431040 C>A maps to NM_024509.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:46094973 C>A maps to NM_005282.2 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:47763865 C>A maps to NM_015603.2 R78R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:55526340 C>A maps to NM_001083899.1 R324R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:56539071 C>T maps to NM_153447.4 V491V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:1497622 C>A maps to NM_000547.5 P606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:27685656 C>A maps to NM_015662.1 G676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:63282996 C>A maps to NM_014562.3 S204*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:71607357 G>T maps to NM_014497.3 E758*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:86067446 C>A maps to NM_003896.3 A359A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:125521356 C>A maps to NM_130773.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:128262664 G>T maps to NM_017969.2 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:133547604 G>T maps to NM_207363.2 L361L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:136103189 C>A maps to NM_032143.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:136719006 C>A maps to NM_001349.2 V93V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:175213592 G>T maps to NM_004882.3 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:180309602 T>A maps to NM_152520.4 A399A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr20:3678717 C>A maps to NM_023068.3 G617*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr20:35128760 C>A maps to ENST00000339266 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr20:36952336 C>A maps to NM_001725.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr20:62078165 G>C maps to NM_172107.2 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr20:62187069 C>A maps to NM_024059.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr22:29611566 C>A maps to NM_133455.2 T89T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr22:30185132 G>T maps to NM_032204.3 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr3:15516976 C>A maps to NM_005677.3 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr3:17053417 C>A maps to NM_001144382.1 P856P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr3:49694716 G>T maps to NM_003458.3 V2576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr3:52183865 G>T maps to NM_015426.4 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr3:126724051 C>A maps to NM_032242.3 S621S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr3:184105760 C>A maps to NM_003741.2 R832R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr3:186389554 C>A maps to NM_000412.2 R179R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr4:10492132 G>T maps to NM_052964.2 L415L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr4:49063891 C>A maps to NM_025087.2 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr5:32364062 G>T maps to NM_016107.3 S1012S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr5:41904492 G>T maps to NM_175921.4 V8V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr5:56177036 T>A maps to NM_005921.1 P769P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr5:79086846 C>A maps to NM_153610.3 S3915*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr5:140856301 G>T maps to NM_002588.2 E207*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr6:37138953 G>T maps to ENST00000373507 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr6:56357878 C>A maps to ENST00000361203 L6590L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr7:138145433 G>A maps to NM_015905.2 A47A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr7:141341085 G>T maps to NM_018238.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr8:92365154 G>T maps to NM_134266.1 V415V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr8:139638440 C>A maps to NM_152888.1 G1237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr8:144889174 G>T maps to NM_182706.3 L729L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr8:145113509 G>T maps to ENST00000360660 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr9:19080660 C>A maps to NM_017645.3 G294*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr9:116346545 C>A maps to NM_144488.4 R952R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr9:117266835 C>A maps to NM_015404.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr9:130501982 G>T maps to NM_170600.2 T795T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr9:133759488 C>A maps to NM_007313.2 I623I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chrX:54470968 C>A maps to NM_058163.1 R188R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chrX:74698770 G>T maps to NM_144969.2 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chrX:100492627 C>A maps to NM_001939.2 S101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chrX:120008753 G>T maps to NM_001145718.1 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chrX:135291545 C>A maps to NM_001159702.2 S278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chrX:135790925 C>A maps to NM_004840.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr1:10535060 T>C did not map to a codon.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr1:145561664 C>T maps to NM_144698.3 T451T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr10:71906009 C>G maps to NM_173555.2 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr10:99222419 C>T maps to ENST00000422291 L665L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr11:67412338 A>G maps to NM_080658.1 G212G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr12:14613822 C>T maps to NM_018179.3 P851P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr14:64633997 G>A maps to NM_182914.2 L5551L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr16:51172850 A>G maps to ENST00000251020 H1094H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr16:58713826 C>T maps to NM_018231.1 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:3919675 C>A maps to NM_015113.3 G2696*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:4995908 T>C maps to NM_153018.2 C370C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr17:38420805 A>G maps to NM_133264.4 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:10471913 G>A maps to ENST00000423585 Q261Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:14105674 T>C maps to NM_145287.3 G288G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:21451429 G>T maps to ENST00000416669 V1603V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr18:22805628 G>C maps to NM_015461.2 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr19:48863336 G>T maps to NM_018273.2 R121R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr19:50550198 G>T maps to NM_015428.1 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:74761482 G>A maps to NM_032603.2 H633H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:132236968 G>A maps to NM_080386.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr2:241516156 C>T maps to NM_018226.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr20:62374340 T>C maps to NM_020062.3 *388Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr3:47456624 C>T maps to NM_012235.2 L1034L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr3:184922366 G>A maps to NM_001966.3 I249I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr4:6066675 C>T maps to NM_001099433.1 L454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr6:138727186 C>A maps to NM_014320.2 T106T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:39446254 C>T maps to NM_007252.3 S314S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:44805817 C>G maps to NM_031449.3 P766P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:87051486 A>G maps to NM_018849.2 L756L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:129962494 T>C maps to NM_016352.3 H415H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr7:134260619 C>T maps to ENST00000418096 C246C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr9:93606497 C>A maps to NM_003177.5 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr9:115973832 A>G maps to ENST00000446284 A56A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr9:128001453 A>G maps to NM_005347.4 G254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chrX:41200809 T>C maps to NM_001356.3 R75R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr11:723295 C>A maps to NM_022772.3 S466*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr11:58940187 G>T maps to NM_015177.1 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr12:27787952 T>C maps to NM_003622.3 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr19:21720165 C>A maps to NM_001001415.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr2:73827934 T>C maps to NM_015120.4 R3932R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr3:73673577 G>C maps to NM_015009.1 A133A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr6:43044270 T>G maps to NM_002821.3 P15P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:20824952 G>C maps to NM_182700.4 G161G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:20824955 C>G maps to NM_182700.4 G160G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:107204286 C>A maps to NM_006348.3 G50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr7:141731532 T>G maps to ENST00000475668 V508V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr8:3165918 C>A maps to NM_033225.5 P1246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr1:21546591 G>C maps to NM_001397.2 S723S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr1:210267874 T>C maps to NM_001146261.1 S262S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:24835171 T>C maps to NM_019590.3 H1917H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:28270469 T>C maps to NM_018076.2 K287K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr10:35324144 G>T maps to NM_001198778.1 I338I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr11:43905564 T>C maps to NM_139178.3 I72I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr11:66613412 A>C maps to NM_005133.2 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:100048988 C>G did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:104378525 G>T did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:124829473 G>A maps to NM_006312.4 T1468T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr12:133235891 A>G maps to ENST00000455752 P1091P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr15:65223119 T>G did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr15:65684504 T>A maps to NM_020962.1 K697*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr16:2142547 G>A maps to NM_001009944.2 Y3734Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr17:7470322 G>A did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr17:10312635 A>T maps to NM_002472.2 T619T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr19:7083598 T>C maps to NM_024341.2 S379S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr2:61493233 C>T maps to NM_014709.3 K1834K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr2:218713667 C>G maps to NM_022648.4 T399T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr21:46117130 C>T maps to NM_198699.1 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr22:29445938 C>G maps to NM_032173.2 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr3:127396050 C>A maps to NM_172027.2 I228I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr4:79786782 T>C maps to NM_198892.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr5:140605206 G>C maps to NM_018934.2 A710A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr5:172659919 C>G maps to NM_004387.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr6:32191690 T>C maps to NM_004557.3 S5S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr6:33141943 G>T maps to NM_080680.2 R828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr6:161470013 C>A maps to NM_005922.2 S237*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr7:1589782 G>A maps to NM_001097620.1 I176I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr9:33796656 C>T maps to NM_007343.3 D76D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr9:134404930 G>A maps to NM_031432.2 N103N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chrX:16804660 A>G maps to NM_018360.2 E17E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chrX:19626145 G>T maps to NM_031892.2 G305G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chrX:30261229 C>A maps to NM_002367.3 G326G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chrX:91456391 C>T maps to NM_032968.3 R1018*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr1:11710790 C>G maps to NM_012168.4 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr1:224302058 C>G maps to NM_015176.2 L76L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr12:103352210 G>C maps to NM_004316.3 A63A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr12:112942599 G>T did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr12:122618011 C>A maps to NM_014938.3 R404R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr13:41767952 G>A maps to NM_032138.4 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr15:73045221 C>A maps to NM_031284.4 A317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr17:4575081 C>T maps to ENST00000301396 E1212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr17:27052950 G>T maps to NM_138463.3 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr19:971935 C>G maps to NM_005224.2 G551G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr19:58867602 C>A maps to NM_198458.1 E467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr2:44207046 A>G maps to NM_133259.3 S129S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr22:42154471 A>C maps to NM_152513.3 G685G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr3:48510781 C>T maps to NM_016479.3 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:80600584 G>A maps to NM_032280.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:140753887 C>T maps to NM_018919.2 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr5:159520918 G>A maps to NM_001130864.1 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr6:35436590 C>T maps to NM_007104.4 R7R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr7:26251699 A>T did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr8:124787417 C>A maps to NM_144963.2 Y63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr9:136216908 T>A did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr1:94054977 T>C did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr1:160181402 C>A maps to ENST00000368075 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr1:197684158 A>G did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr11:76890089 G>T did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr11:134115447 C>T maps to NM_052875.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr16:2168071 G>A maps to NM_001009944.2 F307F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr17:45727755 G>A maps to NM_002265.4 R15R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr19:5897009 T>A did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr19:31770236 A>G maps to NM_020856.2 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr2:234173558 T>C maps to ENST00000392018 T137T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr3:14724702 G>T maps to NM_032137.4 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr9:114429093 G>A did not map to a codon.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:26608864 A>G maps to NM_183008.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:53362194 T>C maps to ENST00000371522 K292K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr1:185060811 T>C maps to NM_007212.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr12:88471485 G>T maps to NM_025114.3 T1858T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr13:100623584 C>T maps to NM_033132.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr16:85010784 G>A maps to NM_001145548.1 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr17:79504051 C>A maps to NM_001077182.2 G499G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr2:42990998 C>A maps to NM_148962.4 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr20:47258947 G>A maps to NM_020820.3 N1227N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr22:38822919 A>C maps to NM_152868.1 G406G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr3:132418234 A>T maps to ENST00000393156 I649I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr6:111701284 C>A maps to NM_002912.3 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr6:160769795 C>T maps to ENST00000392145 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr7:99707630 G>A maps to ENST00000472509 D465D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr8:21974549 C>T maps to NM_005144.4 V1072V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7963-01B-11D-A28G-10 chr8:27099959 G>A maps to NM_030795.2 S21S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:23408750 C>A maps to NM_001009999.2 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:26672964 C>A maps to NM_001039775.3 E62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:27223979 G>T maps to NM_022078.2 R230R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:110740837 C>A maps to NM_001010898.2 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:111216741 G>T maps to NM_002232.3 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:150484048 C>A maps to ENST00000369049 P302P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:157659672 C>A maps to NM_052939.3 A575A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:203151980 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:203276256 C>A maps to NM_006763.2 P56P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:220330641 G>T maps to ENST00000358951 T1175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:228465013 G>T maps to NM_001098623.1 G2252*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:229625839 C>A maps to NM_018230.2 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr1:229772876 C>A maps to NM_014777.2 P839P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr10:15172175 C>A maps to ENST00000378143 A316A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr10:69882001 C>A maps to NM_032578.2 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr10:73447475 G>T maps to ENST00000398860 G692*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr10:95372754 C>A maps to NM_006204.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr10:101294790 G>T maps to NM_145285.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr10:104377121 G>T maps to NM_016169.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:1099776 T>C maps to ENST00000441003 P2458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:2191068 G>T maps to NM_199292.2 L72L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:7686646 C>A maps to NM_016229.3 L263L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:14901681 C>A maps to NM_024514.4 G334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:14990449 G>T maps to NM_001741.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:18158841 G>T maps to NM_054031.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:46726995 C>A maps to NM_024741.2 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:57427403 G>T maps to NM_006831.2 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:62373389 C>A maps to ENST00000278845 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:68517723 C>A maps to NM_004923.3 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:70281766 G>T maps to NM_001184740.1 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:73589859 C>A maps to NM_025155.1 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:86663407 G>T maps to NM_012193.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:99941279 C>A maps to NM_014361.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:103062344 G>T maps to NM_001080463.1 G2513*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr11:129306842 C>A maps to NM_003658.4 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:9000290 C>T maps to NM_144670.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:21958182 C>A maps to NM_005691.2 V1525V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:31242079 C>A maps to NM_030653.3 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:53291346 C>A maps to NM_002273.3 L439L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:53664226 C>A maps to NM_012291.4 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:53722034 C>A maps to NM_001173467.1 T397T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:56847389 C>A maps to NM_012064.3 L170L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:64174891 T>G maps to NM_014254.1 L88*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:81545642 G>T maps to NM_024560.2 G314G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:102069085 C>A maps to NM_002465.2 P942P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:111052112 G>T maps to NM_001082538.2 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:125436981 C>A maps to NM_032656.3 E944*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:129559034 G>T maps to NM_133448.2 P895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:132497610 C>A maps to ENST00000333577 R1203R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr12:132551452 C>A maps to ENST00000333577 T2932T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr13:52548698 C>A maps to NM_000053.2 L219L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr13:101717913 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr14:50750751 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr14:51223237 C>A maps to NM_020921.3 E1504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr14:53417244 C>A maps to NM_001134999.1 A14A. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr14:58937415 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr14:58954746 C>A maps to ENST00000354386 P1202P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr14:64518895 C>A maps to NM_182914.2 P2755P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr14:91681776 G>T maps to NM_001102368.1 L531L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr14:91776234 C>G maps to NM_001080414.2 L944L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr14:97010484 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr15:39885649 C>A maps to NM_003246.2 T1016T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr15:48056478 C>A maps to NM_153618.1 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr15:59323599 G>T maps to ENST00000434298 S193S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr15:75341027 C>A maps to NM_021823.3 P165P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr15:75648294 G>T maps to NM_006715.2 P1025P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr15:85366587 C>A maps to NM_020778.4 P259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr15:89866112 C>A maps to NM_002693.2 V762V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr16:701025 C>A maps to NM_145294.4 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr16:3304235 G>T maps to NM_000243.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr16:31374025 C>A maps to NM_000887.3 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr16:51174904 C>A maps to ENST00000251020 G410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr16:58568272 G>T maps to NM_016284.3 T1891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr16:66612902 G>A maps to NM_052999.3 *287*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr16:67997379 C>A maps to NM_005072.4 L66L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:4075869 C>A maps to NM_016376.3 P1041P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:5039137 C>A maps to NM_004505.2 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:7250423 G>T maps to NM_014716.3 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:7496056 C>A maps to NM_004860.3 G562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:18925361 C>A maps to NM_006613.3 L188L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:26851840 C>A maps to NM_003593.2 S148S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:26958904 C>A maps to NM_014680.2 R1343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:34958367 G>T maps to NM_024864.3 L43L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:35506853 C>A maps to NM_198834.1 L1871L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:59853829 C>A maps to NM_032043.2 G677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:73808534 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:73845688 C>A maps to NM_012478.3 A100A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:74081471 C>A maps to NM_001145297.2 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:78163554 G>T maps to NM_024110.2 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:79165050 G>T maps to ENST00000269392 R906R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:79167916 G>T maps to ENST00000269392 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:80085763 C>A maps to ENST00000445854 T790T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr17:80405454 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr18:2951267 C>A maps to NM_014646.2 S125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr18:21137134 C>A maps to NM_000271.4 E301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr18:61060701 G>T maps to NM_004869.3 A391A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr18:61647067 C>A maps to NM_198833.1 R68R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:1295691 G>T maps to NM_001405.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:2434027 G>T maps to NM_032737.2 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:5664152 C>A maps to ENST00000433404 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:5664161 G>T maps to ENST00000433404 S761S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:8654434 C>A maps to NM_030957.2 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:9071965 C>A maps to NM_024690.2 V5160V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:9091598 C>A maps to NM_024690.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:10886520 C>A maps to NM_001005361.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:14029607 C>A maps to NM_017721.4 P332P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:14067328 C>A maps to NM_138353.2 S260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:15079169 G>T maps to NM_005071.1 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:15299866 C>A maps to NM_000435.2 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:19344661 C>A maps to NM_004386.2 T1028T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:38857809 G>T maps to NM_021185.4 V876V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:50339643 C>A maps to NM_030973.3 P709P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:51379946 C>A maps to NM_005551.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:54692132 G>T maps to NM_024298.3 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:55107774 G>T maps to NM_006863.1 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr19:55176623 C>A maps to ENST00000391733 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:55473594 G>A maps to NM_002453.2 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:69754451 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:71058331 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:85982002 C>A maps to NM_032827.6 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:138738945 C>A maps to NM_001024075.1 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:207171573 G>A maps to NM_020923.1 R774R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:232393416 C>A maps to NM_006056.4 S105S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:237103571 G>T maps to NM_212556.2 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr2:238289654 G>T maps to NM_004369.3 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr20:2641011 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr20:20493665 C>A maps to NM_020343.3 G1449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr20:57829581 C>A maps to NM_178457.1 P1606P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr20:61513023 G>T maps to NM_033081.2 P1428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr21:41711298 C>A maps to NM_001389.3 V418V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr21:45733862 G>T maps to NM_002626.4 E236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr21:46057372 C>T maps to NM_181688.1 C13C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr22:19226878 C>A maps to NM_007098.3 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr22:20843368 G>T maps to NM_032775.3 R44R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr22:38318112 C>A maps to NM_033386.2 S235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr22:50617408 C>A maps to NM_052839.3 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr22:50719553 C>A maps to NM_012401.2 E1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:4836870 G>T maps to ENST00000356617 G2309*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:9798523 C>A maps to NM_016819.3 P324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:12983241 C>A maps to ENST00000429247 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:25770622 C>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:32932840 G>A maps to NM_001039111.1 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:38941491 G>T maps to ENST00000302328 R639R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:53894169 G>T maps to NM_018725.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:113286455 G>T maps to ENST00000393830 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:122287652 C>A maps to NM_138287.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:122414426 C>A maps to NM_017554.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:155485335 C>A maps to ENST00000340171 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:183508601 C>A maps to NM_018023.4 P977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:186970995 C>A maps to NM_139125.3 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr3:197241146 G>T maps to NM_203315.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:1729758 C>A maps to NM_006342.1 S210S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:2733529 C>A maps to ENST00000324666 R1245R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:3076695 T>G maps to NM_002111.6 P48P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:39293380 C>A maps to ENST00000381897 G1017*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:87691258 C>T maps to NM_080685.2 V1575V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:123664441 G>T maps to NM_152618.2 V465V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:174225145 G>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:174450050 G>T maps to NM_021973.2 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:184210637 C>A maps to ENST00000448232 T1102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr4:186084071 G>T maps to NM_020827.1 S493S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:6600059 C>A maps to NM_017755.5 A761A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:9052128 C>A maps to NM_003966.2 E901*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:95115954 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:139235322 C>A maps to NM_013982.2 T418T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:140202016 C>A maps to NM_018908.2 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:141233695 C>A maps to NM_032420.2 E1209*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:149751576 C>A maps to ENST00000451292 P216P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:156022060 G>T maps to NM_000337.5 G168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:159781880 G>A maps to NM_031908.4 G91G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:180048685 C>A maps to NM_182925.4 E626*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr6:10402727 C>A maps to ENST00000379613 E296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr6:33134568 C>A maps to NM_080680.2 P1422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr6:33144768 C>A maps to NM_080680.2 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr6:34498130 C>A maps to NM_020804.3 P300P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr6:46979744 C>A maps to ENST00000283297 E373*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr6:107908318 C>A maps to NM_018013.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr6:119222018 C>A maps to NM_014034.2 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr6:151121857 C>A maps to NM_001029884.1 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr7:2418388 C>A maps to ENST00000314800 S740S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr7:21470438 C>A maps to NM_003112.3 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr7:45115565 C>A maps to NM_001029835.2 P436P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr7:98562315 C>A maps to ENST00000359863 S2291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr8:3166025 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr8:29035077 C>A maps to NM_015254.3 V246V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr8:30694448 T>C maps to NM_031271.3 Q2734Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr8:38173062 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr8:98943499 C>A maps to ENST00000254898 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr8:103663763 C>A maps to NM_005655.2 G266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr8:144896013 C>A maps to NM_182706.3 A110A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr8:144997448 G>T maps to NM_201380.2 A2353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr9:37033997 G>T maps to NM_016734.1 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr9:37733795 G>T maps to NM_014907.2 G398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr9:101006349 C>A maps to NM_018421.3 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr9:134505711 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr9:139299145 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chrX:9864374 C>A maps to NM_001649.2 P809P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chrX:16168748 C>A maps to NM_005314.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chrX:53246991 C>A maps to NM_004187.3 G170*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chrX:100880621 C>A maps to NM_016607.3 S218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chrX:105449719 G>T maps to NM_001171020.1 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chrX:106185447 C>A maps to NM_024657.4 E794*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:7811381 C>A maps to NM_015215.2 R1605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:11907409 C>A maps to NM_006172.3 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:12368653 C>A maps to NM_015378.2 T2202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:16271010 C>A maps to ENST00000375733 S385S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:16375508 G>T maps to NM_001165945.1 G15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:19492229 C>A maps to ENST00000375267 L1377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:21212813 G>T maps to NM_001198801.1 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:27739178 A>G maps to NM_006990.2 C237C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:28477208 C>A maps to NM_001164721.1 L108L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:31215371 C>A maps to NM_006762.2 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:36028145 G>T maps to NM_001014839.1 E433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:36808979 C>A maps to ENST00000373130 A363A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:37941291 C>A maps to NM_025079.2 I65I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:39888511 C>T maps to ENST00000361689 A3301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:44054577 G>T maps to NM_002840.3 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:45269305 C>A maps to NM_004073.2 S369S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:45270382 C>A maps to NM_004073.2 R523R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:53262038 T>C maps to NM_024646.2 A470A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:82432163 G>T maps to ENST00000370717 L736L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:85462548 G>T maps to NM_153259.2 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:91404116 C>A maps to NM_201269.1 E932*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:94037262 G>T maps to NM_003567.2 S646S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:94522329 A>G maps to NM_000350.2 L737L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:115276478 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:156821561 G>A maps to NM_014215.2 C320C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:160786474 G>T maps to ENST00000263285 G388G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:181767828 C>A maps to ENST00000357570 G2267G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:190067482 G>T maps to NM_199051.1 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:204092873 G>T maps to ENST00000367206 R450R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:206329026 C>A maps to ENST00000361052 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:207106512 T>C did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:231342466 C>A maps to NM_001004342.3 R584R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr10:35896560 G>T maps to NM_153368.2 A40A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr10:76857614 G>T maps to ENST00000356369 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr10:81063805 G>T maps to NM_020338.3 S720S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr10:101645598 C>A maps to ENST00000342239 G1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr10:102242539 G>T maps to NM_003393.3 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr10:115413821 G>T maps to ENST00000369358 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:373762 C>A maps to NM_178537.4 R240R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:607576 C>A maps to ENST00000264555 P707P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:9519249 T>G maps to NM_003442.5 T290T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:18751079 G>T maps to NM_032781.3 A508A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:46890253 G>T maps to ENST00000256991 A1661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:47317126 C>A maps to NM_003682.3 T1199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:47469614 C>A maps to NM_005055.3 E94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:57574385 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:61503082 G>T maps to NM_006133.2 V393V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:62341308 C>A maps to NM_001404.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:66453548 C>A maps to NM_006946.2 V2322V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:68747837 C>A maps to NM_198923.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:70279367 G>T maps to NM_001184740.1 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:72292462 G>T maps to NM_002599.3 A661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:73068316 C>A maps to NM_014786.3 A1344A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:76371567 G>T maps to NM_001128922.1 R357R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:82879860 G>T maps to NM_015885.3 V828V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:104820398 C>A maps to NM_001225.3 G218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:117869794 G>T maps to NM_001558.3 G392G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:118452032 C>A maps to ENST00000359415 R67R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:119044725 G>T maps to NM_024618.2 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:119182854 G>T maps to NM_006500.2 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:133795704 C>A maps to NM_014987.1 E655*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:134162057 C>A maps to NM_001080407.2 L254L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr11:134254002 C>A maps to NM_054025.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:8242577 C>A maps to NM_015509.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:9265069 G>T maps to NM_000014.4 T111T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:43887002 C>A maps to ENST00000389420 V307V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:54379723 C>A maps to NM_017409.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:56579997 C>A maps to NM_003075.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:56995524 C>A maps to NM_013449.3 P1294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:64615969 C>A maps to ENST00000311915 A16A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:65461549 G>T maps to NM_007191.4 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:66546127 C>A maps to ENST00000286424 G126*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:66935659 C>A maps to ENST00000359742 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:95603625 A>G maps to NM_018351.3 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:96273431 G>A maps to NM_182496.2 Q378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:106715286 C>A maps to NM_152772.1 P146P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:110224603 G>T maps to NM_021625.4 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr12:129299549 C>A maps to ENST00000376744 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr13:38237840 G>T maps to NM_003306.1 S467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr13:50115836 G>A maps to NM_018191.3 V433V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr13:93518679 C>A maps to NM_004466.4 P569P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr13:95271584 G>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr13:101997638 G>T maps to NM_052867.2 G259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:20757896 G>T maps to NM_138376.2 S404S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:20845912 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:23310764 C>A maps to NM_004995.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:23853814 C>A maps to NM_002471.3 E1801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:30066927 C>A maps to NM_002742.2 G735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:50796824 G>T maps to NM_004196.3 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:56079009 C>A maps to NM_001079521.1 R82R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:57710920 C>A maps to ENST00000340918 G143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:64727167 G>T maps to NM_001437.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:69704354 C>A maps to NM_001193363.1 S452S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:77691765 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:91763663 C>A maps to NM_001080414.2 L1317L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:92909055 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:95669336 G>T maps to NM_024734.3 S783S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:97342416 G>T maps to NM_003384.2 T373T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:100607531 G>T maps to NM_016337.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr14:105618365 G>T maps to NM_002226.3 P316P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr15:31295131 C>A maps to NM_002420.4 A1235A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr15:33993202 C>A maps to NM_001036.3 T2135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr15:40662074 G>T maps to NM_033510.1 G1254G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr15:50593091 C>A maps to NM_005254.5 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr15:56216897 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr15:64067420 C>A maps to ENST00000261887 P134P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr15:65347298 G>T maps to NM_016563.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr15:99465472 C>A maps to NM_000875.3 T766T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr15:101454974 C>A maps to NM_000693.2 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:103499 G>T maps to NM_016310.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:138841 G>T maps to ENST00000399953 S466S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:16225743 G>T maps to ENST00000399408 L1316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:17353016 G>T maps to NM_022166.3 P247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:27523217 G>T maps to NM_001520.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:28913549 G>T maps to NM_173201.3 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:29851665 C>A maps to NM_017458.3 I359I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:31091065 G>T maps to NM_014699.3 E1141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:49670137 G>T maps to NM_015069.2 T975T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:67270509 G>T maps to NM_013241.2 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:70693537 C>A maps to NM_152456.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr16:89349904 G>T maps to NM_013275.4 P1015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:4085567 G>T maps to NM_016376.3 R678R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:4638591 G>T maps to NM_001100812.1 T190T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:7290441 C>A maps to NM_003985.3 R456R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:37340025 G>T maps to NM_000723.3 A330A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:38572682 C>A maps to ENST00000357601 E87*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:39645954 C>A maps to NM_003771.4 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:40966021 G>T maps to NM_003766.3 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:41006666 G>T maps to NM_003734.2 R601R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:42284928 C>A maps to NM_014233.2 E688*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:42851903 G>T maps to NM_002390.4 L374L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:46152377 G>A maps to ENST00000442683 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:48267364 G>T maps to NM_000088.3 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:48676928 G>T maps to NM_018896.3 S1133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:56584103 C>A maps to NM_004687.4 E331*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:63526177 C>A maps to NM_004655.3 A816A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:73914057 G>T maps to ENST00000389570 S766S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:74934149 C>A maps to NM_198955.1 P512P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:76133811 C>T maps to NM_152468.4 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:78313947 C>A maps to NM_020914.4 V1976V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:79539114 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr17:79612400 G>T maps to NM_031945.3 L140L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr18:580533 G>T maps to NM_004066.1 V42V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr18:55103901 C>A maps to NM_004852.2 S318S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr18:72186229 C>A maps to NM_018235.2 P419P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:868114 C>A maps to NM_005481.2 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:1811651 C>A maps to NM_138813.2 T28T. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:4508944 G>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:5208354 C>A maps to NM_002850.3 P1845P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:8176049 C>A maps to NM_032447.3 E1368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:11233959 C>A maps to NM_000527.4 R751R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:11338051 C>A maps to ENST00000319867 V972V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:13873689 C>A maps to NM_030818.2 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:22272218 C>A maps to NM_033468.2 S556*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:35504492 C>A maps to NM_020895.3 S256S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:35940918 G>T maps to NM_005306.2 A101A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:36221256 C>A maps to NM_014727.1 P1697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:36348059 C>A maps to NM_199180.2 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:36394710 C>A maps to NM_014266.3 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:36398134 G>T maps to NM_003332.3 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:42814876 C>A maps to NM_199285.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:42907052 G>A maps to NM_005357.2 T891T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:43689023 G>T maps to ENST00000270059 R114R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:44570871 C>T maps to NM_013361.4 F297F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:46282774 C>A maps to NM_004409.3 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:48950072 C>A maps to NM_031485.3 P147P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:49950352 A>G maps to NM_017916.2 P205P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:54682543 C>A maps to NM_024298.3 T323T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:54937847 A>G did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:55377852 G>T maps to ENST00000355608 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr19:55686674 C>A maps to NM_003180.2 L191L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:16746918 G>T maps to NM_030797.3 R63R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:28634918 C>A maps to NM_005253.3 P195P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:85570831 C>A maps to NM_017750.3 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:99181107 C>A maps to NM_001134224.1 T683T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:101893716 C>A maps to NM_173647.3 G396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:102448265 G>T maps to NM_145686.2 E198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:112608403 A>G maps to NM_022662.2 D533D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:122120774 C>A maps to NM_015282.2 L1393L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:135883801 G>T maps to NM_001172435.1 V294V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:152315421 G>T maps to NM_018151.4 G985*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:158178157 C>A maps to NM_001009959.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:158971749 C>A maps to NM_001135098.1 T163T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:159389785 C>A maps to NM_003628.3 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:179477040 G>T maps to NM_133378.4 T14169T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:189916188 C>A maps to NM_000393.3 G930*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:204193287 G>T maps to ENST00000295851 R17R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:206590748 C>A maps to NM_201266.1 L311L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:218678432 T>A maps to NM_022648.4 P1508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:219920489 C>A maps to NM_002181.3 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:230693995 C>A maps to ENST00000389044 E455*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:240002885 C>A maps to NM_006037.3 V880V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:241536255 C>A maps to NM_023083.3 S547*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:242403322 C>A maps to NM_014808.2 P607P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr20:16492084 G>T maps to NM_024704.4 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr20:19261601 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr20:35128632 C>A maps to ENST00000339266 R711R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr20:44050123 C>A maps to NM_015937.4 R379R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr20:47741018 T>A maps to NM_017453.2 K239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr20:60895641 C>A maps to NM_005560.3 G2244G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr20:61522480 G>T maps to NM_033081.2 P1124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr20:61950472 C>A maps to ENST00000326996 P916P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr21:33671356 C>A maps to ENST00000445271 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr22:17688127 C>A maps to NM_017424.2 V125V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr22:18022265 C>A maps to ENST00000400579 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr22:20302894 C>A maps to NM_033257.3 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr22:20761209 C>A maps to NM_003426.2 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr22:21105591 C>A maps to NM_058004.2 E990*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr22:31523509 G>T maps to ENST00000331075 L593L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr22:37453436 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr22:38823294 C>A maps to NM_152868.1 S281S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr22:50217235 C>A maps to ENST00000342989 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:9512466 G>T maps to ENST00000407969 G1036*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:9792854 G>T maps to NM_016821.2 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:52437732 C>A maps to NM_004656.2 V476V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:52537075 C>A maps to NM_015136.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:108407565 G>T maps to NM_014648.3 E1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:121208970 G>T maps to ENST00000393672 S1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:125282592 C>A maps to NM_022776.4 P321P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:182870221 G>T maps to NM_014398.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:184038755 C>A maps to NM_001194947.1 P231P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:184557508 G>T maps to ENST00000437079 V168V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr3:184947256 G>T maps to NM_001966.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:962668 C>A maps to NM_001347.2 R127R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:3451121 C>A maps to ENST00000511533 P655P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:27010622 C>A maps to ENST00000382009 P591P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:37592328 G>T maps to NM_018302.2 E218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:77065383 C>A maps to ENST00000458189 T71T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:83557888 G>C maps to NM_001037582.2 S219S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:88584222 G>A maps to NM_004407.3 E431E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:141327106 G>T maps to NM_004362.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:159756555 G>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:164247070 G>T maps to NM_000909.4 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:170043323 C>A maps to NM_020870.3 G425*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr4:187628521 G>T maps to ENST00000260147 P820P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr5:32061203 C>A maps to NM_178140.2 P805P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr5:63256859 C>A maps to NM_000524.2 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr5:74066454 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr5:118456724 G>T maps to NM_005509.4 T331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr5:147785872 C>A maps to NM_205836.1 R262R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr5:175824699 C>A maps to NM_007097.2 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:26598854 C>A maps to NM_013375.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:32362550 C>A maps to ENST00000468270 E444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:33236843 C>A maps to NM_022553.4 R165R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:33247612 C>A maps to NM_005452.5 L516L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:33632737 C>A maps to ENST00000374316 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:46830807 G>T maps to NM_015234.4 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:76564976 G>T maps to ENST00000428345 G400G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:84368746 C>A maps to NM_014841.2 G173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:87965891 G>T maps to NM_015021.1 G849*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:109995464 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:111697072 G>T maps to NM_002912.3 R829R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:119226890 C>A maps to NM_014034.2 T100T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:126236517 C>A maps to NM_181782.4 P712P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:131190837 G>T maps to NM_001431.3 P824P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:137245281 C>A maps to NM_001008783.1 I233I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:153347641 C>A maps to NM_012419.4 A52A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr7:2691877 T>C did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr7:99690936 C>A maps to NM_005916.3 G646*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr7:101266283 G>T maps to NM_138403.4 A114A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr7:111517235 C>A maps to ENST00000428084 E532*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr7:124386689 C>A maps to NM_005302.2 T577T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr7:148767850 C>A maps to NM_152411.3 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:6302562 T>C maps to NM_024596.3 A440A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:11704606 C>A maps to NM_147783.2 V249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:17743027 G>T maps to NM_201552.1 T12T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:21839312 G>T maps to ENST00000434536 L352L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:22006173 C>A maps to NM_139278.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:25154119 G>T maps to NM_024940.6 E188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:26509876 C>A maps to NM_001197293.1 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:32611894 G>T maps to NM_013956.3 E241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:33406378 C>A maps to NM_024787.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:42262416 G>T maps to ENST00000417062 L246L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:48775067 C>A maps to NM_006904.6 G1928*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:53092685 G>T maps to NM_014682.2 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:66992698 C>A maps to NM_033105.4 R141R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:91081419 G>T maps to NM_004929.2 R93R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:95390425 C>A maps to NM_012415.2 G833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:121170483 A>G maps to NM_021110.1 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:131104293 C>A maps to NM_018482.2 G833*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:135614407 C>A maps to NM_020863.3 L518L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:139774708 C>A maps to NM_152888.1 G602*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:144809011 C>A maps to NM_198488.3 S873S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr8:145003730 C>A maps to NM_201380.2 E1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr9:32635433 C>A maps to NM_153809.2 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr9:93606497 C>A maps to NM_003177.5 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr9:108424782 C>A maps to NM_005421.2 T2T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr9:111625891 C>A maps to NM_006687.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr9:114174350 C>A maps to NM_001080398.1 S897S. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr9:117848393 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr9:136594897 C>A maps to NM_007101.3 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr9:138845533 C>A maps to NM_016172.2 E109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr9:140109096 G>T maps to NM_001144026.1 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr9:140110217 C>A maps to NM_001144026.1 R466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chrX:37028640 G>T maps to NM_001013736.2 E720*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chrX:39930904 G>T maps to NM_001123385.1 P1012P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chrX:47486666 G>T maps to NM_002621.2 P213P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chrX:56590536 C>A maps to NM_013444.3 A77A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chrX:71359356 C>A maps to NM_001013627.2 S653S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chrX:79932815 G>T maps to NM_153252.4 P1567P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chrX:90691622 C>A maps to NM_080832.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chrX:104464363 C>A maps to NM_031274.3 G172*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chrX:148568477 G>T maps to NM_000202.5 S386S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chrX:152958758 C>A maps to NM_005629.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chrX:153674169 C>A maps to NM_004699.2 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:1269264 G>A maps to NM_152228.1 V660V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:6524735 G>T maps to ENST00000355862 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:6639262 G>T maps to NM_138697.3 L715L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:8931982 G>T maps to NM_001428.2 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:11898626 C>A maps to ENST00000376496 T813T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:14108426 C>A maps to NM_012231.4 P1379P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:16577965 C>A maps to NM_018994.1 V451V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:17555237 C>A maps to NM_013358.2 P257P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:19208357 G>T maps to NM_003748.3 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:19683200 C>A maps to ENST00000375145 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:23688887 C>A maps to NM_001077195.1 T329T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:28282572 C>A maps to NM_014474.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:35370275 G>T maps to NM_001080418.1 R237R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:36056253 C>A maps to NM_178548.3 A308A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:36769509 C>A maps to NM_005119.3 P920P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:39827094 C>A maps to ENST00000361689 R2111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:40435215 C>A maps to NM_001136493.1 S536S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:44137512 C>A maps to NM_014663.2 A567A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:44467232 G>C maps to NM_201649.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:55607306 G>T maps to NM_015306.2 S911*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:65867525 C>A maps to ENST00000371069 P730P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:77620266 C>A maps to NM_005482.2 G285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:78098810 G>T maps to NM_015534.4 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:86954812 C>A maps to NM_001285.3 P439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:91790317 C>A maps to NM_001017975.3 G781*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:92707820 C>A maps to NM_001012425.1 S40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:107599603 G>T maps to NM_018137.2 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:109804970 C>A maps to NM_001408.2 T1483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:109823645 G>T maps to ENST00000409138 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:110168805 G>T maps to ENST00000393689 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:110754165 G>T maps to NM_004978.4 S15S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:116226587 C>T maps to NM_001172412.1 Q324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:118166491 C>A maps to NM_017709.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:118634233 C>A maps to NM_206996.2 E452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:145460263 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:149905377 C>A maps to NM_001145862.1 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:150788882 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:151372077 G>A maps to NM_002796.2 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:155282083 G>T maps to NM_001135821.1 R126R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:156823724 G>A maps to NM_014215.2 T152T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:157653031 C>A maps to NM_052939.3 G605*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:171621193 G>T maps to NM_000261.1 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:179815376 C>A maps to NM_145034.4 T414T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:196438155 C>A maps to NM_198503.2 E143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:197564418 C>A maps to NM_001195215.1 T322T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:203191392 C>A maps to NM_003465.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:203708726 C>A maps to NM_001684.3 P1121P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:203800867 G>T maps to NM_014827.4 V260V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:205497278 C>A maps to NM_212503.2 S349S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:206649578 G>T maps to NM_014002.3 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:207072817 C>A maps to NM_001185156.1 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:207083582 C>A maps to NM_005449.4 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:209800876 C>A maps to NM_000228.2 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:217975147 G>T maps to NM_138796.2 E321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:226074495 G>T maps to NM_020997.2 P344P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:228584678 C>A maps to NM_145214.2 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:236371397 G>T maps to NM_003272.3 L380L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr1:237794768 C>A maps to NM_001035.2 L2161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:888884 C>A maps to NM_015155.1 V211V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:7791173 G>T maps to NM_002216.2 T906T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:15686125 G>T maps to NM_003638.1 S434S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:16996526 G>T maps to NM_001081.3 S1572S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:29820217 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:50531186 C>A maps to NM_001135196.1 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:50857634 C>A maps to NM_020549.4 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:56423962 G>T maps to NM_001142763.1 L20L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:61424014 G>T maps to NM_194298.2 R136R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:61831455 G>T maps to NM_020987.2 P3061P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:61832367 G>T maps to NM_020987.2 P2757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:71148963 G>T maps to ENST00000439900 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:74914206 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:75530048 C>A maps to NM_198597.1 P958P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:75581461 G>T maps to ENST00000423381 T409T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:75609069 C>A maps to ENST00000423381 L121L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:93786405 G>T maps to NM_003972.2 L1711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:99141213 G>T maps to NM_015179.3 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:101439111 C>A maps to NM_020354.3 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:101639927 C>A maps to ENST00000342239 S1420S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:102250026 C>A maps to NM_015490.3 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:102295871 G>T maps to ENST00000442724 E86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:102795319 C>A maps to NM_030971.3 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:116605957 C>A maps to NM_020940.3 S410S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:123673320 G>T maps to NM_001001976.1 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:125622177 C>A maps to NM_198148.2 T155T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:126727724 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:134144952 C>A maps to ENST00000368625 G133G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr10:135024955 C>A maps to ENST00000368572 T1315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:2436250 C>A maps to ENST00000452833 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:3125592 G>T maps to NM_020896.3 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:5718476 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:7507141 G>T maps to NM_198474.3 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:7982609 G>T maps to NM_176821.3 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:16010776 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:18731011 G>T maps to NM_173588.3 R974R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:46637367 C>A maps to NM_173811.3 G140G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:57087968 C>A maps to NM_033396.2 A104A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:58207423 C>A maps to NM_001004733.2 V67V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:60777230 C>A maps to NM_006725.3 S323S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:64004951 C>A maps to NM_003377.3 P157P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DZ-6133-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:64572670 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:67074337 C>A maps to NM_017857.3 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:67352693 C>A maps to NM_000852.3 S106S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:70228204 G>T maps to NM_003626.2 G1188*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:71940154 C>A maps to NM_001567.3 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:72539494 C>A maps to NM_033388.1 R522R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:74988429 C>A maps to NM_004041.3 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:76261156 C>A maps to ENST00000393457 P1313P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:83177860 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:93523837 C>A maps to NM_004268.4 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:93913088 C>A maps to NM_015368.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:102713446 G>T maps to NM_002422.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:111229632 C>A maps to NM_006235.2 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:111747602 C>A maps to ENST00000428306 G154G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:111844943 C>A maps to NM_001037954.2 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:116658335 G>T maps to NM_003904.3 T65T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:123597192 C>A maps to NM_003455.2 G487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:123887120 C>A maps to NM_001004462.1 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:125889558 C>A maps to ENST00000392693 E151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr11:126075617 C>A maps to NM_032795.2 E206*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:306548 C>A maps to NM_003044.3 E357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:6935829 C>A maps to NM_019858.1 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:9095077 C>A maps to NM_002355.2 V215V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:9318697 C>A maps to NM_002864.2 T736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:13761752 G>T maps to NM_000834.3 P598P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:29640713 G>T maps to NM_183378.2 P268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:30790087 C>G maps to NM_006390.3 L841L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:32735298 C>A maps to NM_139241.2 P166P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:48377923 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:50042131 G>T maps to NM_175736.4 S840S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:52818408 C>A maps to ENST00000252245 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:53776798 C>A maps to NM_138473.2 P356P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:53910929 C>A maps to NM_001130059.1 A492A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:57591967 C>A maps to NM_002332.2 P3104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:57602492 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:77202894 C>A maps to NM_015336.2 A131A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:85450907 C>A maps to NM_001079910.1 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:100711660 C>A maps to NM_017988.4 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:109293199 C>A maps to NM_001917.4 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:109926397 C>A maps to NM_183415.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:110009463 C>A maps to NM_052845.3 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:110421191 G>T maps to NM_057169.3 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:113405292 G>T maps to NM_006187.2 A920A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:117486841 G>T maps to ENST00000392545 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:120198742 C>A maps to ENST00000392521 A807A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:121858384 C>A maps to NM_194271.1 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:121972410 C>A maps to ENST00000377071 R256R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:122481864 C>A maps to NM_020993.3 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:124341688 G>T maps to NM_207437.3 S2057S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:124848290 A>G maps to NM_006312.4 N954N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr12:132626914 C>A maps to NM_175066.3 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr13:32869473 C>A maps to NM_023037.2 T2973T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr13:36382372 G>T maps to NM_004734.4 S617S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr13:39420803 C>A maps to NM_207361.4 S2038S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr13:46083902 G>T maps to NM_031431.2 T557T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr13:46288279 C>A maps to NM_152719.1 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr13:52598477 C>A maps to NM_001004127.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr13:60453406 G>T maps to NM_001042517.1 R855R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr13:67801333 C>A maps to NM_203487.2 A413A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr13:110857876 G>T maps to NM_001845.4 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:20665616 C>A maps to NM_001005503.1 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:20845472 C>A maps to NM_007110.4 L2018L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:20925154 G>T maps to NM_080649.1 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:21511180 C>A maps to NM_032572.3 P10P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:21788206 C>A maps to NM_020366.3 T446T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:21864051 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:22102794 C>A maps to NM_001005466.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:23876272 G>T maps to NM_002471.3 R54R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:24545452 C>A maps to NM_006032.2 A340A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:24735665 G>T maps to NM_182836.1 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:32563100 C>A maps to NM_001030055.1 R1076R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:38060761 C>A maps to NM_004496.2 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:39645752 G>T maps to NM_002687.3 G70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:65208191 C>A maps to ENST00000394691 R653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:69341656 G>T maps to NM_001130004.1 P888P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:73733245 C>A maps to ENST00000427855 R1101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:74428156 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:74971851 C>A maps to NM_000428.2 T1401T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:75745696 G>T maps to NM_005252.3 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:75747527 G>T maps to NM_005252.3 E182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:76437971 G>T maps to NM_003239.2 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:77762577 G>T maps to NM_013382.5 R349R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:91744496 G>T maps to NM_001080414.2 P1609P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:92265381 G>T maps to NM_001128596.1 P196P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:100387164 C>A maps to NM_001008707.1 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:102476310 C>A maps to NM_001376.4 R2037R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:102483245 C>A maps to NM_001376.4 A2586A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:105243077 G>T maps to NM_001014432.1 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:105407899 C>A maps to NM_138420.2 G4630*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr14:105611389 C>A maps to NM_002226.3 T987T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:22853741 C>A maps to NM_052903.4 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:31239332 C>A maps to NM_017762.2 T516T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:40756707 G>T maps to NM_014952.3 E672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:42454562 G>T maps to ENST00000348544 L775L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:44864899 G>T maps to NM_025137.3 P2108P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:45353296 C>A maps to NM_003104.5 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:55642895 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:66206282 G>T maps to NM_032445.2 P834P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:72030069 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:72847676 C>A maps to NM_005744.3 T218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:73558702 G>T maps to NM_002499.3 V815V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:78401684 C>A maps to NM_006383.2 E80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:81572096 G>T maps to NM_172217.3 E355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:89867378 C>A maps to NM_002693.2 E677*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:90454050 C>A maps to ENST00000398333 G31G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:90623000 C>A maps to NM_198526.2 A645A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr15:99672830 C>A maps to ENST00000336292 P1421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:277261 G>T maps to NM_201412.1 P45P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:424220 C>A maps to NM_021259.2 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:560729 C>A maps to NM_014700.3 R524R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:1560979 C>A maps to NM_014714.3 E1452*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:20851090 C>T maps to NM_030941.2 A466A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:20975187 C>A maps to NM_017539.1 E3340*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:22162117 G>T maps to NM_173615.3 E1078*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:30664240 C>A maps to NM_024031.2 P107P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:31157240 C>A maps to NM_173502.3 E197*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:31336027 G>T maps to NM_001145808.1 V739V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:31499001 C>A maps to ENST00000431354 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:31500326 C>A maps to ENST00000431354 A469A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:55733514 G>T maps to NM_001043.3 P513P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:56938351 C>A maps to NM_000339.2 R977R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:67575909 C>A maps to NM_001193523.1 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:68598024 C>A maps to NM_133458.2 T445T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:68721619 G>T maps to NM_001793.4 T592T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:81248683 G>T maps to NM_052892.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:81390560 C>A maps to NM_022041.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr16:85111136 C>A maps to NM_014732.2 A227A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:3912911 C>A maps to NM_015113.3 E2907*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:4787698 G>T maps to NM_153827.4 L116L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:4858834 C>A maps to NM_053013.3 P267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:6331820 C>A maps to NM_014336.3 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:7258534 G>T maps to NM_198154.1 L4L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:7416967 C>A maps to NM_000937.4 P1795P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:7535203 C>A maps to NM_001040.3 P241P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:9757855 C>A maps to NM_004246.1 T183T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:10223774 C>A maps to NM_003802.2 A1050A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:16089948 G>C maps to ENST00000395857 S54*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:18022632 C>A maps to ENST00000205890 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:18881937 G>T maps to NM_001039999.2 P347P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:19319205 C>A maps to NM_007148.4 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:19844225 C>A maps to NM_007202.2 E387*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:26851951 C>A maps to NM_003593.2 P185P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:27902846 C>A maps to NM_001085454.1 E588*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:27935881 C>A maps to NM_152345.4 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:28890384 C>A maps to NM_015594.2 S132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:29124389 C>A maps to NM_015986.3 G122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:29280322 C>A maps to ENST00000394782 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:38251276 C>A maps to NM_021724.3 E449*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:38319004 G>A maps to NM_007359.4 W212*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:39723556 C>A maps to NM_000226.3 G614*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:40343228 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:41898360 C>A maps to ENST00000398393 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:42962637 C>A maps to NM_004247.3 T112T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:48447882 C>A maps to NM_016504.2 S35S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:48598535 C>A maps to NM_032133.4 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:48752783 G>T maps to NM_003786.3 T887T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:56424576 C>A maps to NM_003168.1 A86A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:61473154 C>A maps to ENST00000389520 R961R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:67081251 G>T maps to NM_080284.2 P1367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:68129131 C>A maps to NM_018658.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:71433917 C>A maps to NM_001144952.1 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:72736998 C>A maps to NM_001006638.2 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:72921756 C>A maps to NM_178160.2 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:73484905 C>A maps to ENST00000375248 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:73738556 C>A maps to NM_001005619.1 L923L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:73922916 C>A maps to ENST00000389570 G159*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:74772547 C>A maps to NM_024311.2 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:76120700 C>A maps to NM_007267.6 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:76354930 G>T maps to NM_003955.3 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:76501436 C>A maps to ENST00000389840 G1628*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:76970773 G>T maps to NM_005567.3 T124T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:80274600 G>T maps to NM_006137.6 T113T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:80282742 C>A maps to NM_003004.2 E40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr17:80521409 C>A maps to NM_004514.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr18:909618 C>A maps to NM_001117.3 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr18:8088801 C>A maps to NM_001105244.1 T603T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr18:8394566 G>T maps to NM_001105244.1 V1434V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr18:29055883 C>A maps to NM_001944.2 P887P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr18:47799102 C>A maps to ENST00000424334 T625T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr18:72997577 C>A maps to NM_005786.4 A27A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:7267818 G>T maps to NM_000208.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:11231197 G>T maps to NM_000527.4 E714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:11319427 G>T maps to ENST00000319867 S1674S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:12089141 G>T maps to NM_001012753.1 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:13051368 C>A maps to NM_004343.3 P239P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:14939008 C>A maps to NM_017506.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:17039889 C>A maps to ENST00000443236 L1059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:17735691 C>A maps to ENST00000428389 L1469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:17838685 C>A maps to NM_018174.4 P831P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:17983463 G>T maps to NM_000453.2 L112L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:35836518 C>A maps to NM_001771.3 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:36033295 C>A maps to NM_014364.4 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:39328275 C>A maps to ENST00000221419 G525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:40540323 C>A maps to NM_001005851.2 V814V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:42221416 C>A maps to NM_004363.2 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:44130145 G>T maps to NM_145296.1 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:44803800 G>T maps to NM_004234.4 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:46289583 G>T maps to NM_004943.1 A390A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:46308087 C>A maps to NM_030785.3 E359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:46317978 G>A maps to NM_030785.3 Y152Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:46878877 C>A maps to NM_006247.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:49993750 C>A maps to NM_012423.2 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:51379946 C>A maps to NM_005551.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:51729221 C>A maps to NM_001772.3 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:54385885 C>A maps to NM_002739.3 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr19:54600235 C>A maps to NM_130771.3 G100*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:1921067 G>T maps to ENST00000399161 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:10747437 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:25039672 C>A maps to NM_024322.2 T251T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:27527919 G>T maps to NM_032546.3 E245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:28816607 G>T maps to NM_153021.4 G770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:42557055 C>A maps to NM_019063.3 P885P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:60687751 C>A maps to NM_022893.3 T765T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:73519628 C>A maps to NM_001965.3 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:74462239 G>T maps to NM_021196.3 P807P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:74657454 C>A maps to NM_001015055.1 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:75425799 C>A maps to NM_001058.3 V87V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:96920571 C>A maps to NM_017849.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:99154410 C>A maps to NM_001134224.1 R185R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:99193528 G>T maps to NM_001134224.1 L908L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:99232940 C>A maps to ENST00000409347 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:102493543 C>A maps to NM_145686.2 I1043I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:103324924 C>A maps to NM_003048.3 R806R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:103431277 C>A maps to NM_144632.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:108994948 C>A maps to NM_006588.2 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:120734621 C>A maps to NM_002830.2 P919P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:133547658 G>T maps to NM_207363.2 T343T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:136026629 G>T maps to NM_032143.2 R430R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:149847561 C>A maps to NM_004522.1 T585T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:152354181 G>T maps to NM_001164507.1 P8086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:153515783 C>A maps to ENST00000410080 S867S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:158971731 A>G maps to NM_001135098.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:159433805 C>A maps to NM_003628.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:160964189 C>A maps to NM_000888.3 T756T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DZ-6133-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:167056009 G>T maps to ENST00000303354 P1714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:170135898 G>T maps to NM_004525.2 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:170912078 G>T maps to ENST00000442603 A1619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:171687640 C>A maps to NM_000817.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:171854260 C>A maps to ENST00000360843 S680S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:177202241 G>T maps to NM_006554.4 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:179456418 C>A maps to NM_133378.4 G17475*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:179479067 G>T maps to NM_133378.4 P13784P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:179641949 C>A maps to NM_133378.4 T1580T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:200245182 C>A maps to NM_001172509.1 A167A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:201507379 C>A maps to NM_001159.3 P901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:201760065 C>A maps to NM_001136039.2 R227R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:212522507 C>A maps to NM_005235.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:216271198 C>A maps to NM_212482.1 V916V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:217364691 T>A maps to NM_000998.4 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:217526648 G>T maps to NM_000597.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:231077476 T>G maps to NM_080424.2 S194S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:233410272 G>T maps to NM_005199.4 L467L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:233612328 C>A maps to ENST00000373566 R16R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:234399862 C>A maps to NM_018218.2 G999*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:241682386 G>T maps to ENST00000373308 S1200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr2:242607583 G>T maps to ENST00000337606 L369L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:1532595 G>T maps to ENST00000381621 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:2843493 C>A maps to NM_022575.2 P415P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:10632291 C>A maps to NM_000214.2 E353*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:31023544 G>T maps to ENST00000375687 T1010T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:32000157 G>T maps to NM_003098.2 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:33329157 C>A maps to NM_014071.2 A1634A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:33330122 C>A maps to NM_014071.2 G1313*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:39832389 C>A maps to NM_015035.3 T389T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:43139977 C>A maps to NM_006811.2 G143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:45700846 G>T maps to ENST00000360649 G152*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:52601927 C>A maps to NM_003657.2 S346S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr20:62321664 C>A maps to ENST00000482936 R762R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr21:34876756 C>A maps to NM_001136006.1 G935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr21:37741672 C>A maps to ENST00000290384 P670P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DZ-6133-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:17625982 G>T maps to NM_033070.2 T156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:23482574 G>T maps to NM_014433.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:26862216 C>A maps to NM_022081.4 T227T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:28293117 C>A maps to NM_012399.3 T99T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:29521330 C>A maps to NM_032045.4 T186T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:31523435 G>T maps to ENST00000331075 E569*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:32017778 G>T maps to ENST00000422296 P307P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:32019741 G>T maps to NM_014338.3 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:32889176 C>A maps to NM_012179.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:37770572 G>T maps to NM_052906.3 S334S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:37891867 C>A maps to NM_014550.3 L734L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:39078940 C>A maps to NM_020243.4 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:50969635 C>A maps to NM_001014440.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr22:51159807 G>T maps to NM_001080420.1 E1199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:5213858 C>A maps to ENST00000438743 R129R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:8983208 G>T maps to NM_020165.3 P182P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:9695403 C>A maps to NM_001077525.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:38592066 C>A maps to NM_001099404.1 A1932A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:38618265 C>A maps to NM_001099404.1 E1133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:45000690 C>A maps to NM_016598.2 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:45030670 C>A maps to NM_015004.3 R33R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:46622691 C>A maps to NM_003212.3 T173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:47041426 C>A maps to NM_015175.1 R1280R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:47449864 C>A maps to NM_015466.2 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:48603074 C>A maps to NM_000094.3 G2812*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:49049077 C>A maps to NM_018031.3 P67P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:49052492 C>A maps to NM_018031.3 A1076A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:49053483 G>T maps to NM_001009996.1 P455P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:49060194 C>A maps to NM_199069.1 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:49463423 C>G maps to NM_032316.3 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:51690130 C>A maps to NM_015106.2 P1057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:52416386 C>A maps to ENST00000273600 S2619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:52448545 C>A maps to ENST00000454052 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:58154198 C>A maps to NM_001164317.1 R2442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:58625896 C>A maps to NM_138805.2 T110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:63594841 G>T maps to NM_001130003.1 V150V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:63981235 C>A maps to NM_001177387.1 R580R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:66460689 C>A maps to NM_015541.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:69084224 C>A maps to NM_007114.2 A731A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:69998212 G>T maps to ENST00000448226 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:97686161 C>A maps to NM_153182.2 R92R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:122598218 C>A maps to NM_032839.2 S477S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:125850316 C>A maps to ENST00000273450 A521A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:130394225 C>A maps to NM_001102608.1 P2259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:133692537 G>C maps to NM_005630.2 S122S. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:149093237 G>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:170011255 C>A maps to NM_002740.5 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:183454550 C>A maps to NM_018023.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:183858324 C>A maps to NM_003907.2 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:183885815 C>A maps to NM_004423.3 S487S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr3:187447543 G>T maps to NM_001706.4 R217R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:1305801 C>A maps to ENST00000505177 A35A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:2744247 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:2901104 C>A maps to NM_014189.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:2941348 G>T maps to NM_003703.1 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:4322598 C>A maps to NM_145291.3 S618S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:6107448 G>T maps to NM_001099433.1 A125A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:23803442 C>A maps to NM_013261.3 G735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:39839782 G>T maps to NM_001100399.1 R1235R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:47556922 C>A maps to NM_020453.3 R606R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:56225590 G>T maps to NM_024592.3 L100L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:69343242 C>A maps to NM_014058.3 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:70897695 G>T maps to NM_000200.2 G18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:71648836 C>A maps to NM_001037442.2 T308T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:79236787 C>A maps to NM_025074.6 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:79434557 G>T maps to NM_025074.6 S3342S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:79516548 A>G maps to NM_005139.2 E166E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:100003126 C>A maps to NM_000671.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:103504081 G>T maps to NM_003998.3 G299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:114279508 C>A maps to NM_001148.4 P3245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:114824831 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:119951096 C>A maps to NM_133477.2 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:122599617 C>A maps to NM_001154.3 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:129083351 G>T maps to NM_018078.2 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:139966552 C>A maps to NM_012118.2 S407S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:151749354 G>T maps to NM_006726.3 P1716P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr4:155470081 T>C maps to NM_002669.2 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:1219632 G>T maps to NM_001003841.2 L464L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:1479790 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:3599342 C>A maps to NM_024337.3 S94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:34043139 C>A maps to NM_181435.4 G31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:37187662 C>A maps to NM_023073.3 V1311V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:41939606 G>T maps to NM_012176.2 S321S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:50687133 C>A maps to NM_002202.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:52356864 C>A maps to NM_002203.3 R483R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:74655886 C>A maps to NM_000859.2 T845T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:74715184 G>T maps to NM_001130105.1 T348T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:79026621 C>A maps to NM_153610.3 V678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:82815315 C>A maps to NM_004385.4 P397P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DZ-6133-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:90107121 G>T maps to NM_032119.3 G5349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:98233024 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:109110513 C>A maps to NM_002372.2 R408R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-DZ-6133-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:132545896 G>T maps to NM_015082.1 R568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:139947059 G>T maps to NM_080670.2 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:140264174 C>A maps to NM_018904.2 P774P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:140754613 C>A maps to NM_018919.2 R322R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:141007713 C>A maps to NM_003883.3 V244V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:141244926 G>T maps to NM_032420.2 P323P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:147207658 G>T maps to NM_003122.3 T40T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DZ-6133-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:149452928 C>A maps to NM_005211.3 L339L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:149914549 C>A maps to NM_001543.4 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:156378676 G>T maps to NM_138379.2 P175P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:168199888 G>T maps to NM_003062.2 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:176764197 C>A maps to NM_006816.2 T243T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:177688749 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:178373424 C>A maps to NM_182594.2 P33P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:179192535 C>A maps to NM_014757.4 S175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:179305472 C>A maps to NM_198868.2 E540*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr5:180047284 C>A maps to NM_182925.4 T810T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:3155900 C>A maps to NM_001069.2 G79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:28097457 G>T maps to NM_025231.1 T259T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:30627400 C>A maps to NM_003587.4 E619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:30862323 C>A maps to NM_013994.2 L463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:30877828 C>T maps to NM_001517.4 A121A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:30883014 G>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:31696794 C>A maps to NM_013974.1 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:31745373 C>T maps to NM_006295.2 L1264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:32032688 C>A maps to ENST00000375244 S2250S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:32032708 C>A maps to ENST00000375244 E2244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:32714065 C>T maps to NM_020056.4 C221C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:33244221 G>T maps to NM_022551.2 V146V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:43188894 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:44272162 C>A maps to NM_020745.2 V620V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:44390497 C>A maps to NM_001253.2 P452P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:49416552 G>T maps to NM_000255.3 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:52141137 G>T maps to ENST00000419835 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:86176950 G>T maps to NM_002526.2 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:117248653 G>T maps to NM_173560.3 G784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:121605001 G>T maps to ENST00000275159 S476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:135639697 C>A maps to NM_017651.4 E1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:137814776 G>T maps to NM_175747.2 S177S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:155503429 C>A maps to ENST00000456144 P926P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:157527599 G>A maps to ENST00000367148 K1815K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr6:160431774 C>A maps to NM_000876.2 T157T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:7492018 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:21640511 C>A maps to NM_003777.3 P1073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:22196434 C>A maps to ENST00000344041 T390T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:24742393 G>T maps to NM_001127453.1 P414P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:27224694 C>A maps to NM_005523.5 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:28610071 C>A maps to NM_182898.2 T127T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:34118484 G>T maps to NM_133468.3 T365T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:48016344 C>A maps to NM_004507.2 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:56007461 C>A maps to NM_182633.1 T352T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:73790350 C>A maps to NM_003388.4 A540A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:75617586 G>T maps to NM_031925.2 L182L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:77583196 G>T maps to ENST00000427986 G775*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DZ-6133-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:92730688 C>A maps to NM_017654.3 L1574L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:94056351 C>A maps to NM_000089.3 S1046S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:100211240 C>A maps to NM_023948.4 P141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:100350097 C>A maps to ENST00000349350 P790P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:100683336 G>T maps to NM_001040105.1 P2880P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:100684395 G>T maps to NM_001040105.1 P3233P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:107599764 G>T maps to NM_002291.2 A873A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:132990750 C>A maps to NM_021807.3 R198R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:134252935 G>T maps to ENST00000418096 A31A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:138189125 C>A maps to NM_015905.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:138333867 C>A maps to NM_001139456.1 A183A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:142563374 C>A maps to NM_004445.3 A364A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:143016927 C>A maps to NM_000083.2 T87T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:143021535 G>T maps to NM_000083.2 T268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:149467634 C>A maps to NM_207336.1 V15V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr7:150878538 C>A maps to ENST00000422024 A242A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:20004776 C>A maps to NM_001135691.2 E486*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:21927410 C>A maps to ENST00000265800 S138S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:22488016 G>A maps to NM_018688.4 L79L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:25247764 C>A maps to NM_024940.6 P1439P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:25261108 G>T maps to NM_024940.6 T1654T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:32621860 G>T maps to NM_013956.3 E627*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:36693843 C>A maps to NM_001031836.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:37914665 C>A maps to NM_004095.3 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:39862895 G>T maps to NM_194294.2 G253*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:42227365 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:48625273 C>A maps to NM_001080394.1 T676T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:48690357 C>A maps to NM_006904.6 T3976T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:59518594 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:66988990 C>A maps to NM_033105.4 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:68956787 G>T maps to NM_024870.2 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:72111619 C>A maps to NM_000503.4 S578S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:91937823 C>A maps to NM_022351.4 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:95508067 C>A maps to NM_015496.3 G1479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:99440323 C>A maps to NM_020697.2 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:110453070 C>A maps to ENST00000426474 T1363T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:121528422 C>A maps to NM_022045.3 P746P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:127569337 C>A maps to NM_174911.4 P99P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:131949416 C>A maps to NM_001115.2 L461L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:144464047 G>T maps to ENST00000422773 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:144940815 C>A maps to NM_031308.1 T2202T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:144945111 G>T maps to NM_031308.1 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:145065863 C>A maps to NM_001009184.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:145066453 C>A maps to NM_001009184.1 I245I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr8:145624749 C>A maps to NM_013291.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:1056234 G>T maps to NM_181872.4 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:6486846 C>A maps to NM_152896.1 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:8317915 G>T maps to NM_002839.3 A1899A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:19058203 G>T maps to NM_017645.3 S854*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:19521054 C>A maps to NM_020344.2 G525*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:22447687 C>A maps to NM_022160.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:35061056 A>G maps to NM_007126.3 D438D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:35846991 G>T maps to ENST00000360192 T638T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:37432121 C>A maps to NM_012203.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:71835819 G>T maps to NM_004817.3 R120R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:82267551 C>A maps to ENST00000376537 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:96421807 G>T maps to NM_005392.3 E419*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:99799584 G>T maps to NM_001333.2 P115P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:107266629 G>T maps to NM_001004485.1 A29A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:111617632 G>T maps to NM_006686.3 S193*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:111936871 C>A maps to NM_019114.3 E889*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:111962592 C>A maps to NM_019114.3 V656V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:112705260 C>A maps to ENST00000413420 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:113509956 C>A maps to ENST00000189978 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:117068817 C>A maps to NM_032888.2 R1653R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:117120447 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:117680418 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:123210191 G>T maps to NM_018249.4 P1002P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:124929079 C>A maps to NM_198469.2 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:129851285 G>T maps to NM_012098.2 R472R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:130248111 C>A maps to NM_001005374.2 S419S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:130482452 C>A maps to NM_144965.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:131370473 C>A maps to NM_001130438.2 T1470T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:133342135 G>T maps to NM_000050.4 E149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:136215862 C>A maps to NM_000972.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:136341371 G>T maps to NM_017585.3 S183S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:139317559 G>T maps to NM_015160.1 P474P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:139395156 C>A maps to NM_017617.3 T1927T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:140007905 G>T maps to NM_013379.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:140250774 C>A maps to NM_017820.3 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:2343307 C>A maps to NM_145177.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:9000383 C>A maps to NM_205849.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:15315803 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:27998473 C>A maps to NM_001017930.1 V326V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:35993983 C>A maps to NM_152632.3 P889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:41333650 C>A maps to NM_022567.2 T315T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:44703446 C>A maps to NM_022076.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:48651664 C>A maps to NM_002049.3 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:49067892 G>T maps to NM_005183.2 P1394P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:52844125 G>T maps to NM_130775.2 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:54982667 G>T maps to NM_002625.2 R186R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:55650362 C>A maps to NM_198451.3 P73P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:70823633 C>A maps to NM_052957.4 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:71839113 G>T maps to ENST00000373539 R727R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:86071062 G>T maps to NM_053281.3 E571*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:99662149 C>A maps to NM_001184880.1 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:99945149 C>A maps to NM_001129896.2 G244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:107369374 G>T maps to NM_052936.3 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:107929306 C>A maps to ENST00000328300 G1421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:109696176 G>T maps to NM_020769.2 G778*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:118221625 G>T maps to NM_020721.1 P1189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:123197036 C>A maps to NM_001042750.1 T601T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:129147629 G>T maps to ENST00000303743 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:149678293 C>A maps to NM_001177465.1 S635S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:153583299 C>A maps to NM_001110556.1 E1704*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:153589765 C>A maps to NM_001110556.1 G1039G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chrX:154225326 C>A maps to NM_000132.3 V103V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr1:19486772 G>T maps to ENST00000375267 A1803A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr1:42048764 G>T maps to NM_024503.3 T568T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr1:203276559 C>T maps to NM_006763.2 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr12:118506353 T>C maps to NM_019086.5 E465E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr14:55310764 C>T maps to NM_001024024.1 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr16:67424232 C>G maps to NM_016140.2 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr17:10426830 G>A maps to NM_017534.5 I1818I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr17:30632399 C>T maps to NM_138328.2 V274V. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-DZ-6134-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr17:40720855 T>C maps to NM_170607.2 D111D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr19:58596699 G>A maps to NM_001145542.1 A351A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr2:10927528 A>T maps to ENST00000381611 L397L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr5:179751867 G>A maps to NM_005110.2 V208V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr6:34059741 C>T maps to NM_000841.1 W218*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr6:43275461 T>C maps to ENST00000449267 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:63720696 A>G maps to NM_153363.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:100780345 G>C maps to NM_000602.3 V384V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr7:103017285 G>T maps to ENST00000354356 V672V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chr9:116151741 G>A maps to ENST00000277315 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6134-01A-11D-1961-08 chrX:38546885 C>A maps to ENST00000465127 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:1396234 G>T maps to NM_001039211.2 R306R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:10720548 C>A maps to NM_001079843.1 E184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:11740454 G>T maps to ENST00000376669 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:21151676 C>A maps to NM_001198801.1 V1408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:24123377 C>A maps to NM_001008216.1 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:37948725 G>T maps to NM_025079.2 S438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:49056657 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:85491893 G>C maps to NM_018298.9 L302L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:113657106 G>T maps to NM_014813.1 A713A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr1:152552160 G>A maps to NM_032563.1 C84C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr10:5416051 C>A maps to NM_053049.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr10:75277309 C>A maps to NM_152586.3 S958S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr10:81929048 C>A maps to NM_145869.1 G79G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr10:88227263 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr10:116014800 C>A maps to NM_198496.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr11:32449551 G>T maps to NM_024426.4 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr11:61729769 G>T maps to NM_001139443.1 E322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr11:62373389 C>A maps to ENST00000278845 V574V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr11:108124726 G>T maps to NM_000051.3 L695L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr11:123988251 C>A maps to NM_014622.4 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr11:124620610 C>A maps to NM_014312.3 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr12:2694602 G>T maps to NM_199460.2 E801*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr12:46285847 G>T maps to NM_152641.2 G1706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr13:28143268 G>A maps to NM_153371.3 G184G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr13:110830474 C>A maps to NM_001845.4 T854T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr14:45432385 C>A maps to ENST00000361462 T254T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr15:72873182 G>T maps to NM_005744.3 E443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr15:85341270 C>A maps to NM_014630.2 P857P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr16:12618620 C>T maps to NM_001080530.2 N362N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr16:31485236 C>A maps to NM_001042454.2 T88T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr16:48210874 G>A maps to NM_032583.3 R1166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr16:48210904 G>T maps to NM_032583.3 T1156T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr17:30815100 C>T maps to NM_003885.2 L155L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr17:61685280 C>A maps to NM_016360.3 P271P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr17:71361424 C>A maps to NM_001144952.1 L1759L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr17:80887375 G>T maps to NM_005993.4 T997T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr19:1360738 C>A maps to NM_032853.3 P274P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr19:37210705 G>T maps to ENST00000423498 T359T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr19:50393784 C>T maps to NM_172374.1 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr19:52496291 C>A maps to ENST00000354939 P690P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr19:56733045 G>T maps to NM_024303.1 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr2:26204633 C>A maps to NM_002254.6 P51P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr2:48818888 C>A maps to NM_172311.2 S676S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr2:71219104 G>T maps to NM_144582.2 T53T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr2:74128512 T>C maps to NM_001615.3 D25D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr2:74725073 C>A maps to NM_001009812.1 E189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr2:160076201 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr2:166514473 C>A maps to ENST00000409420 R150R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr2:220423049 C>A maps to NM_015311.2 E1120*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr20:5100225 G>T maps to NM_002592.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr22:50659770 G>T maps to NM_020461.3 S1006*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr22:50957132 C>A maps to NM_001185011.1 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr3:19974853 G>T maps to NM_144715.3 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr3:52546616 G>T maps to NM_015136.2 L995L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr3:99514796 C>A maps to ENST00000429802 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr3:164735616 C>A maps to NM_001041.3 G1189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr4:25835076 C>A maps to NM_015187.3 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr4:79321910 G>T maps to NM_025074.6 V1333V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr4:79461753 C>A maps to NM_025074.6 R3839R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr4:84342847 A>G maps to NM_133636.2 F939F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:132197738 C>A maps to NM_005260.3 G303*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:138286864 C>A maps to ENST00000509534 E349*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:140049031 T>C maps to NM_017706.4 H315H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:140856168 C>A maps to NM_002588.2 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:176522538 C>T maps to NM_213647.1 L546L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr5:180432589 C>A maps to NM_197975.2 P373P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr6:70409057 G>T maps to NM_018368.3 T405T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr6:84417535 G>T maps to NM_014841.2 P37P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr6:90428866 G>T maps to NM_014611.1 P2015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr6:148848587 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr7:65547901 G>T maps to NM_000048.3 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr8:38682883 C>A maps to ENST00000379931 R496R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr8:87226833 C>A maps to NM_138817.2 V407V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr9:121930465 G>T maps to NM_014618.2 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr9:139581686 G>A maps to NM_006412.3 S41S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chrX:3238103 G>T maps to NM_015419.3 P1874P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chrX:30578064 G>T maps to NM_025159.2 A136A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chrX:34150359 G>T maps to NM_203408.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chrX:39934343 C>A maps to NM_001123385.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chrX:69720388 C>A maps to ENST00000194900 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chrX:70149808 C>A maps to NM_032803.5 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chrX:79932812 C>A maps to NM_153252.4 R1568R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chrX:129318434 C>A maps to NM_004794.2 P145P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr1:34677971 A>G maps to NM_001134734.1 G562G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr12:57597293 C>A maps to NM_002332.2 C3647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr12:121947831 C>T maps to ENST00000377071 R395R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr13:31821209 A>G maps to NM_194318.3 A107A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr16:354432 G>A maps to NM_003502.3 Y375Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr16:30676957 G>C did not map to a codon.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr2:64199371 T>A maps to NM_016516.2 K129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr2:97216936 G>A maps to NM_212481.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr3:64004273 C>A did not map to a codon.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr5:1488542 A>T maps to NM_024830.3 T210T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr5:131729503 G>A did not map to a codon.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr7:72907198 T>C maps to NM_032408.3 G208G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr9:139908395 G>C maps to ENST00000355090 V1475V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:152279671 C>A maps to NM_002016.1 G2564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:171605340 G>C maps to NM_000261.1 L413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr1:228473854 G>C maps to NM_001098623.1 R3027R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:5717509 C>T maps to NM_006074.4 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:73073119 G>T maps to NM_014786.3 P1510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:76867020 C>T maps to NM_000260.3 H118H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr11:77991911 G>A maps to NM_080491.2 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr16:1718162 C>T maps to NM_020825.3 I1101I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr19:1881549 G>A maps to NM_031213.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr19:49118704 C>T did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:44508524 G>C did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:49190327 G>A maps to NM_000145.3 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:179517426 T>G did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr2:187559028 A>G maps to NM_177454.3 Q43Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr20:21142792 T>A maps to NM_018474.4 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr22:21073054 G>A maps to NM_058004.2 S1666S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:49362338 T>C maps to NM_003363.3 L207L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:138456587 T>C maps to NM_006219.1 V254V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:196214404 G>T maps to NM_152617.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr4:9784111 T>C maps to NM_000798.4 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr5:38954923 A>C maps to ENST00000296782 Y883*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr5:67588177 A>G maps to ENST00000396611 G336G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr7:99753404 G>A maps to NM_018275.3 A428A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr8:144995792 C>T maps to NM_201380.2 A2869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr9:97063237 C>T maps to NM_194320.2 G466G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr9:124074614 A>T did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr1:12304649 T>C maps to NM_015378.2 V141V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr1:62550316 C>T maps to NM_176877.2 P1458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr10:858886 A>G maps to NM_015155.1 T732T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr10:43651226 A>G maps to NM_018590.3 K210K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr11:4929157 C>T maps to NM_001004749.1 L187L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr11:66627367 T>A maps to NM_024036.4 L537*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr11:89537574 G>C maps to NM_020358.2 Y21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:21821860 C>T did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:51219340 T>A maps to NM_020921.3 T1615T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:61434985 T>C maps to NM_002431.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:101198409 C>T maps to NM_003836.5 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr15:77908050 G>T maps to NM_032808.5 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr19:52659396 G>A maps to NM_001102657.1 L513L. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-EV-5903-01A-11D-1589-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:27503081 A>T maps to ENST00000406962 K103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:96789882 G>C maps to NM_001002036.3 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:180810242 A>G maps to NM_020943.2 P780P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:212295692 C>A maps to NM_005235.2 E874*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:220149458 C>A maps to NM_006736.5 S242*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:239988462 A>T maps to NM_006037.3 I981I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr2:242433434 G>C maps to NM_014808.2 V1020V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr20:32376705 G>T maps to ENST00000375200 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr20:40730778 G>A maps to ENST00000373198 N1255N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr5:176639041 T>C maps to NM_022455.4 L1214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr6:83862019 T>A maps to NM_015018.2 P2021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr7:111127298 T>A maps to NM_032549.2 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr8:120114629 A>G maps to NM_006438.3 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr9:36170074 C>T maps to NM_005893.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr9:131755474 G>A did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chrX:48682179 G>A maps to ENST00000444343 R1110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:201166404 C>T maps to NM_001164586.1 Y109Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:207669653 G>C maps to NM_000651.4 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:240255570 C>G maps to ENST00000406993 G197G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr1:241661271 T>G did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr11:2432684 C>T maps to ENST00000452833 A895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr11:95825361 C>T maps to NM_032427.1 Q611Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr12:57440665 G>A maps to NM_005379.2 L174L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr16:20871249 G>A maps to NM_173475.2 L291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr17:4871030 A>C maps to NM_004890.2 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr18:44560192 G>A maps to NM_016427.2 D481D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr19:52327624 T>A maps to NM_002030.3 I208I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr20:36870193 C>T maps to NM_001029864.1 E113E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr5:81549248 G>A did not map to a codon.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr8:29037679 G>A maps to NM_015254.3 R221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-F9-A4JJ-01A-11D-A25F-10 chr9:93375536 C>T maps to NM_017594.3 K191K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr1:10471494 C>A maps to NM_002631.2 G180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr1:35260425 G>T maps to NM_002060.2 T204T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr1:115218254 G>C maps to NM_000036.2 S558S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr1:161722203 C>A maps to NM_007240.1 T208T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr10:106118316 G>T maps to NM_001008723.1 A76A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr10:135011889 C>A maps to ENST00000368572 P652P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr12:29485565 T>C maps to NM_018099.3 L431L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr12:56568457 C>A maps to NM_003075.3 A491A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr13:110822920 C>A maps to NM_001845.4 G1239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr15:74481489 C>A maps to ENST00000449139 V391V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr15:90342656 C>A maps to NM_001150.2 S651S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr17:2241039 G>T did not map to a codon.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr17:78355390 C>G maps to NM_020914.4 G4663G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr17:79496234 C>A maps to NM_001077182.2 G226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr18:33606994 C>T maps to NM_018170.3 A219A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr19:2997884 C>A maps to NM_003260.4 S731S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr19:40408647 G>C maps to NM_003890.2 P1397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr2:37041324 G>T did not map to a codon.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr2:114508133 G>T maps to NM_025181.2 T95T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr2:206659683 C>A maps to NM_201266.1 R900R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr22:33828203 C>A maps to NM_133642.3 G279*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr22:35947760 G>T maps to NM_014310.3 S161S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr3:33557516 C>A maps to ENST00000359576 E1379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr3:52422875 C>T maps to ENST00000273600 L3204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr4:155414 G>T maps to NM_001039127.3 E314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr4:15504479 C>A maps to NM_001080522.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr6:35051231 C>A maps to NM_015245.2 I982I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr6:75798890 C>A did not map to a codon.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr6:110953278 C>A maps to NM_015076.3 R200R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr6:158925120 G>T maps to NM_020245.3 E1476*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr7:90894983 G>T maps to NM_003505.1 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr9:21971119 G>A maps to NM_001195132.1 R80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr9:130586702 G>T maps to NM_001114753.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chrX:44929245 C>A maps to NM_021140.2 A782A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chrX:64721873 C>A maps to NM_001010888.3 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chrX:112054594 C>A maps to NM_001113490.1 S473S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chrX:138832193 G>T maps to NM_173694.4 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr1:13183398 A>G maps to NM_001136561.2 S158S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr1:16332450 G>C maps to NM_178840.2 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr10:71008284 C>A maps to NM_025130.3 T457T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr11:61915971 C>A maps to NM_001040694.1 A743A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr12:14775088 C>A maps to NM_004963.3 P817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr12:75436986 C>A maps to NM_139137.2 A605A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr12:121437342 C>T maps to NM_000545.5 Q561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr14:56107680 C>T maps to NM_001079521.1 Q672*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr15:63356303 G>T maps to ENST00000380364 E272*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr15:83437642 C>A maps to NM_001007122.2 S514S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr16:27509129 G>T maps to NM_001520.3 S726S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:10227378 A>T maps to NM_003802.2 L965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:37368583 C>T maps to NM_198993.3 K399K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:62158135 C>A maps to NM_001433.3 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:73749999 C>G maps to NM_000213.3 G1421G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr18:67992692 C>A maps to NM_004232.3 P263P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr19:5914494 G>T maps to ENST00000394521 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr19:18277095 G>T maps to NM_005027.2 E515*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:141128749 C>A maps to NM_018557.2 E3625*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:171687569 C>T maps to NM_000817.2 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:179419673 A>G maps to NM_133378.4 D26936D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:185801067 A>G maps to NM_194250.1 Q315Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr2:241621873 G>T maps to NM_001102467.1 T127T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G7-6790-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr20:34778269 C>A maps to NM_012156.2 V366V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr20:48713265 T>C maps to NM_199203.2 E261E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr21:11097540 C>A did not map to a codon.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr21:30441793 C>A maps to NM_006585.2 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr22:24034554 C>A maps to ENST00000382833 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr22:24129397 C>A maps to NM_003073.3 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr3:53814150 C>A maps to NM_001128840.1 T1562T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr3:127379598 T>A maps to NM_015720.2 L243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr3:184098192 A>C maps to NM_003741.2 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr5:10377926 C>A maps to NM_005885.2 R13R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr5:138266341 C>T maps to ENST00000355078 R731*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr5:156590093 T>A maps to NM_130899.2 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr6:26021007 C>T maps to NM_003529.2 C97C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr6:37442388 A>G maps to NM_015050.2 L637L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr7:45747950 T>C maps to NM_021116.2 A940A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr7:148947405 C>A maps to NM_012256.3 R61R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr8:33454820 G>T maps to NM_024025.1 L71L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr8:37964559 G>T maps to NM_004674.3 E93*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr8:121237424 A>T maps to NM_021110.1 S612S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr8:121379473 C>A maps to NM_021110.1 P1714P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:17332673 G>A maps to NM_017738.2 K530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:86585224 T>A maps to NM_031262.2 K405*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:94877625 A>T maps to NM_006415.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chrX:2931151 C>A maps to NM_001011719.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chrX:48564667 G>T maps to NM_003173.2 E281*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chrX:129279459 C>A maps to NM_004208.3 G230G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chrX:152937463 A>T maps to NM_001039582.3 G178G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:14108282 C>A maps to NM_012231.4 T1331T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:23403845 G>T maps to NM_001009999.2 T620T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:109792761 T>C maps to NM_001408.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:155912174 G>A maps to NM_181885.2 L225L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:205132070 G>A maps to NM_015375.2 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:226075313 G>A maps to ENST00000419724 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:226076621 C>A maps to NM_020997.2 E49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr10:29776228 C>A did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr10:70775349 G>A maps to NM_015634.3 R348R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr10:101911986 A>G maps to NM_001100626.1 Y316Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr11:1253719 C>A maps to ENST00000447027 P631P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G7-6792-01A-21D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr12:75895545 T>C maps to NM_007043.6 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr12:109692083 C>T maps to NM_001093.3 L2037L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr14:24885904 C>A maps to NM_025081.2 P1650P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr14:57684752 C>T maps to ENST00000340918 K522K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr15:33955871 C>A maps to NM_001036.3 A1851A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr15:77328194 A>G maps to NM_003978.3 T346T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr16:15130100 C>A maps to NM_015027.2 S779*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr17:37817258 G>T maps to NM_006804.3 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr17:76133426 T>G maps to NM_152468.4 V413V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr17:78211364 G>T maps to NM_173626.3 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr19:1469818 G>C maps to NM_005883.2 T2173T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr19:2421952 G>T maps to NM_182973.1 P718P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr19:50103193 C>A maps to NM_020719.1 P1448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr2:9022695 C>A did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr2:12880580 G>T maps to NM_021643.3 S231S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr2:50574024 G>C maps to NM_138735.2 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr2:73198758 C>A maps to NM_144579.2 G227G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr2:102452419 C>A maps to NM_145686.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr2:136570241 G>T maps to NM_002299.2 P664P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr2:241516093 G>T maps to NM_018226.3 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr20:3016488 G>T maps to NM_002836.3 V700V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr20:23548868 G>T maps to NM_080610.2 I73I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr21:43533866 C>A maps to NM_173568.3 V891V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr22:40804934 A>G did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr4:159825695 A>G maps to ENST00000379346 *1138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr4:170043336 A>G maps to NM_020870.3 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr5:176830984 G>A maps to NM_000505.3 G375G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr6:97344646 A>G maps to NM_014165.3 D71D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr7:6183714 G>T did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr7:137773372 G>T maps to NM_005989.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr7:139305248 C>A maps to NM_022740.4 T560T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr7:154681043 C>A maps to NM_130797.2 P789P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr8:19362748 G>T maps to NM_018371.4 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr8:27516953 C>A maps to NM_016240.2 R423R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr8:101719225 C>G did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr9:2039760 A>G maps to NM_003070.3 Q217Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr9:112225704 G>T maps to NM_002829.3 R4R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:6646831 G>T maps to NM_005341.2 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:15986401 C>A maps to NM_006511.1 P13P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:26882105 C>A maps to NM_001006665.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:27179353 C>A maps to NM_032283.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:32653566 C>A maps to NM_175852.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:40533252 C>A maps to NM_001105530.1 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:43788362 G>T maps to NM_005424.2 A1129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:45525905 G>T maps to NM_020883.1 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:51702469 C>A maps to NM_014372.4 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:54717527 C>A maps to NM_145716.2 P171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:100819381 C>A maps to NM_033312.2 S38S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:109241955 C>A maps to NM_018061.2 R319R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:109813134 C>A maps to NM_001408.2 R2466R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:149895853 G>T maps to NM_005850.3 P322P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:151496700 G>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:154042757 G>T maps to NM_207308.2 R849R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:157667659 G>A maps to NM_052939.3 V116V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:179041248 G>T maps to NM_014864.3 V400V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:190067936 C>A maps to NM_199051.1 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:228430953 C>A maps to NM_001098623.1 A1000A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:228560471 C>A maps to NM_001098623.1 S7331S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:228602755 G>T maps to NM_016102.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr1:235840463 C>A maps to NM_000081.2 A3655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:15688932 G>A maps to NM_003638.1 D373D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:16916467 G>T maps to NM_001081.3 I3047I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:27412569 C>A maps to NM_139312.1 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:27687246 G>T maps to NM_001034842.3 A760A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:33211240 C>A maps to ENST00000374956 G358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:48370906 C>A maps to NM_153034.2 P125P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:48390589 G>T maps to NM_002900.2 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:99327794 G>A maps to NM_024954.3 K65K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:102020785 C>A maps to NM_018294.4 G42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:114912174 C>A maps to NM_030756.4 P392P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:115377273 G>T maps to ENST00000369358 T979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:115610050 C>A maps to NM_014881.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:115970643 C>A maps to NM_198795.1 S526S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:116247755 G>T maps to ENST00000277895 P334P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:134999580 C>A maps to ENST00000368572 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr10:135106070 C>A maps to NM_006659.2 A382A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:549919 G>T maps to NM_198075.3 L115L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:981265 C>A maps to ENST00000332231 T224T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:34226097 C>A maps to NM_145804.2 S341S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:45241119 G>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:49186310 C>A maps to NM_004476.1 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:57572165 C>A maps to NM_001085458.1 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:60666361 G>T maps to NM_014502.4 T342T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:62297709 G>T maps to NM_001620.1 P1393P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:62457958 C>A maps to NM_001130702.1 T423T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:63885004 C>A maps to NM_013280.4 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:66191470 C>A maps to NM_178864.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:66612340 C>A maps to NM_005133.2 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:101833305 G>T maps to NM_020802.2 E514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:108380879 C>T maps to NM_015065.2 W1785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:110035108 C>A maps to NM_033390.1 P433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:111631673 C>A maps to NM_181699.2 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:118771646 G>T maps to NM_182557.2 P935P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:120180162 C>A maps to NM_014352.2 S312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:124412653 G>T maps to NM_001005195.1 A299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr11:129246115 G>T maps to NM_003658.4 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr12:1039017 C>A maps to NM_134424.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr12:21629863 C>A maps to NM_032941.2 G310G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr12:43944935 G>T maps to ENST00000389420 R77R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr12:44193305 C>A did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr12:51404511 G>T maps to NM_001174125.1 T29T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr12:54911638 C>A maps to NM_005337.4 R419R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr12:57003661 C>A maps to NM_013449.3 R652R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr12:58120813 G>T maps to NM_001122772.1 S1093S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr12:110784226 C>A maps to NM_170665.3 I1027I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr12:117968801 C>A maps to ENST00000339824 P582P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr12:123351833 C>A maps to NM_024667.2 S229S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr13:39262236 C>A maps to NM_207361.4 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr13:61103197 C>A maps to NM_001146070.1 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr13:77852980 G>T maps to NM_015057.4 S220S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr13:98017411 C>A maps to ENST00000376673 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr13:100920941 G>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr13:110807659 G>T maps to NM_001845.4 S1575S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr13:113770109 C>A maps to NM_000131.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr14:23313869 C>A maps to NM_004995.2 S394S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr14:24801007 C>A maps to NM_139247.3 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr14:54417154 G>T maps to NM_130850.2 T274T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr14:59954534 G>T maps to ENST00000356057 S94S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr14:81743497 G>T maps to NM_033104.2 P719P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr14:91691041 G>T maps to NM_001102368.1 L577L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr14:100551045 C>A maps to NM_016337.2 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr14:102901049 C>A maps to NM_014844.3 P632P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr15:34064241 C>A maps to NM_001036.3 R2980R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr15:59464241 C>A did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr15:65916753 C>A maps to NM_004727.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr15:71300817 G>T maps to NM_017691.3 G424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr15:85487857 G>T maps to NM_004213.3 T575T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr15:89386647 C>A maps to NM_013227.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr15:91419098 G>A maps to NM_002569.2 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:1822946 C>G maps to ENST00000432952 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:2814272 C>A maps to NM_016333.3 P1248P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:3254287 C>A maps to NM_012360.1 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:20376784 G>A maps to NM_174924.1 N398N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:31195323 G>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:57805247 G>T maps to NM_005550.3 T209T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:70572249 G>T maps to NM_012426.4 G284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:89846308 C>A maps to NM_000135.2 T561T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr16:89999918 C>A maps to ENST00000304984 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr17:3851149 C>A did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr17:7133227 C>A maps to NM_004422.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr17:7750677 C>A maps to NM_001080424.1 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr17:7813908 G>T maps to NM_001005271.2 P1977P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr17:28808255 C>A maps to NM_004871.2 R43R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr17:37826278 C>A maps to NM_002686.3 P162P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr17:43246576 C>A maps to NM_144608.1 R88R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr17:77768925 G>T maps to NM_020649.2 L226L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr17:79534499 G>T maps to NM_017921.2 T503T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr18:9533331 G>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr18:19348652 G>T maps to NM_020774.2 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr18:21451553 G>T maps to ENST00000416669 G1645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr18:72103866 C>A maps to NM_001044369.2 E377*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:1207118 G>T maps to NM_000455.4 S69S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:1391116 G>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:4054984 G>T maps to NM_015898.2 A82A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:4171732 C>A maps to NM_032607.1 R385R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:6374897 C>A maps to NM_032306.3 R194R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:8191626 G>T maps to NM_032447.3 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:9964953 G>T maps to NM_058164.2 R425R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:10472831 C>A maps to NM_003331.4 R565R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:12882257 C>A maps to NM_013312.2 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:14674813 G>T maps to ENST00000436007 A111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:14815870 G>T maps to NM_032433.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:17405581 C>A maps to NM_024527.4 G278G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:18870393 G>T maps to NM_001098482.1 G236*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:41837019 C>A maps to NM_000660.4 V370V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:45528981 C>A maps to ENST00000221452 P291P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:45540933 G>T maps to ENST00000221452 P542P. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G7-6793-01A-11D-1961-08. Mapping will be selected arbitrarily.
Reference base specified for sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:52869277 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:55889611 G>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr19:58805578 C>A maps to NM_021089.2 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:3750113 C>A maps to ENST00000403787 P397P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:28635158 G>T maps to NM_005253.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:64796343 C>A maps to ENST00000422803 R736R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:68274378 C>A maps to ENST00000407324 E61*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:68740265 C>A maps to NM_173545.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:84804450 C>A maps to NM_001370.1 P665P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:97024899 G>T maps to NM_015341.3 P442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:112779872 G>T maps to NM_006343.2 R796R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:131102986 G>T maps to NM_033416.1 G79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:131785644 G>T maps to NM_015320.2 L185L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:157186617 C>A maps to NM_006186.3 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:175629095 G>T maps to NM_001039523.2 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:178684946 C>A maps to NM_016953.3 G526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:179425265 A>G maps to NM_133378.4 Y25963Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:182766562 C>A maps to NM_001130445.1 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:203682251 C>A maps to NM_138468.4 V191V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:206992670 G>T maps to ENST00000455934 P592P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:207509299 G>T maps to NM_001102659.1 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:219561850 C>A maps to NM_015690.3 P892P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:225637900 G>T maps to NM_014689.2 L2059L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:239016611 G>T maps to NM_194312.2 E285*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:239261473 G>T maps to NM_015650.3 G486G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr2:242021146 G>T maps to NM_001080437.1 P1324P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr20:1616204 C>A maps to NM_018556.3 V263V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr20:2321110 C>A maps to NM_003245.3 R656R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr20:25260975 C>A maps to NM_002862.3 P389P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr20:39978416 C>A maps to NM_022896.1 L214L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr20:62700773 G>T maps to NM_003195.4 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr21:17138431 C>G maps to ENST00000285681 Y80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr21:32617860 G>T maps to NM_003253.2 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr21:37741556 C>A maps to ENST00000290384 R632R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr21:44839795 G>T maps to NM_173354.3 A354A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr22:20230300 G>T maps to ENST00000425986 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr22:23656897 C>A maps to NM_004327.3 S1241S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr22:31731824 G>T maps to NM_014323.2 R454R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr22:36691726 G>T maps to NM_002473.4 L1103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr22:37171721 C>A maps to ENST00000453009 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr22:40804105 G>T maps to NM_015705.4 L537L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr22:41752026 G>T maps to ENST00000351589 E798*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr22:44369169 G>T maps to NM_015380.4 R205R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr22:46685400 G>T maps to NM_017931.2 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:7494426 C>A maps to NM_181874.2 V436V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:9512465 G>T maps to ENST00000407969 G1035G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:33165979 C>A maps to NM_006371.4 P234P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:48619177 G>T maps to NM_000094.3 P1561P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:49734629 G>T maps to NM_022064.2 V74V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:51297703 C>A maps to NM_004947.4 R768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:51347694 G>T maps to NM_004947.4 R985R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:99514796 C>A maps to ENST00000429802 P685P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:101062696 C>A maps to NM_020654.3 G647*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:112299980 C>A maps to NM_017945.2 T339T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:128126924 C>A maps to NM_021937.3 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:150128648 C>T maps to NM_014779.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:183995974 G>T maps to NM_014693.3 T326T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:185390355 G>T maps to NM_006548.4 P391P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr3:197707306 C>A maps to NM_001136049.2 T220T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr4:1737009 G>T maps to NM_006342.1 T534T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr4:1824003 G>T maps to NM_012318.2 P504P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr4:6864940 G>T maps to NM_014743.2 G944G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr4:25314538 C>A maps to NM_024936.2 P36P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr4:70802173 G>T maps to NM_001890.1 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr4:74007530 G>T maps to NM_032217.3 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr5:14297329 C>A maps to NM_007118.2 T442T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr5:43644744 C>A maps to NM_182977.2 P377P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr5:90106490 C>A maps to NM_032119.3 P5138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr5:95734621 G>T maps to NM_000439.4 R517R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr5:98115542 C>A maps to NM_001012761.2 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr5:102489550 G>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr5:112769660 C>A maps to NM_032028.3 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr5:132362196 C>A maps to ENST00000509437 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr5:176778573 G>T maps to NM_006816.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr5:177669379 G>T maps to ENST00000390654 R486R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:7584148 C>A maps to NM_004415.2 T2218T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:7862550 C>A maps to NM_001718.4 R342R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:24850099 G>T maps to NM_014722.2 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:26225705 C>A maps to NM_003532.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:27833290 G>T maps to NM_003511.2 A53A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:30308096 G>T maps to NM_021253.3 R284R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:31778435 G>T maps to NM_005527.3 P438P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:32137809 G>T maps to NM_032741.4 P204P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:32187468 G>T maps to NM_004557.3 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:33384695 C>G did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:43308640 C>A maps to NM_014345.2 E1128*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:57048574 G>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:84645992 G>T maps to NM_016230.3 E336*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:153043126 C>A maps to NM_025107.2 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:159401968 C>A did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr6:169053645 C>A maps to NM_022138.2 P352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:938775 G>T maps to NM_006869.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:2255916 C>A maps to NM_003550.2 L228L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:6175520 C>A maps to ENST00000404835 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:24324996 C>A maps to NM_000905.3 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:31692268 C>A maps to NM_194300.2 P987P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:33136942 C>A maps to NM_203288.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:36438883 G>T maps to NM_018685.2 L123L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:44607759 G>T maps to NM_019082.2 P482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:48089548 G>T maps to ENST00000430738 G239*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:92761816 C>A maps to NM_152703.2 A1156A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:101559411 C>A maps to ENST00000360264 T27T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:103180838 G>T maps to ENST00000428762 P2245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:141755508 C>A maps to ENST00000475668 R1156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr7:148080930 C>A maps to NM_014141.5 S1222S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr8:2836320 C>A maps to NM_033225.5 V2793V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr8:11615893 C>A maps to NM_002052.3 P413P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr8:22418870 G>T maps to NM_005775.4 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr8:24813294 C>A maps to ENST00000221169 V245V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr8:29207389 C>A maps to NM_001394.5 E136*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr8:56699113 G>T maps to NM_024831.6 P219P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr8:61654401 C>A maps to NM_017780.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr8:62212523 C>A maps to NM_173519.2 P46P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr8:116616109 G>T maps to NM_014112.2 R696R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr8:120831737 C>A maps to NM_003184.3 V49V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr8:125989142 G>T maps to NM_152412.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:27169497 C>A maps to NM_000459.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:36342366 G>T maps to NM_022781.4 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:77343155 C>A maps to NM_017662.4 P1978P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:97563071 C>A maps to NM_001193329.1 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:101797294 G>T did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:108151318 G>T maps to NM_080546.3 S652S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:116152102 C>A maps to ENST00000277315 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:125887893 G>T maps to NM_018387.4 P667P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:128094244 G>T maps to NM_015635.2 L738L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:131367621 C>A maps to NM_001130438.2 P1304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:131392620 G>T maps to NM_001130438.2 S2243S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:132400305 G>T maps to NM_017873.2 P343P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:132671266 C>A maps to NM_015033.2 P399P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:139975258 C>A maps to NM_207309.2 R433R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr9:140997190 G>T maps to ENST00000277549 E1752*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chrX:16864058 A>G maps to NM_001198719.1 F411F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chrX:47086804 G>T maps to NM_001170460.1 E512*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chrX:53616721 C>A maps to ENST00000276009 E1416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chrX:64744930 C>A did not map to a codon.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chrX:153694177 C>A maps to NM_017514.3 P840P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chrX:154013326 C>A maps to NM_002436.3 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:3416194 G>T maps to ENST00000452816 S1049S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:17531775 G>T maps to NM_013358.2 G22*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:22333998 C>A maps to NM_005747.4 S211S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:26665794 G>T maps to NM_001039775.3 T1110T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:43296766 C>A maps to NM_018538.3 T138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:98058808 T>A maps to NM_000110.3 K365*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:150316934 C>A maps to NM_004698.2 R518R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:152193332 C>A maps to NM_001009931.1 G258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:154317123 C>A maps to NM_020452.3 R750R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:155255630 G>T maps to NM_020897.1 P451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:155290237 G>T maps to NM_001135821.1 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:155630356 G>A maps to ENST00000368339 L586L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:157557180 C>A maps to NM_031282.2 P244P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:158369045 C>A maps to NM_001004475.1 E71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:160535365 G>T maps to NM_001184879.1 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:160793510 C>A maps to ENST00000263285 P585P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:180953863 G>T maps to NM_005819.4 R214R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:200867527 C>A maps to NM_018265.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:206647733 G>T maps to NM_014002.3 E50*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:224009057 G>T maps to NM_001031685.2 T13T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr1:243385103 C>A maps to NM_014812.2 V39V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr10:12155006 C>A maps to NM_018706.5 R755R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr10:48428667 C>A maps to NM_004962.2 A406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr10:71129351 C>A maps to ENST00000439900 R318R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr10:71874676 C>A maps to NM_032797.5 P323P. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-G7-6795-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr10:104377121 G>T maps to NM_016169.3 T411T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr10:114925434 C>A maps to NM_030756.4 R499R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr10:124345855 C>A maps to ENST00000368915 S580S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr10:129245793 C>A maps to ENST00000398025 P1895P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:1029526 G>T maps to NM_005961.2 P368P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:1097279 G>T maps to ENST00000441003 L2232L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:4107743 G>T maps to NM_003156.3 T504T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:10647665 C>G maps to NM_001098579.1 R396R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:19955586 C>A maps to ENST00000396087 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:46341821 C>A maps to ENST00000288400 S422S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:59480889 C>A maps to NM_001005324.1 V143V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:62384763 G>T maps to NM_012200.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:64419058 C>A maps to NM_015080.3 T862T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:64785862 C>A maps to NM_001667.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:69972208 G>T maps to NM_018043.5 L335L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:83544656 C>A maps to NM_001142699.1 S574S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:94316699 C>A maps to NM_152431.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:108032023 A>G maps to NM_002519.2 S1263S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:116703527 C>A maps to ENST00000360377 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:116746167 C>A did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:126301308 C>A maps to NM_001161707.1 T567T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:9098016 C>A maps to NM_002355.2 G114*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:56118169 A>T maps to NM_002905.3 R266R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:56360795 G>T maps to NM_001798.3 E2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:56565121 C>A maps to NM_003075.3 A729A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:57918526 C>A maps to NM_052897.3 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:69084483 C>A maps to NM_020401.2 P87P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:109629471 C>A maps to NM_001093.3 T733T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:112884196 C>A maps to ENST00000392596 S44S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:123273348 G>T maps to NM_201435.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:124256169 C>A maps to NM_207437.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr12:124397682 G>T maps to NM_207437.3 R3273R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr13:42729904 G>T maps to NM_178009.2 G198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr13:109475608 C>A maps to NM_015011.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr14:74428010 C>A maps to NM_182476.1 R343R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr14:103418904 G>T maps to NM_006035.3 S1034S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr15:39880742 T>G maps to NM_003246.2 G496G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr15:43021540 G>T maps to NM_138477.2 L809L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr15:44951364 A>T maps to NM_025137.3 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr15:64915130 C>A maps to NM_015042.1 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr15:65236851 G>T maps to NM_182703.3 G357*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr15:72597089 C>A maps to NM_052840.4 G131*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr15:88727468 C>A maps to NM_001012338.1 G104*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:397106 C>A did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:2155891 A>G maps to NM_001009944.2 L2613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:2835801 G>T maps to NM_152891.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:3736137 C>A did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:28893873 C>A maps to NM_173201.3 R143R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:30005400 C>A maps to NM_003609.3 L355L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:30664283 C>A maps to NM_024031.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:31391175 C>A maps to NM_000887.3 S989S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:67184130 G>C maps to NM_033309.2 R86R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:67572649 C>A maps to NM_001193523.1 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:70349980 G>T maps to NM_007242.4 S90S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:72992634 T>C maps to NM_006885.3 E470E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr16:72992637 C>T maps to NM_006885.3 E469E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr17:2898694 C>A maps to NM_015085.4 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr17:4645781 C>A maps to NM_001136046.1 T380T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr17:8416921 C>T maps to ENST00000360416 L893L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr17:15964780 G>T maps to ENST00000395857 R1954R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr17:27959021 C>A maps to NM_033389.2 G1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr17:39471887 C>A maps to NM_031964.1 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr17:54872457 G>T maps to NM_001085430.1 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr17:73753546 C>A maps to NM_001005619.1 R1777R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr18:7888188 C>A maps to NM_001105244.1 T94T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr18:31320332 C>A maps to NM_030632.1 R989R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr18:60612440 C>A maps to NM_194449.2 T1087T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:2408352 G>A did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:18896916 G>T maps to NM_000095.2 P449P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:24310236 A>T maps to NM_203282.2 R479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:35512650 C>A maps to NM_020895.3 R546R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:38774303 G>T maps to NM_021102.3 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:41712374 C>T maps to NM_030622.6 S499S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:42795235 C>A maps to NM_015125.3 A772A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:42840481 C>A maps to ENST00000251268 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:44495783 C>A maps to NM_003445.2 R34R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:45888829 G>T maps to NM_001142502.1 T746T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:48525568 C>A maps to NM_022142.4 T219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:51870813 G>T maps to NM_152353.2 T109T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:57037031 A>G maps to NM_020813.2 Q532Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr19:59082795 C>A did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:21260847 G>A maps to NM_000384.2 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:25505547 C>A maps to NM_175629.1 A70A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:74458395 C>A maps to NM_021196.3 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:74761719 C>A maps to NM_032603.2 L587L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:74906850 C>A maps to NM_004263.3 R610R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:97427612 C>A maps to NM_020184.3 R293R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:102486224 G>T maps to NM_145686.2 E869*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:112705127 C>A maps to NM_006343.2 S247S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:113984804 G>A maps to NM_003466.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:125405381 C>A maps to NM_130773.2 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:136545908 C>A maps to NM_002299.2 P1923P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:137872843 C>A maps to ENST00000272643 A450A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:152522654 G>T maps to NM_001164507.1 P1660P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:159490675 G>T maps to NM_003628.3 A479A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:179598188 G>T maps to NM_133378.4 P4033P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:183699592 G>T maps to NM_001463.3 R321R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:202519625 C>A maps to NM_033066.2 G439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:210640756 C>A maps to NM_032504.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:218686503 G>T maps to NM_022648.4 P1073P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:227924226 C>A maps to ENST00000396625 P759P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:238449467 C>A maps to NM_024101.5 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:13415762 C>A maps to NM_017714.2 G342*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:20491912 A>T maps to NM_020343.3 L1638*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:20493665 C>A maps to NM_020343.3 G1449G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:25188020 C>A maps to NM_001247.2 R122R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:29960924 G>T maps to NM_054112.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:31021204 C>A maps to ENST00000375687 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:32880212 C>A maps to NM_000687.2 G132G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:34261584 C>A maps to NM_021100.4 L386L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G7-6795-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:42680142 C>A maps to ENST00000348077 P212P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:50713912 C>A maps to NM_199427.2 T325T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr20:57415511 C>A maps to NM_016592.2 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr21:31587610 G>T maps to NM_199328.2 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr21:45658358 G>T maps to ENST00000400379 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr22:23656858 T>A maps to NM_004327.3 P1228P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr22:26118389 C>A maps to NM_005160.3 L680L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr22:26688489 C>A maps to NM_021115.4 P71P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr22:30221083 C>A maps to NM_032204.3 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr22:43986109 C>A did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr22:50688065 G>T maps to NM_032019.5 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr3:4836815 C>A maps to ENST00000356617 A2290A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr3:15727626 C>A did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr3:37323487 C>A maps to NM_001172713.1 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr3:48520644 C>A maps to NM_016479.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr3:50396347 C>A maps to NM_007024.4 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr3:52028142 C>A did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr3:112349101 G>T maps to ENST00000447230 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:2648483 C>A maps to ENST00000324666 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:8230106 C>T maps to NM_018986.3 L896L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:109774057 C>A maps to ENST00000333642 T448T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:169317121 C>T maps to NM_001012967.1 R1215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:186382304 C>A maps to NM_152775.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:14507327 C>A maps to NM_007118.2 R2904R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:37381725 C>T maps to NM_018034.2 D38D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:66445361 G>T maps to NM_001164664.1 S1080S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:131607756 C>A maps to NM_003687.3 P276P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:139715602 C>A maps to NM_001945.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:140166267 C>A maps to NM_018900.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:140896561 G>T maps to ENST00000398557 A1225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:150512040 G>T maps to NM_001155.4 A244A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:176895198 C>A maps to ENST00000393565 S55S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:30121874 C>A maps to NM_006778.3 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:32181609 G>T maps to NM_004557.3 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:33170424 C>A maps to NM_006979.2 P296P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:34101198 G>T maps to NM_000841.1 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:37622576 C>A maps to ENST00000297153 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:42986423 C>A maps to NM_057161.2 R263R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:43155044 C>A maps to ENST00000354495 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:73023343 G>T maps to NM_014989.4 E1367*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:109249364 C>A maps to NM_032131.4 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:109322679 C>A maps to NM_014454.1 V119V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:152671890 C>A maps to NM_182961.2 T3865T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr6:159460341 C>A did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:38247284 C>A maps to NM_032016.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:48443360 C>A maps to NM_152701.3 S3985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:48506567 C>T maps to NM_152701.3 N4277N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:100247737 C>A maps to NM_016188.4 R130R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:112108107 C>A maps to NM_001007245.2 R327R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:116776237 C>A maps to ENST00000323984 R272R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:122765635 A>G maps to NM_022444.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr7:129474845 G>T maps to NM_003344.2 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:10466258 C>A maps to NM_178857.5 A1783A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:22865213 C>A maps to NM_001160036.1 R508R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:37732331 C>A maps to NM_001002814.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:59405024 C>A maps to NM_000780.3 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:95565669 C>A maps to NM_015496.3 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:99015916 G>T maps to ENST00000254898 P411P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:106813323 C>A maps to NM_012082.3 T338T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:107718928 T>C maps to NM_001198533.1 L394L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr8:120428850 G>T maps to NM_002514.3 G27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr9:847126 C>A maps to NM_021951.2 P174P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr9:8636764 C>A maps to NM_002839.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr9:35076433 C>A maps to NM_004629.1 T357T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr9:79325590 G>T maps to NM_015225.2 P533P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr9:128206812 C>A maps to NM_001006617.1 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr9:131670997 G>T maps to NM_001127244.1 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr9:132510953 G>T maps to NM_004878.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr9:133759540 C>A maps to NM_007313.2 R641R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr9:135763754 C>A maps to ENST00000372136 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr9:137777154 C>A maps to NM_004108.2 P124P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:601771 C>A maps to NM_000451.3 R195R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:3573398 C>A maps to NM_005044.4 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:9683004 C>A maps to NM_005647.3 R557R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:38546909 G>T maps to ENST00000465127 E277*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:48336438 G>T maps to NM_012280.2 G2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:54280508 C>A did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:70602968 C>A maps to ENST00000449580 P633P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:100276147 C>A maps to NM_001167970.1 V336V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:100629523 C>A maps to NM_000061.2 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:105277619 C>A maps to NM_000354.5 S373S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:107415762 C>A did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chrX:152806950 G>T maps to NM_001001344.2 E115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:6246872 A>T maps to NM_000983.3 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:6586005 C>A maps to NM_024654.4 G673*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:6880293 C>A maps to NM_015215.2 T33T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:10352149 A>G maps to ENST00000377086 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:20107080 G>T maps to NM_181719.4 P57P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:27239996 C>A maps to NM_021969.2 A145A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:27683605 C>A did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:32674957 C>A maps to NM_001099434.1 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:153653693 C>A maps to NM_000906.3 P320P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:157559027 T>C maps to NM_031282.2 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:166845446 C>A maps to NM_053053.3 L8L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:176012403 C>A did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr10:27412569 C>A maps to NM_139312.1 A393A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr10:88717142 G>T maps to NM_024756.2 P52P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr10:95849075 A>G maps to NM_001165979.1 V75V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr10:97388190 G>T maps to NM_002860.3 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:1083145 C>A maps to ENST00000441003 S682S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:9165784 C>A maps to NM_015213.2 G1055*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:10631278 C>A maps to NM_001098579.1 G514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:48185077 C>A maps to NM_002843.3 P1209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:58978546 G>T maps to NM_001039396.1 R598R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:61730353 C>T maps to NM_001139443.1 A516A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:62327540 C>A maps to ENST00000378019 P435P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:62558153 C>A maps to NM_001080501.2 G184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:64517912 C>A maps to NM_005609.2 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:64597528 C>A maps to NM_017525.2 V1127V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:70228263 G>T did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:95825430 T>C maps to NM_032427.1 Q588Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:118485332 C>A maps to NM_015157.2 P40P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr11:128838845 C>A maps to NM_001142685.1 E2074*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:7015022 C>A maps to NM_201650.2 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:21590742 G>T maps to NM_024854.3 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:21962861 G>A maps to NM_005691.2 C1413C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:46246366 C>A maps to NM_152641.2 P1487P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:85450907 C>A maps to NM_001079910.1 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:109186109 C>A maps to NM_018984.3 S615S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:113821908 G>T did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:130184782 C>A maps to NM_133448.2 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr13:45149844 G>T maps to NM_183422.2 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr13:48833063 A>G maps to NM_021999.4 Q232Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr13:110830465 C>A maps to NM_001845.4 S857S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr14:21991799 G>T maps to NM_005407.1 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr14:23887578 G>T maps to NM_000257.2 R1337R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr14:24842405 C>A maps to NM_001136022.1 T526T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr14:102916060 C>A maps to NM_014844.3 P1057P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr14:105677602 C>A maps to NM_001519.2 G618*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr15:34152845 C>T maps to NM_001036.3 R4784*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr15:43574284 C>A did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr15:45427380 C>A maps to NM_175940.1 P129P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr15:81572077 C>A maps to NM_172217.3 P348P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:1417217 C>A maps to ENST00000508903 E641*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:2201893 C>A maps to NM_014353.4 S151S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:15141374 C>A maps to NM_173474.2 G95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:18893555 C>A maps to ENST00000389467 V408V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:27786281 C>A maps to NM_015202.2 P1442P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:31308953 C>A maps to NM_001145808.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:50746032 C>A maps to NM_022162.1 P737P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:67910483 G>A maps to NM_014329.3 K111K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr16:70506466 C>A maps to NM_145059.2 L455L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:3430170 C>A maps to ENST00000381913 S518S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:26857814 C>A maps to NM_003593.2 P293P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:27000490 C>A maps to NM_003170.3 P24P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:32612838 C>A maps to NM_002986.2 S4S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:38182944 G>T maps to NM_014815.3 I588I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:44952528 C>A maps to NM_003396.1 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:45668144 A>G maps to NM_006310.3 V386V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:46608020 C>A maps to NM_002144.3 S82S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:47210425 G>T maps to NM_153446.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:59668145 A>G maps to NM_199290.3 S132S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:72429835 G>T did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr17:79914781 C>A maps to NM_178493.5 T288T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr18:44284578 G>T maps to NM_013305.4 C60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr18:48190783 C>A maps to NM_002747.3 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr18:74154839 C>A maps to ENST00000443185 T57T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr18:76753415 C>A maps to NM_171999.2 P475P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:1993168 G>T maps to NM_017797.3 L178L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:5214455 C>A maps to NM_002850.3 T1510T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:7747429 C>A maps to NM_001042461.1 L97L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:21720535 G>T maps to NM_001001415.2 G561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:32873682 C>A maps to NM_014910.4 P852P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:36128156 G>A maps to NM_024321.3 K411K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:41062002 C>A maps to NM_020971.2 R1700R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:41807609 G>C did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:42192076 G>T maps to NM_006890.3 A6A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:47230770 C>A maps to NM_001039877.1 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:49216661 C>A maps to NM_001130915.1 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:49967136 G>T maps to NM_153329.3 S375S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr19:58945193 T>A maps to NM_003433.3 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:31595112 G>T maps to NM_000379.3 R613R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:85617290 C>A maps to NM_001135023.1 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:86307950 G>T maps to NM_015425.3 P358P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:88367502 C>A maps to NM_198274.3 S40S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:179529596 C>A maps to ENST00000392423 E308*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:219222363 C>T maps to NM_198559.1 Q76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:219509114 A>T maps to NM_001105537.1 T708T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr2:220348802 C>A maps to NM_005876.4 P2206P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr20:3672816 G>T maps to NM_023068.3 R1355R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr20:55021036 C>A maps to NM_020356.3 R181R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr20:61945128 C>A maps to ENST00000326996 A755A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr20:61950485 G>T maps to ENST00000326996 E921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr21:32526660 C>A maps to NM_003253.2 T1025T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr21:47931474 C>A maps to ENST00000318711 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr22:31523392 C>A maps to ENST00000331075 L554L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr22:33673104 G>T maps to NM_133642.3 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr22:33700318 G>T maps to NM_133642.3 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr22:39711371 A>C did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr3:3178957 G>T maps to NM_182916.2 E55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr3:33255597 C>A did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr3:39431017 C>T maps to NM_017875.2 G34G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr3:73453396 C>A maps to NM_015009.1 T356T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr3:129284740 C>A maps to NM_015103.2 A1437A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr3:183823110 C>A maps to NM_182589.2 R221R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr4:40154442 G>T maps to NM_018177.3 T1729T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr4:42119600 C>A maps to NM_207406.3 G513G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr4:68380401 G>T maps to NM_001812.2 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr4:148594114 G>T maps to NM_138364.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr4:186260609 G>T maps to NM_031953.2 T500T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr5:223623 C>A maps to NM_004168.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr5:37725063 C>A maps to NM_018034.2 P542P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr5:140772926 C>T maps to NM_032088.1 Q183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr5:176931622 C>A maps to NM_024872.2 S284S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr6:29692859 C>T maps to NM_001098479.1 T221T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr6:29692865 G>A maps to NM_001098479.1 R223R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr6:43042367 G>T maps to NM_201523.1 R624R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr6:90340446 C>A maps to ENST00000339746 P636P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr7:7546792 C>A did not map to a codon.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr7:28843905 C>A maps to NM_182898.2 R265R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr7:48556447 C>A maps to NM_152701.3 R4590R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr7:63726968 G>T maps to NM_153363.2 G320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr7:129770529 C>A maps to NM_014997.3 R425R. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr8:39496028 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr9:115928425 C>A maps to ENST00000446284 G1223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chrX:3228044 G>T maps to NM_015419.3 P2733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chrX:38019377 C>A maps to NM_006307.4 G283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chrX:53620511 C>A maps to ENST00000276009 G1185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chrX:67272394 G>T maps to NM_002547.2 R788R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:887408 G>T maps to NM_015658.3 P434P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:957786 C>A maps to NM_198576.2 S136S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:1687734 C>A maps to ENST00000344463 G328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:6681625 C>A maps to NM_153812.2 R278R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:10327542 G>T maps to ENST00000377086 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:10473288 C>A maps to NM_002631.2 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:10714268 G>T maps to NM_001079843.1 P615P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:11561091 G>T maps to NM_020780.1 E15*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:12348341 C>A maps to NM_015378.2 S1899S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:16073491 G>T maps to NM_001013641.1 L296L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:16261890 C>A maps to NM_015001.2 T3052T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:16455953 C>A maps to NM_004431.3 E934*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:17318995 G>T maps to NM_022089.2 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:19443748 G>T maps to ENST00000375267 R3597R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:20998554 G>T maps to NM_020816.2 P866P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:21900165 G>T maps to NM_000478.4 E291*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:23238954 G>T maps to ENST00000400191 L905L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:23769116 G>T maps to NM_001143778.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:24384029 G>T maps to ENST00000330966 R1383R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:24841002 C>A maps to NM_013441.2 T47T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:24993365 C>A maps to NM_005839.3 P563P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:26189952 G>T maps to NM_178422.5 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:27106739 G>T maps to NM_006015.4 L2117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:27428593 G>T maps to NM_003047.3 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:27876718 G>T maps to NM_001029882.2 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:28290010 C>T maps to NM_018053.2 C99C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:28661441 G>T maps to NM_017638.2 L196L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:29069106 G>T maps to NM_016258.2 G109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:32098190 G>T maps to NM_012392.3 S177*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:32671843 G>T maps to NM_001160042.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:32671876 C>A maps to NM_001160042.1 P135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:32740363 G>T maps to ENST00000373562 V44V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:32800406 C>A maps to NM_023009.5 E127*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:33954147 C>A maps to NM_145238.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:33960784 C>T maps to NM_145238.3 I947I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:34090660 G>T maps to ENST00000373381 P1790P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:34181885 C>A maps to ENST00000373381 E1033*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:38463362 G>T maps to NM_004468.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:39321579 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:41236481 C>A maps to ENST00000308733 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:41979365 C>A maps to NM_024503.3 V1842V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:42647663 G>T maps to NM_001198850.1 L559L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:43221292 G>T maps to NM_022356.3 R366R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:43396817 G>T maps to NM_006516.2 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:43665075 G>T maps to NM_001195831.1 G482*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:43748484 C>A maps to NM_001164829.1 E105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:43775126 G>T maps to NM_005424.2 A419A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:44476539 G>T maps to NM_201649.2 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:45293784 G>T maps to NM_003738.4 L596L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:45469390 C>A maps to NM_024602.5 L817L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:46093972 G>T maps to NM_021639.4 T460T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:46495223 G>T maps to NM_015112.2 E769*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:46810789 G>T maps to NM_199044.2 G137G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:49056572 C>A maps to NM_032785.3 E346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:54301230 G>T maps to NM_018087.4 T40T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:54671079 C>A maps to NM_016491.3 R215R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:55050458 C>A maps to NM_015547.3 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:55224437 G>T maps to NM_152268.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:55280588 C>A maps to NM_001110533.1 A309A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:57157159 G>T maps to NM_006252.3 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:57411674 G>T maps to NM_000066.2 P308P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:62456018 G>T maps to NM_176877.2 G1284*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:68619273 G>T maps to NM_024911.6 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:68914342 C>A maps to NM_000329.2 E20*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:71418616 G>T maps to NM_198718.1 T410T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:75107047 C>A maps to NM_001002912.4 L137L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:78309082 C>A maps to NM_198549.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:86340385 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:86890023 G>T maps to NM_006536.5 G32*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:94473807 C>A maps to NM_000350.2 G1961*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:95492738 G>T maps to NM_144988.3 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:97839139 C>A maps to NM_000110.3 G679*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:103356018 G>T maps to NM_080629.2 S1460S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:103427451 C>A maps to NM_080629.2 G1058G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:110458277 C>A maps to NM_000757.4 S62*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:110719267 C>A maps to NM_001010898.2 S257S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:115005858 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:115828846 C>A maps to NM_002506.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:116609286 G>T maps to NM_018420.2 L504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:118494624 C>A maps to NM_006784.2 S610S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:118658055 C>A maps to NM_206996.2 T108T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:145533880 C>A maps to NM_003637.3 P509P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:146727485 C>A maps to NM_004284.3 S122S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:149905353 G>T maps to NM_001145862.1 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:150485018 C>A maps to ENST00000369049 L452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:151337048 C>A maps to ENST00000435071 G505G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:152275589 G>T maps to NM_002016.1 T3924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:152281160 G>T maps to NM_002016.1 P2067P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:152283199 G>T maps to NM_002016.1 R1388R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:153603116 G>T maps to ENST00000368698 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:153659195 C>A maps to NM_000906.3 L611L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:153949207 C>A maps to NM_006694.3 V55V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:154300331 C>A maps to NM_020452.3 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:155240741 G>T maps to ENST00000368361 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:156011739 G>T maps to NM_020131.3 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:156126268 C>A maps to NM_022367.3 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:156756542 G>T maps to NM_005973.4 L220L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:158262458 C>A maps to NM_001765.2 S228S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:158389966 G>T maps to NM_001004476.1 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:158687257 G>T maps to ENST00000368146 S232S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:158687901 C>A maps to ENST00000368146 E18*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:159842920 C>A maps to NM_012337.2 E464*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:160124953 C>A maps to NM_144699.3 S109S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:160129299 C>A maps to NM_144699.3 S254S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:160914959 C>A maps to NM_080878.2 T316T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:161011552 G>T maps to NM_007122.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:161514626 G>T maps to NM_000569.6 G183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:166816774 G>T maps to NM_017542.3 E102*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:167368601 G>T maps to NM_002697.3 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:176640165 C>A maps to NM_020318.2 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:176675501 G>T maps to NM_020318.2 G1125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:178427396 G>T maps to ENST00000263528 T979T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:179782981 C>A maps to NM_173509.2 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:186031661 G>T maps to NM_031935.2 V2481V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:186946723 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:192321291 C>A maps to NM_001039152.3 S68S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:196695978 G>T maps to NM_000186.3 V715V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:197108936 C>A maps to NM_018136.4 V662V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:197169317 C>A maps to NM_194314.2 G96*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:200613539 C>A maps to NM_001031725.4 G568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:200967664 C>A maps to NM_017596.2 E642*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:201332476 G>T maps to ENST00000421663 R183R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:202096880 G>T maps to NM_004767.3 G215*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:203676158 G>T maps to NM_001001396.1 T374T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:203678579 C>A maps to NM_001001396.1 S570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:204394797 G>T maps to NM_002646.3 T1553T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:204515998 C>A maps to NM_002393.3 T299T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:206594608 C>A maps to ENST00000414359 S416*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:209803248 G>T maps to NM_000228.2 S322*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:209956835 C>A maps to NM_152485.2 R48R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:210948830 G>T maps to NM_172362.2 S657S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:212530590 C>A maps to NM_006243.3 A397A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:214209129 G>T maps to NM_002763.3 E723*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:214537917 C>A maps to NM_005401.4 G1124G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:214538009 C>A maps to NM_005401.4 E1094*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:216370029 G>T maps to ENST00000366943 P1372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:216498859 C>A maps to ENST00000366943 R310R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:222849560 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:223983834 G>T maps to NM_001031685.2 P802P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:224517802 C>A maps to NM_002533.2 V9V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:224585837 C>A maps to NM_025160.6 G579*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:228468360 C>A maps to NM_001098623.1 G2687G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:229773681 C>A maps to NM_014777.2 R1108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:230840055 C>A maps to NM_000029.3 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:233394124 G>T maps to NM_014801.3 R495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:247608108 C>A maps to NM_004895.4 L999L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:248308493 G>T maps to NM_001004690.1 L15L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:323435 G>T maps to NM_014974.2 P1500P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:373094 G>T maps to NM_014974.2 R1259R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:1313264 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:3161006 C>A maps to NM_002627.3 A492A. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:11505174 G>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:16882893 G>T maps to NM_001081.3 T3272T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:21101818 G>T maps to ENST00000430741 P801P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:33134883 C>A maps to ENST00000375025 R509R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:35858070 C>A maps to NM_145012.4 P333P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:50952121 G>T maps to NM_018245.2 A593A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:52580352 G>T maps to NM_138932.2 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:61043171 C>A maps to ENST00000442566 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:71154790 C>A maps to ENST00000439900 R804R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:72083775 C>A maps to NM_207119.1 L81L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:72179739 C>A maps to NM_004096.4 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:72635218 G>T maps to NM_003901.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:74690313 G>T maps to NM_152635.1 S462S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:75566884 C>A maps to NM_003635.3 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:82272024 G>T maps to NM_030927.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:88451694 C>A maps to NM_001171610.1 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:88705376 G>T maps to NM_024756.2 L78L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:97031498 C>A maps to NM_020992.2 G47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:98806450 G>T maps to NM_003061.2 R605R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:98825843 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:99529478 C>A maps to NM_003015.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:99623814 C>A maps to NM_001010917.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:101478207 G>T maps to NM_078470.4 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:101950725 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:104158503 G>T maps to NM_001077494.1 E334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:112649343 C>A maps to NM_014456.4 T277T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:115337872 C>A maps to NM_004132.3 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:118443397 G>T maps to NM_025015.2 R247R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:118451960 C>A maps to NM_025015.2 A188A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:121652374 G>T maps to NM_007190.2 S27S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:123263455 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:123954553 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:124345757 C>A maps to ENST00000368915 R548R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:129845666 G>T maps to NM_006504.4 P41P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr10:135202522 G>T maps to NM_152911.2 S395S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:1248091 C>A maps to ENST00000447027 L149L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:1901338 G>T maps to ENST00000381758 E154*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:5474964 C>A maps to NM_001004754.2 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:5653608 C>A maps to NM_001003819.3 P370P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:6962823 C>A maps to NM_013250.2 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:7063772 C>A maps to NM_176822.3 T172T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:9608328 C>A maps to NM_003390.3 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:9834102 C>A maps to NM_030962.3 L1377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:10800306 C>A maps to NM_014633.3 S1059S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:16838499 C>A maps to ENST00000448080 S571S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:17757770 C>A maps to NM_001112741.1 G74G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:18741319 G>T maps to NM_173588.3 T213T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:20075624 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:26463597 C>A maps to NM_031418.2 T60T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:34165056 C>A maps to NM_024662.2 S984*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:44129766 G>T maps to NM_000401.3 E202*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:44193163 C>A maps to NM_000401.3 R426R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:45203410 C>A maps to NM_020229.2 R66R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:47362731 G>T maps to ENST00000399249 P618P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:47809813 C>A maps to NM_015231.1 A1222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:49974075 C>A maps to NM_001001955.2 I34I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:56128024 G>T maps to NM_001005205.1 L101L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:56230862 C>A maps to NM_001004743.1 T5T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:57101936 C>A maps to NM_003146.2 S80S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:57427517 C>A maps to NM_006831.2 S190S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:57582965 C>A maps to NM_001085458.1 P934P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:61105435 G>T maps to NM_015533.3 S9S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:61106640 C>A maps to NM_015533.3 A99A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:62065062 C>A maps to NM_206998.1 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:62296407 G>T maps to NM_001620.1 P1827P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:63662659 C>A maps to NM_001039469.2 P28P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:63668086 G>T maps to NM_001039469.2 T275T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:64678637 G>T maps to ENST00000421419 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:65319035 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:65393463 C>A maps to NM_032223.2 P1106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:66062025 G>T maps to NM_153266.3 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:66618301 G>T maps to NM_022172.2 T772T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:67052869 G>T maps to NM_001619.3 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:67412799 C>A maps to NM_080658.1 E162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:71725290 G>T maps to ENST00000393695 T1092T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:86662896 C>A maps to NM_012193.2 G301*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:89135648 G>T maps to NM_016931.3 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:92533738 C>A maps to ENST00000298047 A2520A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:94353309 G>T maps to NM_152431.2 P814P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:95520787 C>A maps to NM_144664.4 T69T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:102564677 G>T maps to NM_022122.2 T384T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:102993714 C>A maps to NM_001080463.1 S549S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:108188242 C>A maps to NM_000051.3 S2114S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:111228520 C>A maps to NM_006235.2 V63V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:111782274 G>T maps to NM_001885.1 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:117789271 G>T maps to ENST00000413475 S100S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:120008505 G>T maps to NM_012101.3 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:120180201 G>T maps to NM_014352.2 V325V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:120328863 C>A maps to NM_015313.2 P767P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:120732720 G>T maps to NM_014619.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:122720813 G>T maps to NM_019604.2 E29*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:129756216 G>T maps to NM_006165.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:133814121 G>T maps to NM_014987.1 T134T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:134226262 C>A maps to NM_138342.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:274931 G>T maps to NM_001170738.1 S949S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:5603934 C>A maps to NM_001102654.1 P198P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:6666437 G>T maps to ENST00000382421 P753P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:6669471 C>A maps to ENST00000382421 V560V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:6692432 G>T maps to ENST00000309577 R1331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:7022148 C>A maps to NM_201650.2 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:9232710 G>T maps to NM_000014.4 R945R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:10321694 G>T maps to NM_002543.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:13208872 C>A maps to NM_020853.1 S142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:14839105 G>T maps to NM_004963.3 T128T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:18699268 G>T maps to NM_004570.4 G1124*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:20774292 C>A maps to NM_000921.3 S496S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:26639108 G>T maps to NM_002223.2 P1913P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:27820106 G>T maps to NM_003622.3 G334*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:31540565 C>A maps to NM_144973.3 G1266*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:31577549 G>T maps to NM_144973.3 T770T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:39709744 C>A maps to ENST00000395670 S1312S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:49334970 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:49937737 G>T maps to NM_012284.1 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:50503241 C>G maps to NM_005276.2 Y330*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:53664547 G>T maps to NM_012291.4 S445S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:56872046 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:57009062 G>T maps to NM_013449.3 P157P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:57871438 C>A maps to ENST00000393797 E258*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:57920109 C>A maps to NM_052897.3 P453P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:83081394 G>T maps to NM_152588.1 L10L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:94613896 C>A maps to NM_005761.1 R554R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:102468172 C>A maps to NM_024057.2 G314*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:105150789 C>A maps to NM_018413.5 R90R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:110290425 C>A maps to NM_016433.3 T188T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:110780223 C>A maps to NM_170665.3 L763L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:112498991 C>A maps to NM_024953.3 L450L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:114839656 C>A maps to NM_000192.3 T72T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:120106075 C>A maps to NM_006253.4 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:120114450 C>A maps to NM_006253.4 I214I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:120586142 C>A maps to NM_006836.1 V1518V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:121764979 C>A maps to NM_016237.4 A453A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:125451741 C>A maps to NM_032656.3 T477T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:129569184 C>A maps to NM_133448.2 V502V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:133768196 C>A maps to NM_001165881.2 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:133779348 C>A maps to NM_001165881.2 P359P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:30829678 G>T maps to NM_032116.3 R133R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:33095587 T>C did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:39422802 C>G maps to NM_207361.4 S2125S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:39452382 C>A maps to NM_207361.4 P2928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:41797442 G>T maps to NM_004294.2 T391T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:43798264 G>T maps to NM_001127615.1 S575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:45978517 C>A maps to NM_001010875.2 G113*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:53035977 C>A maps to NM_001098525.1 P340P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:84453776 C>A maps to NM_052910.1 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:95859035 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:111080929 C>A maps to NM_001846.2 P159P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr13:114782757 C>A maps to ENST00000389544 A394A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:20925312 C>A maps to NM_080649.1 S201S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:21899024 C>A maps to NM_001170629.1 G260*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:31191716 G>T maps to ENST00000311943 V604V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:31374758 C>A maps to NM_001083893.1 G632*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:31598211 C>A maps to NM_015382.2 T1455T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:33290606 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:35548146 G>T maps to NM_173607.3 G141*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:36155750 G>T maps to NM_194301.2 A852A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:36988502 C>A maps to NM_001079668.2 L50L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:39651034 C>A maps to NM_002687.3 R708R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:53138526 C>A maps to NM_014584.1 V140V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:58772825 C>A maps to NM_002892.3 T90T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:59108364 G>T maps to NM_016651.5 S178S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:65210079 C>A maps to ENST00000394691 R1107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:70512972 C>A maps to NM_183002.1 T825T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:72165712 G>T maps to NM_015556.1 S1130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:75416086 C>A maps to ENST00000405431 P96P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:77576242 G>T maps to NM_033426.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:81609691 G>T maps to NM_000369.2 L430L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:81743578 C>A maps to NM_033104.2 T692T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:90651244 C>A maps to NM_022054.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:94582795 G>T maps to ENST00000448882 G101*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:94956067 C>A maps to NM_173850.2 T314T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:96771948 G>T maps to NM_018036.5 P1570P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:99642532 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:105410312 C>A maps to NM_138420.2 S3825S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr14:105420989 G>T maps to NM_138420.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:30064340 C>A maps to NM_003257.3 G80*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:31664324 C>A maps to NM_015995.2 P230P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:31776741 G>T maps to ENST00000382902 S519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:34150114 G>T maps to NM_001036.3 T4714T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:34544585 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:34648788 C>A maps to ENST00000438749 P850P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:34649604 G>T maps to ENST00000438749 L1122L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:35045557 C>A maps to NM_020660.1 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:38988924 G>C maps to NM_207444.2 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:40093560 C>A maps to NM_007223.1 V440V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:41794207 G>T maps to NM_002220.1 E273*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:41815127 G>T maps to NM_015540.2 S859S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:42003279 C>A maps to ENST00000219905 T939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:42840436 G>T maps to NM_153260.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:43818788 C>A maps to ENST00000382031 V1944V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:44046025 G>T maps to NM_005313.4 G58*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:45433259 C>A maps to NM_175940.1 T519T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:45434179 C>A maps to NM_175940.1 P564P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:45803335 C>A maps to NM_013309.4 E180*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:49088257 C>A maps to NM_001194998.1 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:50578246 G>T maps to NM_002041.4 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:50836824 C>A maps to ENST00000456636 V69V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:51024808 G>T maps to NM_032802.3 P335P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:55965830 G>T maps to NM_173814.4 P530P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:56388239 G>T maps to NM_022841.5 P562P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:58465345 G>T maps to NM_020980.3 V106V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:59348030 C>A maps to ENST00000434298 T386T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:62359940 G>T maps to NM_207322.2 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:64005068 G>T maps to ENST00000261887 R1497R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:64792314 G>T maps to NM_015042.1 E233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:64967929 G>T maps to NM_015042.1 S959S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:65297260 C>A maps to NM_139242.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:65678968 C>A maps to NM_020962.1 T957T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:65983243 C>A maps to ENST00000443035 E1230*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:66207936 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:70347483 G>T maps to NM_005078.2 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:72548829 G>T maps to NM_020214.2 P367P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:74967447 C>A maps to NM_025083.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:75137509 C>A maps to NM_005697.3 E302*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:85147250 C>A maps to NM_181877.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:85401013 G>T maps to NM_020778.4 L1217L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:86807664 G>T maps to NM_152336.2 T375T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:89071002 C>A maps to NM_017996.3 V377V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:90767096 C>A maps to NM_198925.2 A357A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:91475003 G>T maps to ENST00000394272 P113P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:91811775 C>A maps to NM_014848.4 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:424855 G>T maps to NM_021259.2 T492T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:775275 G>T maps to NM_001031737.2 T151T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:2003990 G>T maps to NM_005061.2 T54T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:2030178 C>A maps to NM_172168.1 R140R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:2313278 G>T maps to NM_080594.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:2506576 C>A maps to NM_001761.2 T639T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:2511751 C>T maps to NM_025108.2 L204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:4432424 C>A maps to NM_138440.2 S516*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:4504908 C>A maps to NM_005147.4 T479T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:10525247 C>A maps to NM_024997.2 T257T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:14742418 C>A maps to NM_016561.2 S146S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:16357001 C>A maps to ENST00000263012 T489T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:19490785 C>A maps to NM_001105248.1 R735R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:19661778 C>A maps to NM_020314.5 R791R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:21008629 G>T maps to NM_017539.1 P2192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:23391764 G>T maps to ENST00000307331 L567L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:23546254 G>T maps to NM_001083614.1 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:27856299 G>T maps to NM_001109763.1 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:28502881 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:28841981 C>A maps to NM_148414.1 R361R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:28948646 C>A maps to NM_001178098.1 S418S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:29871907 G>T maps to NM_006319.3 T136T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:30536239 G>T maps to NM_024671.3 G407G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:31046333 C>A maps to NM_004604.3 S117S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:31508262 C>A maps to NM_022744.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:46615793 G>T maps to NM_024745.4 S622S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:49433165 G>T maps to NM_144602.2 G259*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:55690641 C>A maps to NM_001043.3 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:56468325 C>A maps to NM_007006.2 L193L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:57292454 G>T maps to NM_015993.2 T117T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:67645004 G>T maps to NM_006565.3 V90V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:67778299 C>A maps to NM_020850.1 S153S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:68391117 C>A maps to NM_019023.2 T690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:68721436 G>T maps to NM_001793.4 T531T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:69419347 G>T maps to NM_005652.3 R99R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:69905721 G>T maps to NM_007014.3 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:77369704 G>T maps to NM_199355.2 R603R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:81942155 G>T maps to NM_002661.2 E565*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:84888431 C>A maps to NM_031476.3 R236R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:85010700 C>A maps to NM_001145548.1 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:87367823 G>T maps to NM_024735.3 P355P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:89349904 G>T maps to NM_013275.4 P1015P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:89717998 G>C maps to NM_001083314.1 G21G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:90038222 C>A maps to NM_145039.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr16:90095729 C>A maps to NM_001214.3 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:3779555 G>T maps to ENST00000381771 P357P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:4458244 C>A maps to NM_001105538.1 E69*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:4498561 C>A maps to NM_001114974.1 S310*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:4645215 G>T maps to NM_001136046.1 L278L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:4845903 C>A maps to NM_015528.1 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:4846567 G>T maps to NM_015528.1 G189*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:6329108 C>A maps to NM_014336.3 E276*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:6599180 G>T maps to NM_177550.3 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:7496410 G>T maps to NM_004860.3 P473P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:7689916 C>A maps to NM_020877.2 S2126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:7691281 C>A maps to NM_020877.2 P2236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:7802755 G>T maps to NM_001005271.2 V872V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:8171849 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:8218442 G>T maps to NM_173728.3 E370*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:8285480 G>T maps to NM_000987.3 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:17053489 C>A maps to NM_015134.2 S436S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:17719258 G>T maps to NM_001005291.2 P796P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:18063319 C>A maps to ENST00000205890 T3125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:18181214 C>A maps to NM_004618.3 L867L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:27024636 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:30326018 C>A maps to NM_015355.2 L739L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:32598754 C>A maps to ENST00000378569 P88P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:34881145 C>A maps to NM_001163735.1 V109V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:34945742 C>A maps to NM_024835.3 R666R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:35937532 G>T maps to NM_007247.4 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:36478172 C>A maps to NM_032351.3 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:37565539 G>T maps to NM_004774.3 T978T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:38126783 G>T maps to NM_178171.4 E148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:40034382 G>T maps to ENST00000401700 T864T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:40622190 C>A maps to NM_001130020.1 T126T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:41342781 G>T maps to NM_005899.3 L284L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:42426627 G>T maps to NM_002087.2 L32L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:43246662 G>T maps to NM_144608.1 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:46675134 C>A maps to NM_018952.4 P126P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:48541199 C>A maps to ENST00000427954 T381T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:48916888 C>A maps to NM_175575.5 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:56355332 C>T maps to ENST00000340482 L385L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:56383004 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:57272143 C>A maps to NM_018304.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:57643046 C>A maps to NM_024612.4 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:58329764 C>A maps to NM_032582.3 P371P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:62498175 C>A maps to NM_004396.3 G390*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:65014303 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:65941612 G>T maps to ENST00000321892 V2389V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:66864262 G>T maps to NM_007168.2 S1570*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:67023203 G>T maps to NM_080283.3 R655R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:71381993 G>T maps to NM_001144952.1 R1521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:71391492 G>T maps to NM_001144952.1 S1131S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:73008930 C>A maps to NM_001545.1 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:73127316 C>A maps to NM_014595.1 P78P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:73263948 G>T maps to NM_020679.2 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:73567808 C>A maps to NM_001031803.1 S746S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:73914073 G>T maps to ENST00000389570 S761*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:74080606 C>A maps to NM_001145297.2 P640P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:74942474 C>A maps to NM_198955.1 P631P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:76089200 C>A maps to NM_001142640.1 P1383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:76528584 G>T maps to ENST00000389840 T1031T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:77709356 C>A maps to NM_178543.3 P305P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:78073420 C>A maps to NM_017950.2 S1092S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:78360676 C>A maps to NM_020914.4 R5019R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:80014727 C>A maps to NM_212492.1 R463R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:3168949 G>T maps to NM_003803.3 R402R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:5396283 C>A maps to NM_012307.2 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:9208695 G>T maps to NM_015208.3 G116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:9275634 C>A maps to NM_015208.3 A1959A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:12344172 C>A maps to NM_006796.2 A579A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:12802023 G>T maps to NM_002828.2 R329R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:19997765 G>T maps to NM_172241.2 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:20577606 G>T maps to ENST00000360790 G685*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:29046520 G>T maps to NM_001944.2 T480T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:29205724 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:43243771 C>A maps to NM_007163.3 P458P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:55992304 C>A maps to NM_001144967.1 P197P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:60242515 G>T maps to NM_017742.4 G1068*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:61654193 C>A maps to NM_198833.1 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:72176135 C>A maps to NM_018235.2 A143A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:72345350 C>A maps to NM_017757.2 S792S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:72347537 G>T maps to NM_017757.2 V1521V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr18:72997763 G>T maps to NM_005786.4 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:603579 G>T maps to NM_001194.3 V223V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:1790768 C>A maps to NM_138813.2 E789*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:1800298 G>T maps to NM_138813.2 L434L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:3433549 C>A maps to ENST00000269778 S223S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:4013244 G>T maps to NM_015897.2 G118*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:4504541 C>A maps to NM_001080400.1 E1335*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:4685730 C>A maps to ENST00000357909 S725S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:5144813 G>T maps to NM_015015.2 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:6147518 G>T maps to NM_030924.3 G44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:6429773 C>A maps to NM_173637.3 L195L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:6468351 C>A maps to NM_024898.2 E562*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:7964534 C>A maps to NM_025061.3 L376L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:9267948 G>T maps to NM_020933.4 S56S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:9271571 C>A maps to NM_020933.4 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:9639088 G>T maps to NM_024106.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:10091808 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:10624853 C>A maps to NM_001166215.1 P278P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:11447928 G>T maps to NM_004283.3 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:12767861 C>A maps to NM_000528.3 L476L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:12786362 G>T maps to NM_032332.3 V275V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:12826466 C>A maps to NM_001136196.1 E138*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:12984831 C>A maps to NM_014975.2 L1287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:13920032 G>T maps to NM_023072.2 L337L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:14160112 C>A maps to NM_004843.2 S463S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:14938213 C>A maps to NM_017506.1 V280V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:15061197 G>T maps to NM_005071.1 R502R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:16611909 C>A maps to NM_032207.2 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:16799118 C>A maps to NM_024074.1 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:17039016 C>A maps to ENST00000443236 E1115*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:17728643 C>A maps to ENST00000428389 A1563A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:18100535 C>A maps to ENST00000222249 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:18182934 G>T maps to NM_005535.1 A336A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:18331047 G>T maps to NM_000923.3 R264R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:18426869 G>T maps to NM_012321.3 P3P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:35530553 C>A maps to NM_001037.4 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:36125171 G>T maps to NM_024321.3 L344L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:36207198 G>T maps to NM_014383.1 G397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:36340179 C>A maps to NM_004646.3 V266V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:37880273 C>A maps to NM_032453.1 P441P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:38779781 C>A maps to NM_021102.3 P114P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:39437176 C>A maps to NM_148169.1 L173L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:39899188 G>T maps to NM_003407.2 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:41622212 G>T maps to NM_000774.3 L40L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:42510820 G>T maps to NM_002088.3 A671A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:42736239 C>A maps to NM_019884.2 A449A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:44159599 C>A maps to NM_002659.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:47569672 C>A maps to NM_015168.1 A1284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:47763855 G>T maps to NM_015603.2 L74L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:47969036 G>T maps to NM_015063.2 A208A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:49259526 G>T maps to NM_019113.2 G12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:49344548 G>T maps to NM_020904.2 R588R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:49377479 C>A maps to NM_014330.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:50097990 G>C maps to NM_020719.1 S133S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:50549107 C>A maps to NM_015428.1 R470R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:50939935 C>A maps to NM_004533.3 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:51015788 C>A maps to NM_001114598.1 G161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:51870726 G>T maps to NM_152353.2 P138P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:51983647 G>T maps to NM_001080405.1 L99L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:52001512 G>T maps to NM_053003.2 A388A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:53208452 C>A maps to NM_001161500.1 E619*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:53792952 C>A maps to NM_033341.3 A225A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:55176599 C>A maps to ENST00000391733 P242P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:55708066 C>A maps to NM_002842.3 E694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:55785951 G>T maps to NM_012267.4 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:57724180 G>T maps to NM_003417.4 V572V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:3504620 G>T maps to NM_018269.3 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:17955657 C>T maps to NM_001130009.1 Q398*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:20205928 C>A maps to NM_002381.4 V122V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:21229323 G>T maps to NM_000384.2 T3472T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:24255777 C>A maps to NM_025203.2 A619A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:26532907 C>A maps to NM_001145168.1 V1048V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:27424245 C>A maps to NM_021095.2 V540V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:32734958 G>T maps to NM_016252.3 E3379*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:36775699 G>T maps to NM_016441.2 V989V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:37129878 C>A maps to NM_003162.2 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:43819492 C>A maps to ENST00000330266 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:47702162 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:50149369 G>T maps to ENST00000404971 G1452G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:55201873 G>T maps to NM_020532.4 T1129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:55254580 C>A maps to NM_020532.4 S218S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:55522973 C>A maps to ENST00000436346 A1770A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:58468359 G>T maps to NM_001114636.1 S30*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:65480880 G>T maps to NM_001005386.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:69034471 C>A maps to NM_001007231.2 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:70444039 G>T maps to NM_022173.2 P187P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:70444050 G>T maps to NM_022173.2 R184R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:72359526 C>A maps to NM_019885.2 V456V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:74326594 G>T maps to ENST00000409262 E1061*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:74594855 C>A maps to NM_004082.4 V717V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:96860715 G>T maps to NM_020151.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:96944034 G>T maps to NM_014014.3 S1850S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:98173405 C>A maps to NM_025190.3 G355*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:98392350 G>T maps to NM_015348.1 T1425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:105859427 G>T maps to NM_007227.3 A371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:111691167 C>A maps to NM_001142807.1 T336T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:112779157 G>T maps to NM_006343.2 V783V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:113498458 G>T maps to NM_152515.3 R650R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:114691914 C>A maps to NM_005721.3 T164T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:120003278 C>A maps to NM_182915.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:125521620 G>T maps to NM_130773.2 A809A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:128066228 C>A maps to NM_006609.3 T522T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:128081817 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:128263013 G>T maps to NM_017969.2 P155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:128477665 C>A maps to NM_018383.4 G645*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:150069635 G>T maps to NM_177964.3 T153T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:158116046 G>T maps to NM_014568.1 G485*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:165946776 G>T maps to NM_006922.3 S1962S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:166003530 C>A maps to NM_006922.3 A463A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:167273492 C>A maps to NM_002976.2 V1046V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:168107850 C>A maps to NM_152381.5 R3317R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:170094636 G>T maps to NM_004525.2 T1490T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:172411330 C>A maps to NM_024843.3 T285T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:175432714 C>A maps to NM_003387.4 G406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:178705093 C>A maps to NM_016953.3 E462*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:178981006 C>A maps to ENST00000456670 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:179412854 G>T maps to NM_133378.4 T28598T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:179500755 C>A maps to NM_133378.4 G11280*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:189904253 C>A maps to NM_000393.3 P1223P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:191864364 G>T maps to NM_007315.3 T176T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:201337658 C>A maps to ENST00000409151 R397R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:202593786 G>T maps to NM_020919.3 P900P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:204304743 C>A maps to ENST00000374493 G1109*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:204304942 G>T maps to ENST00000374493 P1042P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:207620006 C>A maps to NM_001039845.1 V212V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:208633267 C>A maps to NM_003468.3 E66*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:209169615 C>A maps to NM_015040.3 S505S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:212989614 C>A maps to NM_005235.2 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:216271174 G>T maps to NM_212482.1 T924T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:216960883 C>A maps to NM_138390.3 P66P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:219507119 C>A maps to NM_001105537.1 R1373R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:219679710 C>A maps to NM_000784.3 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:219878723 G>T maps to NM_194302.2 L1215L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:220343907 C>A maps to NM_005876.4 T1690T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:220355313 C>A maps to NM_005876.4 L3035L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:225265906 C>A maps to NM_001122779.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:227967564 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:231253298 C>A maps to NM_138402.4 T270T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:231741582 G>C maps to NM_030926.4 A154A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:233323080 C>A maps to NM_001631.3 S382S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:234396950 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:234638543 C>A maps to NM_019093.2 R258R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:234858708 C>A maps to NM_024080.4 A353A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:238275795 C>A maps to NM_004369.3 V1678V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:239988450 C>A maps to NM_006037.3 S985S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:2843725 C>A maps to NM_022575.2 T449T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:3102330 G>T maps to NM_014948.2 P318P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:3557534 C>A maps to NM_139321.2 P748P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:5159571 C>A maps to NM_003818.2 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:6064801 G>T maps to NM_017671.4 R535R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:17602102 C>A maps to ENST00000377813 T1138T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:17716323 G>T maps to NM_001159495.1 L54L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:33342582 G>T maps to NM_014071.2 T539T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:40743922 C>A maps to ENST00000373198 T1027T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:44511477 C>A maps to NM_080603.4 R83R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:44670099 C>A maps to NM_001134771.1 A352A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:45022173 G>T maps to ENST00000439931 T62T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G7-6797-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:45133253 C>A maps to ENST00000331711 G55*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:50234091 C>A maps to NM_006045.1 G784G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:52198378 G>T maps to NM_006526.2 S329S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:55982811 C>A maps to NM_017495.4 A210A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:62221441 C>A maps to NM_012384.3 *531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr20:62221479 C>A maps to NM_012384.3 E519*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:30432924 C>A maps to NM_006585.2 L502L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:32554797 G>T maps to NM_003253.2 R943R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:33368175 C>A maps to NM_014586.1 P467P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:37833864 G>T maps to NM_001146077.1 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:39087225 G>T maps to NM_002240.2 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:42729108 C>A maps to ENST00000398652 P270P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:43547922 C>A maps to NM_173568.3 P1352P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:43716366 G>T maps to NM_004915.3 S634S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:45717567 C>A maps to NM_000383.2 A532A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:45786794 G>T maps to ENST00000397932 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:45861594 G>T maps to ENST00000397932 S1519S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:46698061 C>A maps to NM_133635.4 E221*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:47616132 G>T maps to NM_002340.5 A573A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr21:47836623 G>T maps to NM_006031.5 A2264A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:19119013 C>A maps to NM_053006.4 L34L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:19864708 G>T maps to NM_006440.3 P498P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:19964965 G>T maps to NM_001670.2 A614A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:22048924 G>T maps to NM_148175.2 E414*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:23237840 G>T maps to ENST00000410090 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:24472173 G>T maps to NM_012295.3 E897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:24916396 C>A maps to NM_016327.2 A278A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:29085137 G>T maps to NM_001005735.1 P552P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:29684659 G>T maps to NM_013986.3 G293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:29694820 C>A maps to NM_013986.3 R511R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:30051665 G>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:30134371 C>A maps to NM_019103.2 L110L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:30639825 G>T maps to NM_002309.3 A141A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:30891408 C>A maps to NM_174977.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:31829875 C>A maps to NM_004147.3 L341L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:35802565 G>T maps to NM_006739.3 L148L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:36055549 C>A maps to NM_030641.3 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:37260972 G>T maps to NM_013416.3 E44*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:37627310 G>T maps to NM_002872.3 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:37688717 C>A maps to NM_013385.3 R26R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:38201665 G>T maps to NM_005318.3 E39*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:40708963 C>A maps to ENST00000454349 A1561A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:40754972 G>T maps to ENST00000428371 R623R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:41075458 G>T maps to NM_005297.3 G4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:41076968 G>T maps to NM_005297.3 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:41360109 G>T maps to NM_014248.3 G73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:41670660 C>A maps to NM_002883.2 V61V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:42033663 C>A maps to NM_001469.3 S214S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:42071197 G>T maps to ENST00000402458 A46A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:50893762 C>A maps to ENST00000337034 E1492*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:50899973 C>A maps to ENST00000337034 T949T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:50925340 G>T maps to NM_017584.5 V5V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:50960659 C>A maps to NM_001185011.1 R405R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:50969655 G>T maps to NM_001014440.3 R128R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:3085379 G>T maps to NM_175607.1 G935*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:4735184 G>T maps to ENST00000356617 S1343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:8590489 C>A maps to NM_014583.2 P208P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:10107579 G>T maps to NM_033084.3 G768*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:10391805 G>T maps to NM_001001331.2 T798T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:12623387 C>A maps to NM_014160.3 P350P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:12966228 C>A maps to ENST00000429247 G528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:25622194 C>A maps to NM_000965.3 A256A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:35833976 G>T maps to ENST00000458225 P713P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:39228827 C>A maps to NM_194293.2 L703L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:42576538 G>T maps to NM_004624.3 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:45996859 C>A maps to NM_024513.2 P1275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:47891409 G>T maps to NM_138615.2 E1129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:47956412 C>A maps to ENST00000426837 T648T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:47960331 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:48624941 G>T maps to NM_000094.3 S968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:48668740 T>C did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:49728651 C>A maps to NM_022064.2 T18T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:49885583 G>T maps to NM_005879.2 R50R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:50251673 C>A maps to NM_006841.4 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:50326034 C>A maps to ENST00000336089 S543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:50379016 C>T maps to NM_015896.2 W412*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:50415492 C>A maps to ENST00000435965 L475L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:52012069 G>T maps to ENST00000463937 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:52021192 C>A maps to ENST00000463937 R331R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:52257665 C>A maps to ENST00000494383 L375L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:52438502 C>A maps to NM_004656.2 E406*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:52549486 C>A maps to NM_015136.2 R1305R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:52557717 C>A maps to NM_015136.2 A2447A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:52802365 G>T maps to NM_003157.4 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:53894169 G>T maps to NM_018725.3 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:53907075 C>A maps to NM_022899.4 G382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:55514883 G>T maps to NM_003392.3 S23S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:58517531 C>A maps to NM_003500.3 R197R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:69928455 G>T maps to ENST00000448226 V92V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:81640208 G>T maps to ENST00000264326 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:86010670 C>A maps to NM_153184.3 R275R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:87322539 G>T maps to NM_001122757.1 S83S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:96706413 G>T maps to NM_001080448.2 G231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:112992180 C>A maps to ENST00000273395 S409S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:118935162 G>T maps to NM_212543.1 R276R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:119306533 C>A maps to NM_001125.2 R295R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:120122158 A>G maps to NM_007085.4 N208N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:121097632 C>A maps to NM_014980.2 A773A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:126736707 C>A maps to NM_032242.3 P1211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:128878015 G>T maps to ENST00000418265 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:130394225 C>A maps to NM_001102608.1 P2259P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:133166186 C>A maps to NM_003571.2 A172A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:137822312 C>A maps to NM_173543.2 T167T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:140675512 C>A maps to NM_001104647.1 P62P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:150421459 C>A maps to NM_152394.3 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:152554236 C>A maps to NM_002563.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:154146429 G>T maps to NM_001038705.1 P325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:157081191 C>A maps to NM_001167912.1 G566*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:157841738 C>A maps to NM_016625.2 S93S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:172062008 C>A maps to NM_022763.3 T737T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:182870221 G>T maps to NM_014398.3 R277R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:183524802 G>T maps to NM_018023.4 E1312*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:183663664 C>A maps to NM_005688.2 S1159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:183894832 C>A maps to ENST00000411763 R18R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:184070598 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:184105798 C>A maps to NM_003741.2 T844T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:185327064 C>A maps to ENST00000427465 R292R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:185375142 C>A maps to NM_006548.4 V439V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:186953789 G>T maps to NM_139125.3 P623P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:193855916 C>A maps to NM_005524.2 P246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:194362951 C>A maps to NM_018385.2 G608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr3:195481189 G>T maps to NM_018406.5 S5074S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:155779 C>A maps to NM_001039127.3 S435S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:654314 G>T maps to NM_000283.3 L509L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:884383 C>A maps to NM_005255.2 G339G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:884404 C>A maps to NM_005255.2 L332L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:1330647 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:3444466 G>T maps to ENST00000511533 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:3768716 G>T maps to NM_000683.3 L128L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:8621184 C>A maps to NM_001014447.2 P600P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:9982310 C>A maps to NM_020041.2 E196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:15839737 G>T maps to NM_001775.2 V203V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:25831766 G>T maps to NM_015187.3 T370T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:26487515 G>T maps to NM_000730.2 T123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:39306527 C>A maps to ENST00000381897 V673V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:46973115 G>T maps to NM_000809.2 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:48143406 C>A maps to NM_003215.2 A500A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:55963933 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:57860655 C>A maps to NM_000938.1 P110P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:62845291 G>T maps to ENST00000506720 A939A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:69188585 G>T maps to NM_001031732.2 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:72332249 C>A maps to NM_001098484.2 T529T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:73169666 G>T maps to NM_014243.1 T797T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:74964352 G>T maps to NM_002089.3 P91P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:80976348 C>A maps to NM_001145794.1 G170G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:83411360 C>A maps to NM_001080506.1 G132*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:83840025 C>A maps to NM_024672.4 T887T. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:84230618 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:85634364 C>A maps to NM_014991.4 T2663T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:85752722 C>A maps to NM_014991.4 A204A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:88029463 G>T maps to NM_001166693.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:103556061 C>A maps to NM_005908.3 R766R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:110791017 G>T maps to NM_198506.2 P326P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:111470877 C>A maps to NM_001977.3 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:114257054 C>A maps to NM_001148.4 R1145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:114294592 C>A maps to NM_001148.4 T3949T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:122301607 C>A maps to NM_198179.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:126238366 C>A maps to NM_024582.4 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:126238618 G>T maps to NM_024582.4 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:144361255 G>T maps to NM_207123.2 G436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:156632003 G>T maps to NM_001130684.1 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:158142909 C>A maps to NM_000826.3 P60P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:159533317 G>T maps to ENST00000440678 P218P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:177608987 C>A maps to NM_005429.2 S266S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:184186176 G>T maps to ENST00000448232 G652G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:184240783 C>A maps to NM_001111319.1 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:185550458 G>T maps to NM_032991.2 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:185940981 C>A maps to NM_001029887.1 R157R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:186318446 C>A maps to NM_181726.2 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:186324680 G>T maps to NM_018359.3 T430T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:187004969 C>A maps to NM_003265.2 T710T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:187510246 C>A maps to ENST00000260147 T4425T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr4:187630249 C>A maps to ENST00000260147 T244T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:1441600 G>T maps to NM_001044.4 A97A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:5462002 G>T maps to NM_015325.1 S852S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:10286608 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:14316674 C>A maps to NM_007118.2 P518P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:36035934 G>T maps to NM_174914.3 P479P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:54416332 C>A maps to NM_001170402.1 G421*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:54557236 G>T maps to NM_019030.2 R1307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:56219611 C>A maps to ENST00000381226 T372T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:59064086 C>A maps to NM_001197218.1 T83T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:66480334 G>T maps to NM_005582.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:71499571 C>A maps to NM_005909.3 R2399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:75581668 C>A maps to NM_014979.1 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:78423713 C>A maps to NM_001713.2 A315A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:79374037 G>T maps to NM_003248.4 V751V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:94830476 C>A maps to NM_014639.3 A1237A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:98223925 C>A maps to NM_001270.2 G788*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:102360934 G>T maps to NM_000919.3 S862S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:112770362 G>T maps to NM_032028.3 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:118183838 C>A maps to NM_173666.2 L224L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:122682410 G>T maps to NM_153223.3 S921S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:128441047 C>A maps to NM_016048.2 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:131325794 C>A maps to NM_001009185.1 E150*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:133686004 C>A maps to NM_001113575.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:136476303 G>T maps to NM_004598.3 T104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:137013251 G>T maps to NM_017415.2 T206T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:140262845 G>T maps to NM_018904.2 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:140502470 G>T maps to NM_018938.2 T297T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:140625727 G>T maps to NM_018935.2 L194L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:140966761 C>A maps to ENST00000398557 L49L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:141008782 C>A maps to NM_003883.3 T189T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:141052171 G>T maps to NM_022481.5 V444V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:141693893 C>A maps to NM_030964.3 L283L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:141980317 G>T maps to NM_001144935.1 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:145849105 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:148586577 C>A maps to NM_014945.2 A152A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:149361234 C>A maps to NM_000112.3 S693S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:149513155 G>T maps to NM_002609.3 T309T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:149644564 C>A maps to NM_015981.3 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:150632815 G>T maps to NM_000405.4 L13L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:150647056 C>A maps to NM_001167607.1 P139P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:156734782 C>A maps to ENST00000442283 G270G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:158135116 C>A maps to NM_024007.3 S538S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:158139282 G>T maps to NM_024007.3 P476P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:162918134 C>A maps to NM_001142556.1 R715R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:173317860 G>T maps to NM_030627.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:176332408 G>T maps to ENST00000377219 P679P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:176764372 G>T maps to NM_006816.2 G222G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:176795209 C>A maps to ENST00000398128 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:176798537 G>T maps to ENST00000398128 L483L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:176863230 C>A maps to NM_002082.3 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:176966052 C>A maps to ENST00000442143 L102L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:178419051 C>A maps to NM_000843.3 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:178996333 G>T maps to NM_025158.3 E246*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr5:179193450 C>A maps to NM_014757.4 P480P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:2623938 C>A maps to NM_152554.2 G40*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:2959509 C>A maps to ENST00000316782 L52L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:3324168 C>A maps to ENST00000436008 A327A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:7904883 G>T maps to NM_030810.3 A112A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:10902995 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:10956423 C>A maps to NM_001040274.2 A704A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:13486930 C>A maps to NM_018988.2 V64V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:17292028 G>T maps to NM_001143942.1 P130P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:17764481 G>T maps to NM_022113.4 S1759S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:26104396 G>T maps to NM_003542.3 T74T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:26107961 G>T maps to NM_005323.3 T120T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:28403731 G>T maps to NM_001012455.1 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:29395265 C>A maps to NM_013937.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:29797393 G>A maps to ENST00000376828 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:30862335 G>T maps to NM_013994.2 G467G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:32063763 G>T maps to ENST00000375244 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:32150738 C>A maps to ENST00000375070 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:32805575 G>T maps to ENST00000452392 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:32819973 G>T maps to NM_000593.5 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:33284177 C>A maps to NM_001145338.1 G172G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:33391260 G>T maps to NM_006772.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:37247376 C>A maps to NM_017772.2 S137S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:38882975 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:39304324 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:39869758 G>T maps to ENST00000398904 G1051G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:41196715 G>T maps to NM_198153.2 G110*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:41704664 C>A maps to NM_002630.3 G364G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:42203945 C>A maps to NM_033502.2 G1021G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:42976838 C>A maps to NM_006245.2 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:42978204 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:42985613 C>A maps to NM_057161.2 R119R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:43153859 G>T maps to ENST00000354495 V306V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:43155044 C>A maps to ENST00000354495 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:43267634 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:43323484 G>T maps to NM_014345.2 P529P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:43417678 C>A maps to NM_033450.2 I1415I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:44392245 G>T maps to NM_001253.2 E499*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:46623589 C>A maps to NM_004277.3 P39P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:46658324 C>A maps to NM_001010870.2 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:54219371 C>A maps to NM_014464.3 T396T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:56391226 G>T maps to ENST00000361203 R5810R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:56438653 G>T maps to ENST00000361203 S4142S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:70970386 G>T maps to NM_001851.4 T474T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:79918263 C>A maps to NM_004242.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:80723017 C>A maps to NM_003318.4 R307R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:87928402 G>T maps to NM_015021.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:89793470 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:100056667 G>T maps to ENST00000359773 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:108234611 G>T maps to NM_007214.4 R158R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:109285498 G>T maps to NM_032131.4 G757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:116757271 C>A maps to NM_013352.2 P547P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:117113841 G>T maps to NM_148963.2 S748S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:118588217 C>A maps to NM_001029858.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:123369837 C>A maps to NM_001010852.2 T212T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:128718723 G>T maps to ENST00000368210 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:132891546 G>T maps to NM_175067.1 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:132891894 C>A maps to NM_175067.1 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:135510955 C>A maps to NM_001130173.1 R81R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:135679269 C>A maps to NM_017651.4 T1055T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:139167796 C>A maps to NM_001195037.2 R296R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:149730785 C>A maps to NM_015093.4 T671T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:155450510 G>T maps to ENST00000456144 G52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:159682293 C>A maps to NM_032532.2 T1749T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:167343198 C>A maps to ENST00000428859 P266P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:169648760 G>T maps to NM_003247.2 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:5330830 G>T maps to NM_153247.2 L126L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:6036999 C>A maps to NM_000535.5 E254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:17889972 G>T maps to ENST00000417048 G402G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:21598466 C>A maps to NM_003777.3 S181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:29927726 G>T maps to NM_001080529.1 A381A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:33136942 C>A maps to NM_203288.1 T115T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:41739735 G>T maps to NM_002192.2 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:45016627 C>A maps to NM_033054.2 L46L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:45750241 C>A maps to NM_021116.2 G1016G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:56156627 G>T maps to NM_006213.3 R3R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:73112160 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:77267950 G>T maps to NM_002835.3 A728A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:86541471 C>A maps to NM_001142749.2 V695V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:98589794 C>A maps to ENST00000359863 P3268P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:99662134 C>A maps to NM_145914.2 T439T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:99704098 C>A maps to ENST00000429084 R374R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:100205371 C>A maps to NM_002593.3 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:100231073 G>T maps to NM_003227.3 T193T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:100684572 G>T maps to NM_001040105.1 T3292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:100880739 G>T maps to NM_014343.2 T41T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:102087039 G>T maps to NM_032831.2 T102T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:102109393 G>T maps to NM_152892.1 R371R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:103155710 G>T maps to ENST00000428762 P2680P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:105658433 G>T maps to NM_152750.4 L523L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:111430661 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:115889178 C>A maps to NM_015641.2 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:117180330 G>T maps to NM_000492.3 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:129045003 C>A maps to NM_015328.3 T364T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:133314870 C>A maps to NM_021807.3 T497T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:134873211 G>T maps to NM_014149.3 T618T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:135269596 G>T maps to NM_015135.2 E354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:137308228 C>A maps to NM_004717.2 A292A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:140225583 C>A maps to NM_015689.3 V838V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:141708396 G>T maps to ENST00000475668 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:142724093 C>A maps to NM_001001658.1 T42T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:143175357 C>A maps to NM_176883.2 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:149481028 C>A maps to NM_198455.2 A837A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:150037212 G>T maps to NM_002889.3 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:158727107 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:158734704 G>T maps to NM_018051.4 A956A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:2815227 G>T maps to NM_033225.5 T3268T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:21984790 C>A maps to NM_005144.4 S388S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:22548165 C>A maps to NM_004430.2 T328T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:22900711 G>T maps to NM_003842.4 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:24209519 T>C maps to NM_014265.4 H733H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:25364992 C>A maps to ENST00000434814 P938P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:26240663 C>G maps to NM_004331.2 V6V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:37729418 C>A maps to NM_001002814.2 S967S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:38775548 C>A maps to NM_021623.1 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:39780986 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:41554204 C>A maps to ENST00000415018 P908P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:42294976 C>A maps to NM_006749.3 S351S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:48800125 G>T maps to NM_006904.6 A1517A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:54870844 C>A maps to NM_170587.2 R332R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:56435873 C>G maps to NM_052898.1 A347A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:59409541 G>T maps to NM_000780.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:65528596 G>T maps to NM_004820.3 P167P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:67577660 G>T maps to NM_025054.4 P511P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:68007602 G>T maps to ENST00000389042 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:70585517 G>T maps to NM_030958.2 T711T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:72129212 C>A maps to NM_000503.4 G396*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:94935499 C>A maps to NM_001161778.1 R464R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:105261713 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:105441929 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:106815087 C>A maps to NM_012082.3 S926S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:120599283 C>A maps to NM_006209.3 T465T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:124267151 G>T maps to NM_007222.3 P345P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:126011785 C>A maps to NM_003129.3 R47R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:127569208 C>A maps to NM_174911.4 V142V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:139890115 C>A maps to NM_152888.1 E179*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:141745381 C>T maps to NM_005607.4 R688R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:142367837 G>T maps to NM_005293.2 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:144124642 C>A maps to NM_173687.2 P50P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:144459603 G>T maps to ENST00000422773 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr8:144809761 G>T maps to NM_198488.3 G623G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:5534917 G>T maps to NM_025239.3 E77*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:5921983 C>A maps to NM_001017969.2 G1338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:22451756 C>A maps to NM_022160.2 P454P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:32485173 G>T maps to NM_014314.3 L493L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:34622445 C>A maps to NM_001017363.1 E316*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:35609498 G>T maps to NM_006285.2 L547L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:72347099 G>T maps to NM_001099666.1 S199S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:72356751 G>T maps to NM_001099666.1 T93T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:72521021 C>A maps to NM_001010940.1 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:77354734 C>A maps to NM_017662.4 P1797P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:79323693 G>T maps to NM_015225.2 R1166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:79324369 G>T maps to NM_015225.2 S940S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:97382751 G>T maps to NM_001127628.1 T64T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:101706442 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:101984129 G>T maps to NM_033087.3 S16*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:103064573 C>A maps to NM_017746.3 G897*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:104190795 C>A maps to NM_000035.3 G112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:104309133 C>A maps to NM_019592.5 A260A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:114134733 G>T maps to NM_001080398.1 T1679T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:114178593 G>T maps to NM_001080398.1 T752T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:114246955 G>T maps to NM_001080398.1 R24R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:115928363 C>A maps to ENST00000446284 L1243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:116925048 C>A maps to NM_032888.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:117819657 G>T maps to NM_002160.2 P1451P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:122000987 C>A maps to NM_014618.2 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:123330631 G>T maps to NM_018249.4 P54P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:125315672 C>A maps to NM_001004457.1 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:128067395 C>A maps to NM_015635.2 R362R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:128069690 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:130487068 C>A maps to NM_144965.1 A384A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:131072154 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:131373991 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:131670330 C>A maps to NM_001127244.1 T296T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:131811715 C>A maps to NM_032809.2 A159A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:133952711 G>T maps to ENST00000355048 P1256P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:135786056 C>A maps to NM_000368.4 L388L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:135940072 C>A maps to NM_001807.3 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:136412217 C>A maps to ENST00000393061 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:136501831 G>T maps to NM_000787.3 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:139289302 C>A maps to NM_003086.2 E167*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:139925206 G>T maps to NM_004479.3 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:140007905 G>T maps to NM_013379.2 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:140083647 G>T maps to NM_003731.2 L61L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr9:140948314 G>T maps to ENST00000277549 V1276V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:5827146 C>A maps to ENST00000381093 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:7894126 C>A maps to NM_001142389.1 G12*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:8591692 C>A maps to NM_000216.2 E92*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:10096191 C>A maps to NM_015691.3 S757S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:11174683 C>A maps to NM_013427.2 V624V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:11316354 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:16142471 G>T maps to NM_005314.2 T132T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:27999048 C>A maps to NM_001017930.1 E135*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:30709267 C>A maps to ENST00000378948 T122T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:31279099 G>T maps to ENST00000357033 P3086P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:32613911 C>A maps to ENST00000357033 G522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:37027235 C>A maps to NM_001013736.2 P251P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:39923699 G>T maps to NM_001123385.1 R1131R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:46952306 G>T maps to NM_152869.2 L287L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:47106786 C>A maps to NM_004651.3 S878S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:47272038 C>A maps to NM_003446.3 P189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:48434009 C>A maps to NM_006743.3 T55T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:48826569 G>T maps to NM_004979.4 R37R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:48849858 G>T maps to NM_020137.3 A146A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:51486757 C>A maps to NM_018094.4 P12P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:52847213 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:53607875 G>T maps to ENST00000276009 A1877A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:53629560 C>A maps to ENST00000276009 E979*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:54037717 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:54960265 C>A maps to NM_002625.2 R448R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:64138933 G>T maps to NM_018684.2 P183P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:69890364 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:70347859 C>A maps to ENST00000333646 T1033T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:70347871 G>T maps to ENST00000333646 T1037T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:70596810 G>T maps to ENST00000423759 G182*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:70823663 C>A maps to NM_052957.4 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:71521713 G>T maps to NM_001144885.1 I173I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:79932778 C>A maps to NM_153252.4 E1580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:79945542 G>T maps to NM_153252.4 A1217A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:83723734 G>T maps to NM_144657.4 S332S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:100880266 C>A maps to NM_016607.3 R100R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:105011204 G>T maps to NM_017416.1 G538*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:105152717 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:107424136 G>T maps to NM_033641.2 P671P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:108719036 G>T maps to ENST00000218006 S43S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:108926381 C>A maps to NM_022977.2 G112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:109697625 C>A maps to NM_020769.2 R1261R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:117731502 A>T maps to ENST00000276204 A791A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:117785971 G>T maps to ENST00000276204 G1543*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:118222929 C>A maps to NM_020721.1 G755*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:119496038 C>A maps to NM_001142447.2 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:128722214 G>T maps to NM_000276.3 L772L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:128946749 C>A maps to NM_016032.3 G241*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:134156206 G>T maps to NM_001078173.1 R95R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:135618271 C>A maps to NM_016267.3 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:151123241 C>A maps to NM_004961.3 S484S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:152612319 C>A maps to ENST00000095634 A115A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:153129786 G>T maps to NM_000425.3 T1104T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:153215062 G>T maps to ENST00000369984 T2048T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:153608344 C>A maps to NM_000117.2 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chrX:154090067 G>T maps to NM_000132.3 T2216T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G7-7501-01A-11D-2201-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:153736637 A>G maps to ENST00000428986 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:207085118 G>C maps to NM_005449.4 P222P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr1:207105816 C>G maps to NM_002644.3 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr11:65829381 C>A maps to NM_006842.2 P630P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr12:122616845 C>T maps to NM_014938.3 F336F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr13:35733739 A>C maps to ENST00000400445 T1144T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr16:87377236 G>C maps to NM_024735.3 Y208*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr19:58490169 A>G maps to NM_025027.3 C626C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr2:179567315 C>A maps to NM_133378.4 E8856*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr21:15579136 T>C maps to NM_198996.2 S36S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr4:41748006 T>G maps to NM_003924.3 A254A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr4:89575197 G>T maps to NM_014606.1 E231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr4:170658831 G>T maps to NM_017867.2 R239R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr6:39159333 G>A maps to NM_003740.3 Q278*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:7845602 A>C maps to ENST00000377532 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:28477259 G>A maps to NM_001164721.1 N91N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:32646098 T>C maps to NM_175852.3 A51A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr12:49433379 C>G maps to NM_003482.3 L2689L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr16:50104087 G>A did not map to a codon.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr17:46058012 C>T maps to NM_176096.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr19:19789580 G>C maps to NM_033204.2 L59L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr2:175215407 T>C maps to NM_004882.3 K219K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr2:219556969 C>G maps to NM_015690.3 L623L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr2:233350796 G>A maps to NM_004826.2 D189D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr20:5903929 T>C maps to NM_001819.2 S380S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr20:57599036 G>A maps to NM_030773.3 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:52022537 A>C did not map to a codon.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:52554290 C>A maps to NM_015136.2 C1828*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:108110609 G>A maps to NM_014981.1 S1829S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:122128620 C>T maps to NM_014367.3 N136N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr3:142238532 G>A maps to NM_001184.3 L1454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr4:54362297 G>A maps to NM_001126328.1 G414G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr5:156899850 C>T maps to NM_001099287.1 P428P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:8102675 C>A maps to NM_004280.4 E27*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:32945265 T>C maps to ENST00000395289 A416A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:139563746 T>C maps to ENST00000358430 A657A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr6:170117954 C>A maps to NM_018288.3 E125*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr7:19738031 C>T maps to NM_001002926.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr7:27211694 C>T maps to NM_018951.3 E352E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:27736339 A>G maps to NM_006990.2 P395P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:42744041 T>A maps to NM_001198850.1 R116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr1:113244308 C>G maps to NM_175744.4 R145R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr11:62301414 C>T maps to NM_001620.1 T158T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr11:94341804 C>T maps to NM_152431.2 D632D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr12:95867963 T>G maps to NM_006838.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr12:109889449 G>T maps to NM_031954.3 R298R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr16:3860636 G>A maps to NM_004380.2 I314I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr17:73487467 G>T maps to ENST00000375248 E446*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr20:47587773 C>G maps to NM_006420.2 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr3:98600600 A>G maps to ENST00000326857 C72C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr4:122722614 C>T maps to NM_001034194.1 R12R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr5:179201052 G>A maps to NM_014757.4 V742V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr8:18080419 T>C maps to NM_001160176.1 F350F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr8:125487508 C>T maps to NM_007218.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-A4TM-01A-11D-A31X-10 chr9:36209296 C>T maps to NM_007096.3 F173F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:6512053 C>T maps to NM_031475.2 P741P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:16261248 C>A maps to NM_015001.2 P2838P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:19467300 G>T maps to ENST00000375267 L2858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:21050181 G>T maps to ENST00000444387 S296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:23761045 C>A maps to NM_017707.3 V605V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:54502288 G>T maps to ENST00000371338 P281P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:97700431 G>T maps to NM_000110.3 L806L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:109270511 C>A maps to NM_001144937.1 A398A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:156714095 G>T maps to NM_001126050.1 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:175306792 G>T maps to NM_003285.2 P1135P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:182357739 G>T maps to NM_002065.5 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:205210854 C>A maps to NM_014858.3 R144R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:212522556 G>T maps to NM_006243.3 L300L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:235840463 C>A maps to NM_000081.2 A3655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:237872251 G>T maps to NM_001035.2 T3332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr10:1151129 C>A maps to ENST00000416775 S343S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr10:35896617 G>T maps to NM_153368.2 P59P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr10:71175704 G>T maps to NM_001057.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr10:89530785 C>A maps to NM_032810.2 G235*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr10:105794457 C>A maps to NM_000494.3 P1229P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:6048448 A>G maps to NM_001001917.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:6412711 C>A maps to NM_000543.4 L139L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:18022065 C>A maps to NM_012139.2 L162L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:44151603 G>T maps to NM_000401.3 V396V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:58723278 G>T maps to NM_080661.2 G261*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:65767116 C>A maps to NM_032325.2 E76*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:66476482 C>A maps to NM_006946.2 E361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:74559381 G>T maps to NM_182969.1 P494P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:102195333 C>A maps to NM_182962.1 R32R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:108178687 G>T maps to NM_000051.3 V1913V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:113103962 C>A maps to ENST00000316851 P538P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr11:133801591 C>A maps to NM_014987.1 L403L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:6127549 G>T maps to NM_000552.3 P1678P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:56088249 C>A maps to ENST00000347027 L822L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:56088255 C>A maps to ENST00000347027 T820T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:62996743 C>A maps to NM_175895.3 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:104378525 G>T did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr14:37203758 C>A maps to NM_030631.3 G75*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr14:44975260 C>T maps to NM_032135.3 A310A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr14:90429931 G>A maps to NM_018319.3 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr15:31851375 G>T maps to ENST00000382902 R116R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr15:40656125 C>A maps to NM_033510.1 P140P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr15:43525499 C>A maps to NM_201631.3 L684L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr15:43766924 G>T maps to NM_001141980.1 R376R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr15:51207743 G>T maps to NM_007347.3 G108*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr15:63092914 C>A maps to NM_015059.2 R2142R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr15:99442746 G>T maps to NM_000875.3 E382*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr15:101597249 G>T maps to NM_024652.3 E1508*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr16:30735226 A>C maps to NM_006662.2 A1494A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr16:55855303 C>A maps to NM_001025195.1 A223A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr16:67702136 C>G maps to NM_001012984.2 Y196*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:1746131 C>A maps to NM_002945.3 P23P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:5009511 A>G maps to NM_014519.2 Y314Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:7750677 C>A maps to NM_001080424.1 R389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:41256153 G>T maps to ENST00000471181 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:46265268 C>A maps to NM_003726.3 S126S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:47781467 C>A maps to ENST00000415270 G254*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:48149436 G>T maps to NM_002204.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:73831765 G>T maps to ENST00000412096 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:74536234 C>A maps to NM_001077620.2 T4T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr18:3187545 C>A maps to NM_003803.3 T287T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:2222026 G>T maps to ENST00000221482 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:17405533 G>T maps to NM_024527.4 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:17942202 C>A maps to NM_000215.3 E938*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:36046407 G>T maps to NM_000704.2 P697P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:41306602 T>A maps to NM_053046.2 C42*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:49705257 C>A maps to NM_017636.3 P997P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr19:54653321 G>T maps to NM_014516.3 T478T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:3687898 C>A maps to ENST00000418971 P116P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:3744966 G>T maps to ENST00000403787 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:26698847 G>T maps to NM_194248.2 A975A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:43571343 G>T maps to ENST00000330266 S1421S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:64796764 G>T maps to ENST00000422803 T741T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:74742768 C>A maps to NM_016170.4 S137*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:131102986 G>T maps to NM_033416.1 G79*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:169814506 G>T maps to NM_003742.2 P770P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:202000721 G>T maps to NM_001127183.1 E139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:214149329 C>A maps to NM_024532.3 A41A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:219503379 G>T maps to NM_001105537.1 T1582T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:237172799 G>T maps to NM_212556.2 P63P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr2:238277575 C>A maps to NM_004369.3 G1510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:21337237 C>A maps to NM_012255.3 P711P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:35832360 G>T maps to NM_002951.3 E185*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:39803145 C>A maps to NM_002660.2 L1291L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:47641989 C>T maps to NM_006420.2 Y1632Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:48600832 C>T maps to NM_005985.3 C185C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:60485629 C>A maps to NM_001794.2 P447P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr20:60891784 C>T maps to NM_005560.3 L2566L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr21:41505891 C>A maps to NM_001389.3 E1151*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr21:41559169 G>T maps to NM_001389.3 P889P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr21:45978007 G>A maps to NM_198696.2 L197L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr22:32215149 C>A maps to NM_001136029.1 P603P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr22:38043466 C>A maps to NM_018957.3 R380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr22:40140199 G>T maps to NM_152512.3 L436L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr22:40807462 G>T maps to NM_020831.3 A909A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:40553891 G>C did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:49725330 C>A did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:107451867 G>T maps to NM_001142568.1 E223*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:122345836 C>A maps to NM_001113523.1 L465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:169706124 C>T maps to NM_003262.3 A236A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:190039983 C>A maps to NM_021101.4 A4A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:195006525 T>C maps to NM_012287.5 P745P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr3:196094967 C>A maps to NM_015562.1 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:36230646 G>T maps to NM_015230.2 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:76731614 G>T maps to NM_003715.2 E785*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:80246377 G>T maps to NM_032693.2 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:106157460 G>T maps to ENST00000513237 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:122853524 G>A maps to NM_001130698.1 S296S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:126329626 G>T maps to NM_024582.4 T1866T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:175577919 C>A maps to NM_006529.2 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr4:187530417 T>A maps to ENST00000260147 I3378I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr5:72800200 G>T maps to NM_001037637.1 G183*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr5:79375048 C>A maps to NM_003248.4 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr5:140562235 C>A maps to NM_020957.1 S34S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr5:150512076 C>A maps to NM_001155.4 G232G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr5:175395157 G>T maps to NM_032361.2 P18P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr5:177642284 C>T maps to NM_153373.2 G358G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr6:35967811 C>A maps to NM_052961.3 S134S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr6:43110026 C>A maps to NM_002821.3 L679L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr6:47678615 C>A maps to NM_153838.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr6:138632616 G>T maps to NM_020340.4 P1390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr6:149997820 G>T maps to NM_004690.2 P882P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr7:65445297 C>A maps to NM_000181.3 R103R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr7:92825187 C>A maps to ENST00000453812 G433*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr7:107808821 G>A maps to ENST00000379032 S1071S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr7:111617281 G>T maps to ENST00000428084 L202L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr8:3141756 C>A maps to NM_033225.5 P1354P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr8:61654761 T>C maps to NM_017780.2 H257H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr8:124988293 C>A maps to NM_001039112.2 P280P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr9:13136143 C>A maps to ENST00000319217 G1444*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr9:79328526 C>A maps to NM_015225.2 P289P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr9:117050769 C>A maps to NM_032888.2 P1341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr9:117240874 C>A maps to NM_015404.3 R265R. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GL-6846-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr9:133901682 G>T maps to ENST00000355048 E129*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr9:140943669 T>C maps to ENST00000277549 L1206L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chrX:47065803 C>A maps to NM_153280.2 T633T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chrX:71425049 G>T maps to NM_017669.2 P1189P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chrX:99946147 C>A maps to NM_001129896.2 E200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chrX:128710357 G>T maps to NM_000276.3 S648S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:43828620 G>A did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:111862961 C>T maps to NM_201653.2 N435N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:192128418 C>T maps to NM_130782.2 S63S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr1:232649813 A>T maps to NM_020808.3 I424I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr10:16941135 A>G maps to NM_001081.3 P2819P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr10:103454328 G>C maps to ENST00000331272 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:1643278 C>T maps to ENST00000359229 G15G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:58978385 A>T maps to NM_001039396.1 G651G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:63885634 G>A maps to NM_013280.4 E632E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:65835794 C>A maps to NM_006842.2 A869A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr11:113288846 C>T maps to ENST00000355319 E99E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:11420474 A>G maps to NM_006249.4 P236P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:29469909 T>A maps to NM_018099.3 Y364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:40758850 A>G maps to NM_198578.3 L2463L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:112036796 C>T maps to NM_002973.3 Q174Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr13:23927926 G>T maps to NM_014363.4 R728R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr13:52548875 G>A maps to NM_000053.2 S160S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:24709983 G>C maps to NM_001099274.1 A234A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:65008124 G>A maps to NM_021979.3 L186L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr14:101012902 G>A maps to NM_020836.3 H37H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr15:51790749 T>G maps to NM_001174116.1 S1557S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr15:73843451 A>G maps to NM_001042367.1 Q169Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr15:74327952 G>A maps to NM_033239.2 R717R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr17:42228327 G>C did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr19:10081315 G>T maps to NM_015719.3 P1306P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr19:35250174 C>A maps to NM_001007248.2 E511*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr19:42863079 G>T maps to ENST00000251268 E1773*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr19:49360677 C>A did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr19:56200302 G>T maps to NM_001130071.1 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:33482544 C>A maps to ENST00000354476 R788R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:97428004 C>A maps to NM_020184.3 Y423*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:179599139 A>G maps to NM_133378.4 F3893F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:182543428 C>A maps to NM_002500.2 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:197889958 T>C maps to NM_001195144.1 E561E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr2:203848265 A>G maps to NM_024744.14 Q699Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr20:43933411 C>A maps to ENST00000372754 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr20:44676667 G>T maps to NM_001134771.1 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:38316609 C>A maps to NM_004256.3 T256T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:48266892 T>C maps to NM_004345.3 L164L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:62317064 T>A maps to NM_020685.3 V81V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:98309566 A>T maps to NM_000097.5 A240A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:138664541 C>A maps to NM_023067.3 P341P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr3:146167109 C>T maps to ENST00000497985 K249K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr4:76529104 T>A maps to ENST00000307465 K231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr5:7878201 G>T maps to NM_024010.2 E210*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:29797252 G>A maps to ENST00000376828 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:71003974 G>A maps to NM_001851.4 D197D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:82461789 T>G maps to ENST00000369756 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr6:90660213 G>A maps to NM_001170794.1 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr7:95818644 C>T maps to NM_001160210.1 E298E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr7:141764247 C>A maps to ENST00000475668 L1470L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr9:92007356 A>T maps to NM_006378.3 Y201*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr9:102730747 G>A maps to NM_017919.2 V234V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr9:133759485 G>A maps to NM_007313.2 L622L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chrX:46401550 T>A did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chrX:122801089 A>G maps to NM_001081550.1 L353L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chrX:130217916 C>A maps to NM_144967.3 R177R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chrX:152826335 C>T maps to NM_001001344.2 F1014F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:12919094 A>C maps to NM_023014.1 P77P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:16332729 C>A maps to NM_178840.2 P133P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:155451418 T>C maps to ENST00000368346 A414A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:158517502 A>T maps to NM_001005189.1 I131I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr1:241663811 G>A maps to NM_000143.3 Q439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr11:134241358 A>G maps to NM_138342.3 T467T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr12:53671298 G>T maps to NM_012291.4 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr12:132395296 C>T maps to NM_003565.2 S300S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr14:59965597 G>C maps to ENST00000356057 V218V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr15:25207296 C>T maps to NM_022804.2 H17H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr15:70987422 C>T maps to NM_018003.2 K78K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr15:73660575 G>C maps to NM_005477.2 L12L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr17:6531559 G>A maps to NM_014804.2 Q199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr17:77710871 C>T maps to NM_178543.3 H353H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr19:50939281 G>T maps to NM_004533.3 V70V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:88890365 C>T maps to NM_004836.5 K324K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:166201261 C>G maps to NM_001040142.1 L920L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:168105758 G>A maps to NM_152381.5 R2619R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:179598481 C>A maps to NM_133378.4 G3968*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr2:220074989 G>A maps to NM_005689.2 I794I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr21:48083429 G>A maps to NM_206962.1 W411*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr5:9629373 G>A maps to NM_019599.2 F257F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr5:45461991 G>A maps to NM_021072.2 Q323*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr5:132161118 C>T maps to NM_001172700.1 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr7:142561392 A>T maps to NM_004445.3 V35V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr8:139767733 T>C maps to NM_152888.1 K656K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chr9:36339771 C>A maps to NM_022781.4 E509*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7966-01A-11D-2201-08 chrX:152823736 C>T maps to NM_001001344.2 A867A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr1:27332863 G>A maps to NM_052943.3 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr1:115280130 A>G maps to NM_001007553.1 G121G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr10:124740204 A>G maps to NM_153336.2 R70R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr11:1253367 C>A maps to ENST00000447027 P610P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr14:35295322 A>G maps to NM_013448.2 H144H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr15:52606370 T>C maps to ENST00000358212 P1813P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr16:23848698 C>T maps to NM_002738.6 G59G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr16:88653084 C>T maps to ENST00000452588 F227F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr17:7750210 A>C maps to NM_001080424.1 P262P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr18:48331526 A>G maps to NM_001127176.1 D156D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr18:56056372 T>C maps to NM_001144967.1 I868I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:2290212 C>T maps to NM_001101391.1 P521P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:7075687 C>G maps to NM_024341.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:13346024 G>A maps to NM_023035.2 Q1715*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:18499141 C>A maps to NM_004864.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:39058442 C>T maps to NM_000540.2 P4515P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:45868314 G>A maps to NM_000400.3 H154H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr19:49464329 T>C maps to NM_004324.3 Y211Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr2:54176407 A>G maps to NM_014614.2 L85L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr20:2776795 C>G maps to NM_019609.4 L418L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr22:30413917 G>T maps to NM_021090.3 V559V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr3:38404483 C>G maps to NM_005108.3 V89V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr3:178785386 C>A maps to NM_022470.3 E52*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr5:115822557 G>A maps to ENST00000257414 C283C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr6:29797246 C>T maps to ENST00000376828 T229T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr8:95262645 G>A maps to NM_181702.2 S261S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr8:144997532 C>G maps to NM_201380.2 L2325L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr8:145066936 G>A maps to NM_001009184.1 A348A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr9:35869822 C>T maps to NM_001004487.1 T192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr9:125751641 C>T maps to NM_012197.3 V219V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:11270888 G>A maps to NM_004958.3 L1212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:38288351 G>T maps to NM_005955.2 S403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:41107441 C>T maps to NM_014747.2 K52K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:150551616 C>T maps to NM_021960.4 E130E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:151372468 G>A maps to NM_002796.2 V51V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:186024753 T>A maps to NM_031935.2 V2364V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr1:215820885 G>T maps to ENST00000366943 I4923I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr11:60609626 G>T maps to NM_024098.3 R10R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr11:93911575 C>G maps to NM_015368.3 Y121*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr12:7125632 C>T maps to NM_005768.5 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr14:102689210 T>A maps to NM_181291.1 T579T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr15:40284410 G>A maps to NM_001013703.2 L889L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr15:73735651 G>T maps to NM_001042367.1 L42L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr19:44792843 T>C maps to NM_004234.4 V248V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr2:239162230 G>A maps to NM_022817.2 T811T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr20:2639398 A>C maps to NM_006899.2 *386E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr22:36877706 G>A did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr3:195506330 T>A maps to NM_018406.5 S4040S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr5:132342535 T>G maps to ENST00000509437 R62R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr6:122777746 A>G maps to NM_020755.2 L84L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr7:21469334 T>C maps to NM_003112.3 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chr9:75355126 T>C did not map to a codon.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chrX:20222170 G>A maps to NM_004586.2 A98A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chrX:70316473 C>T maps to NM_005938.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A4EM-01A-11D-A25F-10 chrX:110987896 G>T maps to NM_001099922.2 V899V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:146747122 C>A maps to NM_004284.3 G459G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:155313420 G>A maps to ENST00000368346 R2703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:156107473 A>C maps to NM_170707.2 S546S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:64968539 A>G maps to NM_032776.1 F963F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:74810905 G>A maps to NM_000917.3 Q269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr10:88911775 C>G maps to ENST00000298786 S222*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:44079984 C>T maps to NM_001031854.2 L482L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:108381025 T>G maps to NM_015065.2 T1736T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr11:119182660 T>A did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr12:64521383 C>G maps to NM_020762.2 S807*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr12:78591181 G>C did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr12:111926344 A>G maps to NM_002973.3 V885V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr14:24030556 T>C maps to NM_003917.2 P647P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr16:67487538 G>A maps to NM_004691.4 I70I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr17:66440667 C>T maps to NM_017983.5 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr18:20562276 G>A maps to ENST00000360790 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr19:49714006 G>T maps to NM_017636.3 T1123T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr19:54669260 G>T maps to NM_001145303.1 S285S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr2:84846835 T>G maps to NM_001370.1 L1200L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr2:152390039 G>T maps to NM_001164508.1 A7111A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr20:61300282 G>A maps to NM_016354.3 G626G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:14559361 G>A maps to ENST00000507975 C456C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:48338259 C>T maps to NM_005793.3 L58L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:50513566 G>T maps to ENST00000435965 G90G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:52505968 C>T maps to NM_007184.3 F183F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr3:132196968 T>C maps to NM_015268.3 I898I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-GL-A59R-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr5:6600167 G>A maps to NM_017755.5 T725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr5:13814811 C>A maps to NM_001369.2 E2378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr6:13230365 C>A maps to NM_030948.1 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr6:30954602 G>A maps to NM_001010909.2 T217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr8:41547821 G>A maps to ENST00000415018 L1343L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr8:81412102 T>C maps to NM_001105539.1 S449S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr9:32459419 G>T maps to NM_014314.3 C810*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:154033033 T>C maps to NM_207308.2 E944E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:155172113 G>A maps to NM_007112.3 R346*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr1:176525850 G>A maps to NM_020318.2 G131G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr10:7811177 C>T did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr10:100177416 G>A maps to NM_000195.2 A669A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr10:101559079 G>A maps to NM_000392.3 L328L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr11:82560213 T>C maps to NM_199418.2 P287P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:6637491 T>C maps to NM_014865.3 A1099A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:50847397 T>C maps to ENST00000429001 Y326Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:88514779 A>C maps to NM_025114.3 Y451*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:99640157 G>A maps to NM_152788.3 S747S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr12:120428097 C>T maps to NM_207311.2 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr16:2550435 G>T maps to ENST00000434757 L490L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr17:37821722 G>A did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr17:38978228 G>A maps to NM_000421.3 I203I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr17:79478135 T>C did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr19:11558369 G>A maps to ENST00000436195 E322E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr19:58084872 A>T maps to NM_017879.1 C133*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr2:163046172 A>G maps to NM_004460.2 D514D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr2:234749355 G>C maps to NM_018410.3 G690G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr20:633660 A>G maps to NM_080725.1 L57L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr21:27328003 G>C maps to NM_000484.3 T508T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr22:46654193 G>A maps to NM_006071.1 Q1676*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:33415409 C>T maps to NM_012157.3 C218C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:56649977 A>C maps to NM_001141947.1 A580A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:113795753 A>G maps to ENST00000485050 S249S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:122437695 A>G maps to NM_017554.2 T1566T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:160119802 T>C maps to NM_005496.3 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr3:179322635 G>A maps to NM_002492.2 S11S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr4:17710844 G>T maps to NM_015688.1 G188G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr4:68930402 C>A maps to NM_207407.2 G339*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr4:184129217 C>T maps to ENST00000448232 Y118Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr4:185552221 G>T maps to NM_032991.2 A191A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr5:1093743 C>A maps to NM_006598.2 V82V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr6:84563844 C>T maps to NM_001009994.1 A68A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr7:47698324 G>A maps to NM_001123065.1 L35L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr7:92083892 A>G maps to NM_021167.3 R171R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr8:95884141 A>G maps to NM_017864.2 A815A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr9:5126751 T>C maps to NM_004972.3 A1120A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr9:131370208 G>T maps to NM_001130438.2 G1409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chr9:134505711 C>T did not map to a codon.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chrX:10062248 A>T maps to NM_015691.3 V195V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-A59T-01A-21D-A28G-10 chrX:53584382 A>G maps to ENST00000276009 T2722T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:6206742 G>T maps to NM_015557.2 S524S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:11579474 C>A maps to NM_020780.1 P651P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:12058934 G>T maps to NM_014874.3 T236T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:15978292 C>A maps to NM_032341.4 A362A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:19500941 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:20233042 C>A maps to NM_015207.1 T318T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:20490552 G>T maps to NM_001105572.1 P128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:24663602 G>T maps to NM_021180.3 P221P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:36762297 C>A maps to NM_005119.3 R744R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:38289484 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:44019469 G>T did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:45810997 C>A maps to NM_007170.2 G410G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:45974494 C>A maps to NM_015506.2 R153R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:48877258 C>A maps to NM_019073.2 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:65139110 G>T maps to ENST00000371073 T897T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:65301898 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:78189056 C>A maps to NM_015017.3 G481*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:115430312 G>T maps to NM_003176.2 L419L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:119619161 C>A maps to NM_015836.3 L53L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:153914749 C>A maps to NM_014856.2 G241G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:154067512 C>A maps to NM_207308.2 A695A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:160326496 C>A maps to NM_015331.2 R583R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:161043547 G>T maps to NM_030916.2 R399R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:192992160 G>T maps to ENST00000367450 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:203680110 C>A maps to NM_001001396.1 R636R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:204515935 G>T maps to NM_002393.3 V278V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:205904849 C>A maps to NM_134325.2 V33V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:217622645 C>A maps to NM_018040.2 T437T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:234743437 G>T maps to NM_182972.2 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:235840463 C>A maps to NM_000081.2 A3655A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr1:247051803 G>T maps to ENST00000428671 P758P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:394702 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:910098 C>A maps to NM_015155.1 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:13655838 C>A maps to NM_003675.3 T226T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:76430023 G>T maps to NM_006721.2 G321*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:79569481 C>A maps to NM_004747.3 A1490A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:88451694 C>A maps to NM_001171610.1 P312P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:89264845 C>A maps to NM_004897.4 P58P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:90499787 G>T maps to NM_001080518.1 A284A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:102286731 C>A maps to NM_005004.2 P104P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:114154814 C>A maps to NM_016234.3 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:116014800 C>A maps to NM_198496.1 P85P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr10:133784251 G>T maps to NM_004052.2 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr11:4623626 G>T maps to NM_018073.5 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr11:7670376 G>T did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr11:45919734 C>A maps to NM_005456.2 S67S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr11:62291913 G>T maps to NM_001620.1 P3325P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr11:62401840 C>A maps to NM_198335.2 S189S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr11:70332266 C>A maps to ENST00000338508 A1371A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr11:72418366 C>A maps to NM_001040118.2 G526*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr11:74554953 C>A maps to NM_182969.1 L690L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr11:75173904 G>T maps to NM_030792.6 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr11:113265692 C>A maps to NM_178510.1 R175R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr11:124738764 C>A maps to NM_022370.3 S76S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:7593798 C>A maps to ENST00000416109 V25V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:8212673 C>A maps to NM_004054.2 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:12967117 C>A maps to NM_016355.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:13243542 G>T maps to NM_001080555.1 T86T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:18534753 C>A maps to NM_004570.4 P604P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:52284611 C>A maps to NM_182608.3 P294P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:53240600 C>A maps to NM_173352.2 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:55420843 G>T maps to NM_021191.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:85677440 C>A maps to NM_006982.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:117161027 C>A maps to NM_024738.1 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:119926638 C>A maps to NM_178499.3 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:121465599 G>T maps to NM_003733.2 P226P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr12:125441352 G>T maps to NM_032656.3 P779P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr13:41373269 C>A maps to NM_014252.3 R45R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr13:44411565 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr13:52639629 C>A maps to NM_199289.1 T680T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr13:98865555 G>A maps to NM_005766.2 S20S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:20404274 G>T maps to NM_001004063.2 A150A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:20846218 C>A maps to NM_007110.4 A1895A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:21215993 G>T maps to NM_006683.4 G85G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:24601869 C>A maps to NM_203402.2 T239T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:24801007 C>A maps to NM_139247.3 E219*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:50360606 G>T maps to NM_001663.3 T51T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:52174909 C>A maps to ENST00000344768 R225R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:53360016 C>A maps to NM_001134999.1 G174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:55617543 G>T maps to NM_014750.4 L797L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:69853681 C>A maps to NM_004450.2 L70L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:70246023 G>T maps to NM_003049.3 A207A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:74454714 C>A maps to NM_001249.2 E31*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:100119078 C>A maps to NM_001127258.1 P258P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr14:105716669 G>T maps to NM_033271.2 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:34072504 C>A maps to NM_001036.3 L3077L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:43512963 G>T maps to NM_000119.2 P20P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:43820042 C>A maps to ENST00000382031 S2362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:45386774 C>A maps to NM_014080.4 E1504*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:48787386 G>T maps to NM_000138.4 T870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:48812886 G>T maps to NM_000138.4 V372V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:50528291 G>A maps to NM_003645.3 *621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:50546855 C>A maps to NM_002112.3 T149T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:55790434 C>A maps to NM_130810.2 T31T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:60644644 C>A maps to NM_001002858.2 G225*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:65209586 G>T maps to NM_182703.3 V47V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:85327288 C>A maps to NM_014630.2 P461P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:89422414 C>A maps to NM_178232.2 A193A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:89760521 G>T maps to NM_000326.4 R59R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:99500553 C>A maps to NM_000875.3 P1329P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr15:102215847 C>A maps to NM_152334.2 P581P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:2815013 G>T maps to NM_016333.3 P1495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:2815727 G>T maps to NM_016333.3 P1733P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:10567845 G>T maps to NM_024997.2 E517*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:11875280 C>A maps to NM_014153.3 A36A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:19195459 C>A maps to NM_016524.2 P314P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:20486734 C>A maps to NM_001010845.2 R316R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:27441433 C>A maps to NM_181079.4 L36L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:27472808 G>T maps to NM_001520.3 P2064P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:57075911 G>T maps to NM_032206.3 L1016L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:58757681 C>A maps to NM_002080.2 G72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:66949282 T>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:67314183 G>T maps to NM_001129729.1 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:70504932 C>A maps to NM_145059.2 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:71610123 C>A maps to NM_000353.2 V65V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:75204187 C>A maps to NM_153688.2 R394R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:77228709 G>T maps to NM_014940.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:80718714 G>T maps to NM_152342.2 P112P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:81390560 C>A maps to NM_022041.3 R269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:88068945 C>A maps to NM_001173543.1 L395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:88688703 C>A maps to ENST00000452588 P549P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr16:88926306 C>A maps to NM_016209.3 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:1943866 C>A maps to NM_001383.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:7318874 C>A maps to NM_020795.2 P361P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:7611342 C>A maps to NM_001406.3 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:9596448 G>T maps to NM_153210.3 L453L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:18881090 G>T maps to NM_001039999.2 R630R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:28384836 G>T maps to NM_198529.3 E837*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:36552249 G>T did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:38433419 C>A maps to NM_133264.4 P422P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:41197783 G>T maps to ENST00000471181 R1857R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:43011404 G>T maps to ENST00000438933 L316L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:47218740 G>T maps to NM_153446.2 P109P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:48149436 G>T maps to NM_002204.2 A349A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:49048170 C>A maps to ENST00000376407 T1250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:56638923 C>A maps to ENST00000240361 E1418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:76563098 G>T maps to ENST00000389840 P478P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:78264395 C>A maps to NM_020914.4 T429T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr17:80881598 C>A maps to NM_005993.4 P750P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr18:31318453 G>C maps to NM_030632.1 L362L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr18:55287842 C>A maps to NM_004539.3 T17T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:5456678 C>A maps to NM_181710.3 R393R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:6750376 C>A maps to ENST00000313244 P490P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:14076474 C>A maps to NM_002918.4 V692V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:18376584 C>A maps to NM_001145304.1 G589*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:21990818 C>A maps to NM_003423.2 G674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:33355185 G>T maps to NM_014270.4 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:37618798 C>A maps to NM_144689.3 T302T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:38966066 G>T maps to NM_000540.2 E1424*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:41174043 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:46032613 C>A maps to NM_001017989.2 A81A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:51412560 C>A maps to NM_004917.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:55697670 C>A maps to NM_002842.3 V900V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:57910486 G>T maps to NM_001172773.1 E290*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:26683821 G>T maps to NM_194248.2 T1870T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:27322575 C>A maps to NM_006488.2 A285A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:27456642 C>A maps to NM_004341.3 P1122P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:27716949 G>T maps to NM_022823.2 R101R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:32820110 G>T maps to NM_016252.3 L4504L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:54483006 G>T maps to NM_001003937.2 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:55467311 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:66670063 C>A maps to ENST00000407092 R172R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:73682418 C>A maps to NM_015120.4 S2556S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:74458395 C>A maps to NM_021196.3 T938T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:74683251 C>A maps to ENST00000452361 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:108624954 C>A maps to NM_021815.2 P310P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:133540393 G>T maps to NM_207363.2 P1330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:141283491 G>T maps to NM_018557.2 T2649T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:149837879 C>A maps to NM_004522.1 S458S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:179406206 C>A maps to NM_133378.4 G29965*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:179431646 G>T maps to NM_133378.4 T23836T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:179474446 G>T maps to NM_133378.4 R14667R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:179640548 G>T maps to NM_133378.4 T2014T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:192700828 C>A maps to NM_004657.5 S366S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:209176979 G>T maps to NM_015040.3 G553*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:210558771 C>A maps to NM_002374.3 S626S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:215819925 C>A maps to NM_173076.2 P2131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:219254616 C>A maps to NM_000578.3 R274R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:219920489 C>A maps to NM_002181.3 P225P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:223161799 G>T maps to NM_181459.3 S73*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:233655499 C>A maps to ENST00000373566 R291R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:237489920 G>T maps to NM_020311.2 A271A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:238004495 C>A maps to NM_006710.4 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:238486775 C>A maps to NM_022449.3 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:239013306 C>A maps to NM_194312.2 R166R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:23065770 G>T maps to NM_012072.3 P353P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:44569769 C>A maps to NM_022104.3 P199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:45022173 G>T maps to ENST00000439931 T62T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:45195023 C>A maps to NM_022829.5 S446S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:54579047 C>A maps to NM_080617.4 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:57767921 C>A maps to NM_178457.1 S616S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:62070958 G>A maps to NM_172107.2 L307L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr21:38604679 C>A maps to NM_006052.1 E169*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr21:47330826 C>A maps to NM_020528.2 A161A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr21:47924304 G>T maps to ENST00000318711 T230T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr21:48064351 C>A maps to NM_206962.1 P93P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr22:17589522 G>T maps to NM_014339.5 G472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr22:24582268 G>T maps to NM_019601.3 E510*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr22:26937377 C>A maps to NM_003595.3 V73V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr22:30886108 G>T maps to NM_174977.3 P402P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr22:31043002 C>A maps to NM_001001479.2 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr22:40711446 C>A maps to ENST00000454349 P1627P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr22:42276947 C>A maps to NM_004599.2 R664R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr22:46238910 C>A maps to NM_013236.3 T426T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr22:47059986 C>A maps to NM_015124.2 S230S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr3:4687298 G>T maps to ENST00000356617 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr3:4726880 C>A maps to ENST00000356617 P1227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr3:38357175 C>A maps to NM_004803.3 T502T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr3:47030652 G>T maps to NM_015175.1 A116A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr3:51749379 C>A maps to NM_000839.3 R531R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr3:52386587 C>A maps to ENST00000273600 S964S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr3:67659947 C>A maps to NM_003848.3 G53*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr3:115805255 C>A maps to NM_002338.3 V101V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr3:124807170 G>T maps to NM_001195483.1 L655L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr3:182810333 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr3:193175209 C>A maps to NM_032279.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:1165715 C>A maps to NM_012445.3 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:2087471 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:2906684 G>T maps to NM_014189.2 R452R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:3475235 C>A maps to ENST00000389653 G68G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:15964214 G>T maps to NM_031950.3 R180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:25156759 C>A maps to NM_016955.3 V187V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:79229220 C>A maps to NM_025074.6 V512V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:81123122 C>A maps to NM_001099403.1 P169P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:100003126 C>A maps to NM_000671.3 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:104117195 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:110639867 C>A maps to NM_030821.4 G86*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:113189564 G>T maps to NM_018569.4 *303Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr4:134075509 C>A maps to NM_032961.1 R894R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr5:37022235 C>A maps to NM_133433.3 P1804P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr5:80109401 G>T did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr5:87516501 C>A maps to NM_153354.3 V108V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr5:112420914 G>T maps to NM_001085377.1 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr5:112860746 C>A maps to NM_022828.3 T116T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr5:130846178 C>A maps to ENST00000514667 T261T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr5:140432356 C>A maps to NM_013340.2 A434A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr5:141694316 G>T maps to NM_030964.3 P142P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr5:147030068 C>A maps to NM_014790.3 L223L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr5:147784246 G>T did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:4935968 C>A maps to ENST00000328908 S358S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:24667518 G>T maps to NM_018473.3 E10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:26509105 G>T maps to NM_001732.2 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:28094667 G>T maps to NM_025231.1 L165L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:32190525 G>T maps to NM_004557.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:36068010 C>A maps to NM_001315.2 P243P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:43112986 G>A maps to NM_002821.3 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:53160467 G>T maps to ENST00000370918 T10T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:56846640 C>A maps to NM_152731.2 T11T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:73834212 G>T maps to NM_001160133.1 E409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:136590750 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr6:160169380 C>A maps to NM_004906.3 A144A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr7:1513940 C>A maps to ENST00000389470 E2112*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr7:8126021 C>A maps to NM_138426.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr7:88962751 C>A maps to NM_181646.2 P152P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr7:107431531 C>A maps to NM_000111.2 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr7:138601770 G>T maps to NM_001164665.1 G867G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr7:142569677 G>T maps to NM_018646.2 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:2024233 G>T maps to NM_003970.2 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:27328545 G>T maps to NM_000742.3 S10S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:35541165 G>T maps to ENST00000416672 S224S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:37991054 C>A maps to NM_004674.3 P537P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:41467378 C>T maps to NM_178819.3 S147S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:67592143 C>A maps to NM_019607.1 S145S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:73932952 C>A maps to NM_017489.2 P150P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:100533187 C>A maps to NM_017890.3 P1590P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:126448583 C>A maps to NM_025195.2 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr8:145700318 C>A maps to NM_003923.2 G134*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:317092 G>T maps to NM_203447.3 L264L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:4706078 A>G maps to NM_017913.2 E327E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:33295193 C>A maps to NM_002504.4 R268R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:35607969 C>A maps to NM_006285.2 R253R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:35750257 C>A maps to ENST00000456972 A85A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:113562827 C>A maps to ENST00000189978 R730R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:115421589 C>A maps to NM_133465.2 T464T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:116151935 C>A maps to ENST00000277315 G228G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:124064368 G>T maps to NM_000177.4 T91T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:125288876 C>A maps to ENST00000359439 V233V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:129453226 G>T maps to NM_001174147.1 E147*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:131262516 C>A maps to NM_153435.1 R889R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:133936530 C>A maps to ENST00000355048 P756P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:138588479 C>A maps to NM_001101677.1 R213R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:140507360 C>A maps to NM_152285.2 T44T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:21996163 G>T maps to NM_004595.3 G198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:32360315 G>T maps to ENST00000357033 A1941A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:41554942 C>A maps to NM_005300.3 S19S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:47104815 C>A maps to NM_004651.3 P778P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:48385410 C>A maps to NM_006579.2 I112I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:56292170 G>T maps to NM_007250.4 G214*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:69496296 G>T maps to NM_004312.2 L120L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:70674084 G>T maps to ENST00000449580 E1606*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:70823663 C>A maps to NM_052957.4 P179P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:76845316 G>T maps to NM_000489.3 P2068P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:103080489 G>T maps to NM_016370.2 P75P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:133609214 G>T maps to NM_000194.2 E47*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:134294441 G>T maps to NM_001031705.2 P106P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chrX:153706713 C>A maps to NM_006014.3 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:2066716 G>T maps to NM_002744.4 R117R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:3418387 C>A maps to ENST00000452816 P837P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:6188973 C>A maps to NM_015557.2 S1181S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:6324671 C>A maps to NM_007274.3 A366A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:8390575 C>A maps to ENST00000377479 P375P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:8925416 G>T maps to NM_001428.2 P264P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:11562816 C>A maps to NM_020780.1 S393S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:15545872 C>A maps to NM_018022.2 P132P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:15904350 C>A maps to NM_024758.3 R243R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:17350502 C>A maps to NM_003000.2 G203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:24078343 C>A maps to NM_003198.2 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:26899812 C>A maps to NM_001006665.1 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:27215511 G>T maps to NM_018066.3 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:28136755 G>T did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:28857038 G>T maps to NM_001048194.2 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:35260284 C>A maps to NM_002060.2 A157A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:38040015 G>T maps to NM_013285.2 L448L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:39875951 C>A maps to NM_015038.1 L5L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:43637244 C>A maps to NM_001159936.1 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:44595270 C>A maps to NM_173484.3 R110R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:45798127 C>A maps to NM_001128425.1 R241R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:51171559 G>T maps to NM_007051.2 A185A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:51860119 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:52520711 G>T maps to NM_015913.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:63307214 C>A maps to NM_032852.2 T402T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:63920060 G>T maps to ENST00000371092 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:67861345 C>A maps to NM_001559.2 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:85648160 G>T maps to NM_032184.1 R722R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:120459313 C>A maps to NM_024408.2 E2011*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:150443655 C>A maps to NM_015203.3 S744S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:150722647 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:153751266 C>A maps to ENST00000271857 R646R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:155182009 G>T maps to NM_002455.3 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:155226563 C>A maps to NM_005698.2 L266L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:156539180 C>A maps to NM_178229.4 E38*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:156818723 G>A maps to NM_014215.2 Y520Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:160385926 C>A maps to NM_020335.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:160968874 C>A maps to NM_016946.4 S274S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:161695809 G>T maps to NM_001002901.2 S169S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:162353016 C>A maps to NM_001135240.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:169819405 G>T maps to NM_018186.2 G722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:180031393 C>A maps to NM_014810.4 R1768R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:185269244 C>A maps to NM_006469.4 G463*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:200944785 C>A maps to NM_017596.2 L1472L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:203465360 C>A maps to NM_014359.3 P76P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:203800888 C>A maps to NM_014827.4 S267S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:209965731 C>A maps to NM_006147.2 V183V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:210194390 C>A maps to NM_001146261.1 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:224491559 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:228471282 G>T maps to NM_001098623.1 T2939T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr1:236729957 G>T maps to NM_018072.5 A1432A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:486817 G>T maps to NM_014974.2 T129T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:15648405 G>T maps to NM_003638.1 R594R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:50944566 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:71148969 G>T maps to ENST00000439900 V686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:75877914 C>A maps to NM_014000.2 P1131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:75898089 T>C maps to NM_207012.2 L16L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:93244389 C>A maps to ENST00000446394 A320A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:98985889 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:102056006 C>A maps to NM_016112.2 E410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:102822630 C>A maps to NM_030929.4 P94P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr10:135099015 C>A maps to NM_006659.2 L613L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:1098667 G>A maps to ENST00000441003 V2346V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:1248330 C>A maps to ENST00000447027 R178R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:6023762 G>T maps to NM_001005179.2 R206R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:17527376 C>A maps to NM_153676.3 L711L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:35323076 G>T maps to NM_004171.3 I282I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:57076185 C>T maps to NM_033396.2 G1333G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:57463495 C>A maps to NM_015457.2 L330L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:61039193 C>A maps to NM_152718.2 G580*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:61908497 C>A maps to NM_001040694.1 P525P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:62327281 C>A maps to ENST00000378019 E445*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:62341308 C>A maps to NM_001404.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:62458268 G>T maps to NM_001130702.1 P381P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:62648665 G>A maps to NM_001012661.1 A189A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:64010735 C>A maps to NM_057092.2 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:64119643 C>A maps to NM_032251.5 R1048R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:66103846 C>A maps to NM_004292.2 A9A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:66595792 C>A maps to ENST00000360962 T543T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:74414448 C>A maps to NM_015424.3 E283*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:94278255 C>A maps to NM_002033.3 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:114118001 G>T maps to NM_001018011.1 T569T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:124908464 C>A maps to NM_025004.2 T850T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr11:125853986 C>A maps to ENST00000392693 V925V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr12:6936290 G>T maps to NM_019858.1 T563T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr12:7475897 C>A maps to NM_001080454.1 P398P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr12:7548961 C>A maps to ENST00000416109 S603S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr12:10321694 G>T maps to NM_002543.3 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr12:27799018 G>T maps to NM_003622.3 G99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr12:49364267 C>A maps to NM_003394.3 A15A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr12:109877434 G>T did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr12:111772332 C>A maps to NM_015267.3 S1005S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr12:111801083 C>A maps to NM_001177996.1 E63*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr12:112241719 G>T maps to NM_000690.2 S488S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr12:116429695 G>T maps to NM_015335.4 P1021P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr13:28130463 C>A maps to NM_153371.3 G485G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr13:29599441 C>A maps to NM_001033602.2 R213R. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr13:41767337 G>T does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr13:41941750 C>A maps to NM_024561.4 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr13:47354108 G>T maps to NM_001984.1 A187A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr13:51956176 G>T maps to NM_012141.2 P421P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr13:109779830 C>A maps to NM_015011.1 T1306T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr13:113964010 C>T maps to NM_005561.3 S79S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:21871371 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:24569411 C>A maps to NM_004563.2 P408P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:31074918 G>T maps to NM_017769.3 G407*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:32615478 C>A maps to NM_001030055.1 T1292T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:35242929 A>G maps to NM_013448.2 V1000V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:45636323 C>A maps to NM_020937.2 R654R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:96773253 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:103998967 C>A maps to ENST00000299201 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:105175647 G>T maps to ENST00000252520 R660R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr14:105517537 C>A maps to NM_013345.2 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:34544572 C>A maps to NM_133647.1 L377L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:40565819 G>T maps to NM_020168.4 V562V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:42434833 C>A maps to ENST00000397272 E743*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:55742565 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:60741049 C>A maps to NM_024611.4 G706*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:68434626 G>T did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:77769914 G>T maps to NM_018200.2 E212*. Only missense variants will be evaluated by CHASM.
Reference base specified for sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:79217689 C>A does not match reference base at that coordinate in hg19.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:81199121 C>A maps to NM_018689.1 P510P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:82533744 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:85164676 C>A maps to NM_181877.3 P417P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr15:91430243 G>T maps to NM_002005.3 R147R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:277240 C>A maps to NM_201412.1 T52T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:837590 G>T maps to NM_058192.2 P49P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:1828209 C>A maps to NM_080861.3 R139R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:2222336 C>A maps to NM_032271.2 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:4405297 C>A maps to NM_024535.3 E921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:28511046 C>A maps to NM_145659.3 R219R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:48210859 C>A maps to NM_032583.3 V1171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:57549315 G>T maps to NM_033212.3 S487*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:57601815 C>A maps to ENST00000349457 S290S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:57608897 G>T maps to ENST00000349457 L460L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:75238166 C>A maps to NM_001025200.3 V228V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:89246729 C>A maps to NM_004933.2 A108A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr16:89704483 G>T maps to NM_004413.3 E364*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:7474027 G>T maps to ENST00000321337 A503A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:16285475 C>G maps to NM_018955.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:27448109 C>A maps to NM_078471.3 L497L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:34068052 G>T did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:38182476 C>T maps to NM_014815.3 S639S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:40459442 C>A maps to NM_003152.3 Y568*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:41180502 C>A maps to NM_005440.4 R164R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:45893998 C>A maps to NM_145798.2 S286S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:48916888 C>A maps to NM_175575.5 P80P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:60501295 A>G maps to NM_181725.3 A11A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:61511912 G>A maps to NM_001915.3 N202N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:78087040 G>T maps to NM_001079804.1 E689*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:79913364 G>A maps to NM_178493.5 N348N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:80012539 G>T maps to NM_212492.1 E195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr17:80044323 G>T maps to NM_004104.4 R1180R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr18:14791413 G>T maps to NM_001145029.1 T583T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr18:28588038 C>A maps to NM_001941.3 E536*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr18:35145463 G>T maps to NM_020180.3 P47P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr18:48584504 C>A maps to NM_005359.5 A226A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr18:74154199 G>T maps to ENST00000443185 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:2112905 C>A maps to ENST00000355272 E914*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:2280905 C>A maps to NM_198532.2 E9*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:3600035 G>T maps to NM_201636.2 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:4354105 G>T maps to ENST00000262967 L243L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:5047536 G>T maps to NM_015015.2 V161V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:7623832 C>A maps to NM_001166111.1 S1175S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:10570335 G>T maps to NM_001111307.1 L422L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:13873863 C>A maps to NM_030818.2 S391S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:21240302 G>T maps to NM_025189.3 G397*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:34791741 G>T maps to NM_014686.3 E122*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:36211208 C>A maps to NM_014727.1 S320S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:36273702 G>T maps to ENST00000007510 A451A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:39207934 C>A maps to NM_004924.3 P374P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:39804830 G>T maps to NM_020862.1 P382P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:41711993 C>A maps to ENST00000301173 P432P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:41850654 C>A maps to NM_000660.4 G211*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:44030463 C>A maps to NM_014297.3 S88S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:45850755 G>T maps to NM_177417.2 E181*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:45851939 C>A maps to NM_177417.2 L272L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:45923610 C>A maps to NM_202001.2 L132L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:46627533 C>A maps to NM_207393.1 G24*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:47349270 G>T maps to NM_004069.3 A44A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:49867854 C>A maps to NM_014419.3 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:49937243 C>A maps to NM_020309.3 G233*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:51485077 C>A maps to NM_005046.2 G56*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:52569708 G>T maps to NM_001136499.1 R476R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:54545032 C>A maps to NM_198481.3 S197S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:55777315 C>A maps to NM_012267.4 L277L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr19:58232301 G>T maps to ENST00000335820 L384L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:9613122 G>T maps to NM_016207.2 E678*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:15319240 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:24262045 C>A maps to NM_025203.2 E107*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:30977230 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:54885164 C>A maps to NM_003128.2 A2075A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:69093079 C>A maps to NM_014482.1 G320*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:71303783 G>T maps to NM_017567.4 E286*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:86352174 C>A maps to NM_017952.5 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:95542465 C>A maps to NM_144705.2 A420A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:112779950 C>A maps to NM_006343.2 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:113940605 C>A maps to NM_012455.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:120005376 C>A maps to NM_182915.2 P215P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:121747290 C>A maps to NM_005270.4 P1267P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:163279986 C>A maps to NM_033272.2 S671S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:165994430 G>T maps to NM_006922.3 P783P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:170359687 G>T maps to ENST00000419050 V300V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:179473204 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:182413584 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:196682498 C>A maps to NM_018897.2 G3116*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:198011811 G>T maps to NM_001195144.1 T43T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:219296622 C>A maps to NM_007127.2 V382V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:220099701 G>T maps to NM_001042410.1 G453G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:230705590 G>T maps to ENST00000389044 P360P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:234354360 C>A maps to NM_152879.2 P429P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr2:241979577 G>T maps to NM_001080437.1 G378*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr20:4771168 C>A maps to NM_014737.2 V155V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr20:19955385 C>T maps to ENST00000255006 S288S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr20:32000229 C>A maps to NM_003098.2 L304L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr20:43348656 G>T maps to NM_003881.2 L60L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr20:44527046 C>A maps to NM_000308.2 A485A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr20:49626224 C>A maps to NM_002237.3 V217V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr20:51870591 C>A maps to NM_173485.5 R199R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr21:17250224 G>T maps to ENST00000285681 L1002L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr21:27071035 G>T maps to NM_021219.2 G148*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr22:17588621 G>T maps to NM_014339.5 G351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr22:17662807 G>T maps to NM_017424.2 A448A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr22:19707393 C>A maps to NM_002688.5 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr22:23631731 G>T maps to NM_004327.3 V877V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr22:26897975 C>A maps to NM_012143.2 G231*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr22:29913072 C>A maps to NM_003678.4 A542A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr22:30772605 G>T maps to NM_001017437.2 E711*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr22:38266326 C>A maps to ENST00000262832 R285R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr22:51017936 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:9517774 G>T maps to ENST00000407969 *1462Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:14941937 C>A maps to NM_152536.3 S1061S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:20164194 G>T maps to NM_003884.4 E438*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:31725582 C>A maps to NM_017784.4 L423L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:48618350 C>A maps to NM_000094.3 P1648P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:48691853 C>A maps to NM_001407.2 G1674*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:50971507 G>T maps to NM_004947.4 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:51675821 C>A maps to NM_015106.2 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:52378532 C>A maps to ENST00000273600 A438A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:52428929 G>T did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:52546924 G>T maps to NM_015136.2 E1037*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:100568928 C>A maps to ENST00000471714 L494L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:101390911 C>A maps to NM_014415.3 S152S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:130095659 C>A maps to ENST00000312481 A216A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:134323199 C>A maps to NM_178554.4 E403*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:164724670 C>A maps to NM_001041.3 G1447*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:184603939 C>T maps to ENST00000437079 R593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:949634 G>T maps to NM_032326.2 G267*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:3432653 C>A maps to NM_198229.2 P1362P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:4322631 G>T maps to NM_145291.3 S629S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:15627173 G>T maps to NM_012161.3 T517T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:57676350 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:66217147 G>T maps to NM_004439.5 R823R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:70596312 G>T maps to NM_014465.3 T228T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:71275518 C>A maps to NM_021225.4 P158P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:89668082 C>A maps to NM_014883.2 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:103226261 C>A maps to NM_001135146.1 G187*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:104012407 C>A maps to NM_020139.3 E95*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:119810280 C>A maps to NM_133477.2 P30P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:153896620 C>A maps to NM_033393.2 P726P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:154641344 G>T maps to ENST00000274068 S207S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:169158850 C>A maps to NM_017631.5 L1420L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr4:184931613 C>A maps to NM_020225.1 L541L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:1272337 C>A maps to NM_198253.2 E782*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:13751194 C>A maps to NM_001369.2 E3735*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:14397201 G>T maps to NM_007118.2 L1454L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:14756001 C>A maps to NM_054027.4 G162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:16474961 G>T maps to NM_001034850.1 S461*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:24535388 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:35654683 C>A maps to NM_024867.3 T278T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:50111270 C>A maps to ENST00000505697 T527T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:56176628 G>T maps to NM_005921.1 G727*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:56181765 G>T maps to NM_005921.1 S1330S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:61846258 C>A maps to NM_001134779.1 P812P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:82352970 C>A maps to NM_174909.4 E51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:82849186 C>A maps to NM_004385.4 T3166T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:94204109 C>A maps to NM_024717.4 L788L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:96215655 G>T maps to NM_001130140.1 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:110097442 C>A maps to NM_138773.1 T406T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:112487059 G>T maps to NM_001085377.1 L229L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:112769663 G>T maps to NM_032028.3 S291S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:126869469 G>T maps to ENST00000330542 G305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:140595878 C>A maps to NM_018933.2 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:140625664 T>C maps to NM_018935.2 S173S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:140779238 C>A maps to NM_018925.2 A515A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:149440497 G>T maps to NM_005211.3 S632S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:149907409 C>A maps to NM_001543.4 P186P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:158523374 G>T maps to NM_024007.3 R111R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:158524121 G>T maps to NM_024007.3 R51R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:176024787 G>T maps to NM_052899.2 S683*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr5:177632983 G>A maps to NM_031266.2 L117L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:24503525 C>A maps to NM_170740.1 L158L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:24503564 C>A maps to NM_170740.1 A171A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:31935748 C>A maps to NM_006929.4 T916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:34026769 G>T maps to NM_000841.1 P336P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:38883128 G>T maps to ENST00000327475 L3360L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:42147065 C>A maps to NM_000409.3 T177T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:46656737 G>T maps to NM_001010870.2 T291T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:51915027 C>A maps to NM_138694.3 G736*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:64422648 C>A maps to NM_015153.2 S1722*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:70745809 C>A maps to NM_001858.4 P383P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:70886438 G>T maps to NM_001858.4 G884*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:73110400 C>A maps to NM_014989.4 P1688P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:87795536 C>A maps to NM_000735.2 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:108233958 G>T maps to NM_007214.4 A178A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:109321801 G>T maps to NM_014454.1 P207P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:117737470 C>A maps to NM_002944.2 G60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:125112516 G>T maps to NM_001040214.1 V169V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:142738425 G>T maps to NM_198569.2 V985V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:144863953 C>A maps to NM_007124.2 T2181T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr6:154749270 G>T maps to NM_173515.2 T240T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:939111 G>T maps to NM_006869.2 R271R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:1534498 C>A maps to ENST00000389470 P749P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:5347895 C>A maps to NM_001080495.2 T2916T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:7278444 C>A maps to NM_020156.3 T260T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:21813430 C>A maps to NM_003777.3 T3057T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:27282681 G>T maps to NM_001989.3 L11L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:34979807 G>T maps to NM_015283.1 P534P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:36445997 C>A maps to NM_018685.2 T232T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:44573421 C>A maps to NM_013389.2 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:45112358 C>T maps to NM_001029835.2 T281T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:48313363 C>A maps to NM_152701.3 T1367T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:50450403 C>A maps to NM_006060.3 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:99621200 A>G maps to NM_003439.1 V24V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:99817649 G>T maps to NM_024070.3 A39A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:147336336 C>A maps to NM_014141.5 A679A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:149520901 C>A maps to NM_198455.2 A4497A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:150034576 C>A maps to NM_023942.2 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr7:150878301 C>G maps to ENST00000422024 L321L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr8:19276261 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr8:22005933 C>A maps to NM_139278.2 L462L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr8:25209257 G>T maps to NM_024940.6 A922A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr8:25225744 C>A maps to NM_024940.6 R1088R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr8:39691518 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr8:42940370 C>A maps to NM_002027.2 S362S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr8:72970051 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr8:133895164 G>T maps to NM_003235.4 T332T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr8:134239895 C>A maps to NM_003882.2 P349P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr8:140743317 C>A maps to NM_031466.5 E1243*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr8:145620370 C>A maps to NM_013291.2 E1072*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr9:17135236 G>T maps to NM_017738.2 V58V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr9:113096570 G>T maps to NM_001003936.2 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr9:113220819 C>A maps to ENST00000374463 A1169A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr9:115931543 C>A maps to ENST00000446284 G1174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr9:116172534 G>T maps to NM_017443.4 A13A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr9:119625887 G>T maps to ENST00000313400 R672R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr9:131221844 G>T did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr9:139616407 C>A maps to NM_152421.3 S78S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr9:140086933 G>T maps to NM_001128228.2 P645P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:215794 G>T maps to NM_018390.3 T255T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:16774810 C>A maps to NM_032796.3 P250P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:19564042 G>T maps to NM_031892.2 S540S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:19626103 G>T maps to NM_031892.2 P319P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:24228418 C>A maps to NM_003410.3 P448P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:34149264 C>A maps to NM_203408.3 A377A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:43637986 C>A did not map to a codon.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:47035948 C>A maps to NM_005676.3 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:53267444 C>A maps to NM_001111125.1 G1053G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:53589181 C>A maps to ENST00000276009 E2410*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:69712121 C>A maps to ENST00000194900 P580P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:73815739 G>T maps to NM_183353.2 R25R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:105970589 C>A maps to NM_194463.1 P149P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:106186404 C>A maps to NM_024657.4 P572P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:122756616 G>T maps to NM_001081550.1 G1259G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:128902400 C>A maps to NM_003399.5 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:130415840 G>T maps to NM_001170961.1 R442R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:132352071 C>A maps to NM_016521.2 V72V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:144906276 C>A maps to NM_001144010.2 T778T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chrX:153698077 C>A maps to NM_017514.3 A1582A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:1226705 G>T maps to NM_001130413.2 E611*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:1890603 C>A maps to ENST00000434971 T602T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:2341813 A>C maps to NM_153818.1 L63L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:9079291 G>T maps to NM_207420.2 R138R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:12059083 C>A maps to NM_014874.3 R250R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:21226357 C>A maps to NM_001198801.1 E554*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:22178287 G>T maps to NM_005529.5 A2334A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:22413229 C>G maps to NM_001039802.1 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:22413328 C>G maps to NM_001039802.1 V152V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:26612415 C>A maps to NM_183008.2 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:28354306 G>T maps to NM_001990.2 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:38187479 G>T maps to NM_001099439.1 L666L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:38338747 G>A maps to ENST00000373026 L761L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:42047171 C>A maps to NM_024503.3 P1099P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:43241040 C>A maps to NM_024097.2 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:44063473 C>T maps to NM_002840.3 V623V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:44063521 C>T maps to NM_002840.3 I639I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:46650943 C>A maps to NM_005727.3 T214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:46659045 C>A maps to ENST00000371986 V347V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:63069638 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:97700416 G>T maps to NM_000110.3 S811S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:110038446 C>A maps to NM_001134400.1 R108R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:113239250 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:120057075 C>A maps to ENST00000235547 T312T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:120283016 C>A maps to NM_006623.3 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:147141956 C>A maps to NM_016361.3 E72*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:150967097 C>A maps to NM_003568.2 R300R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:153736359 G>T maps to ENST00000428986 E608*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:154072548 C>A maps to NM_207308.2 L630L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:154544110 C>A maps to NM_000748.2 S271*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:155723184 G>A maps to ENST00000368331 Y1884Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:158576302 C>T maps to NM_001004478.1 L25L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:158735809 G>A maps to NM_001005185.1 I221I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:161762109 C>A maps to NM_007348.2 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:166819235 C>A maps to NM_017542.3 R474R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:180044160 C>T maps to NM_014810.4 L1858L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:181690901 G>T maps to ENST00000357570 T655T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:208205046 G>T maps to NM_025179.3 R1705R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:208207858 G>T maps to NM_025179.3 R1615R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:237551444 C>A maps to NM_001035.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:248112584 G>A maps to NM_001001963.1 L142L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:35300777 C>A maps to NM_001198778.1 E721*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:45472881 G>A maps to NM_007021.3 L199L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:61830132 G>A maps to NM_020987.2 F3502F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:61830688 G>C maps to NM_020987.2 S3317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:70451546 G>T maps to NM_030625.2 A2129A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:70856963 C>A maps to NM_002727.2 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:71648058 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:72360283 G>A maps to NM_005041.4 I125I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:99052374 C>A maps to NM_032900.4 E4*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr10:129160421 C>A maps to ENST00000398025 P1171P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:612737 C>A maps to NM_004031.2 L486L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:1276039 C>A maps to ENST00000447027 T5201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:4936272 G>A maps to NM_001005238.1 V207V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:6023702 C>A maps to NM_001005179.2 G226*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:6265395 C>A maps to NM_001037329.2 S495S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:6629395 C>A maps to NM_001014795.1 P70P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:9007341 G>T maps to NM_020645.2 R160R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:26734187 C>A maps to NM_178498.3 T135T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:57583416 G>T maps to NM_001085458.1 E947*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:61067643 G>T maps to NM_001923.3 L1129L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:66039909 G>T maps to NM_030981.2 V86V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:66291193 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:67352041 G>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:68197136 C>T maps to NM_002335.2 L1244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:71932251 G>T maps to NM_001113536.1 L124L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:76867816 C>A maps to NM_000260.3 P194P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:85963188 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:117097975 C>A maps to NM_004716.2 V222V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:117376367 C>A maps to NM_020693.2 S681S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:121031058 C>A maps to NM_005422.2 T1635T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:125647348 C>A maps to NM_212555.2 L90L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr11:126073515 C>A maps to NM_032795.2 E311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:2763020 C>A maps to NM_199460.2 L1413L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:6935829 C>A maps to NM_019858.1 R410R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:18435656 C>A maps to NM_004570.4 P214P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:27110592 C>A maps to NM_015633.2 R105R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:47160563 C>A maps to NM_018018.4 G522*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:49523318 G>T maps to NM_006082.2 R64R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:66522753 G>A maps to NM_032338.3 Q45*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:77236754 C>A maps to NM_015336.2 T441T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:96260963 C>A maps to NM_182496.2 G528*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:105428113 C>A maps to NM_001034173.3 V736V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:118293233 T>C maps to ENST00000339824 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:121648005 C>T maps to NM_002560.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr12:130184835 C>A maps to NM_133448.2 E163*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr13:29600790 C>A maps to NM_001033602.2 P662P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr13:33320180 C>A maps to ENST00000400481 P893P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr13:48986106 G>T maps to NM_005767.5 A151A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr13:52603704 G>C maps to NM_021645.5 V255V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr13:79945131 C>T maps to ENST00000438737 E195E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:23871958 C>A maps to NM_002471.3 G317*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:24775202 G>C maps to NM_014430.2 L159L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:31364870 C>A maps to NM_001083893.1 G741*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:36004981 C>A maps to NM_032594.3 P508P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:64727167 G>T maps to NM_001437.2 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:64882194 C>A maps to NM_005956.3 P120P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:73718793 C>A maps to ENST00000427855 P304P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:101200545 C>A maps to NM_003836.5 S155S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:102900644 C>A maps to NM_014844.3 P497P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:103412004 G>T maps to NM_006035.3 R1269R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:105207039 C>A maps to NM_199165.1 S236S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr14:105409721 G>A maps to NM_138420.2 S4022S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr15:39879560 G>T maps to NM_003246.2 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr15:41101604 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr15:49170897 C>A maps to NM_014335.2 T175T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr15:52575068 G>T maps to NM_018728.3 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr15:85186784 G>T maps to NM_032856.2 P351P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr15:86269659 C>G maps to NM_006738.4 L2259L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:700091 G>T maps to NM_145294.4 T68T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:2140728 C>A maps to NM_001009944.2 G4028G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:2482984 G>T maps to NM_001761.2 L65L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:5077983 C>A maps to NM_016256.3 E375*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:18826793 G>T maps to ENST00000389467 P3495P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:30616235 C>A maps to NM_138447.1 T284T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:30794181 G>T maps to NM_001080417.1 P489P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:46764574 G>T maps to NM_182493.2 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:48256670 G>T maps to NM_032583.3 L205L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:55359008 C>A maps to NM_024335.2 S2S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:56518731 G>A maps to NM_031885.3 R703*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:56667681 C>A maps to NM_176870.2 P38P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:57060303 C>A maps to NM_032206.3 P483P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:67337157 G>T maps to NM_001100915.1 P178P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:67473179 C>A maps to NM_004691.4 L212L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:70602965 C>A maps to NM_012426.4 T1062T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:81972428 C>A maps to NM_002661.2 P1074P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr16:83994322 C>A maps to NM_013370.3 P201P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:1551759 G>T maps to NM_031430.2 P235P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:4726140 C>A maps to NM_002663.3 P928P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:5485299 G>T maps to NM_033004.3 P177P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:6493253 G>T maps to NM_014804.2 A877A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:7323846 G>T maps to NM_199339.2 L48L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:7497258 C>A maps to NM_004860.3 E362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:8110899 G>T maps to NM_004217.2 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:8790469 G>T maps to NM_001142633.1 P616P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:18075033 C>A maps to ENST00000205890 R3389R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:39525978 G>T maps to ENST00000394004 P9P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:39887799 G>A maps to ENST00000310778 L338L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:40035062 C>A maps to ENST00000401700 G838*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:46239836 C>G maps to NM_003726.3 L324L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:72349698 G>T maps to NM_153209.3 E763*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:73504315 C>A maps to NM_020753.3 G49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:76487602 G>T maps to ENST00000389840 G2183G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:76510966 C>A maps to ENST00000389840 V1330V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:76970877 C>A maps to NM_005567.3 E90*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:77809185 G>T maps to NM_003655.2 T85T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:78120724 C>G maps to NM_014740.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:79803580 G>T maps to NM_000918.3 P405P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr18:5395092 C>A maps to NM_012307.2 T1042T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr18:22048830 C>T maps to NM_021624.3 L91L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr18:32455261 C>A maps to NM_001390.4 P574P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr18:34340686 C>A maps to NM_025135.2 P1339P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr18:43253768 C>A maps to NM_007163.3 L833L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr18:59221606 C>A maps to NM_031891.2 P695P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr18:60563127 C>A maps to NM_194449.2 P776P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr18:67727138 G>T maps to NM_173630.3 P1629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:618519 G>T maps to NM_005035.3 S1130S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:2438282 C>A maps to NM_032737.2 E168*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:4453968 G>T maps to NM_025241.2 R69R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:4552609 C>A maps to NM_032108.3 V271V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:5711979 G>T maps to NM_004793.2 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:9074986 C>A maps to NM_024690.2 V4153V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:13216373 G>T maps to NM_001136035.2 R544R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:44056371 C>A maps to NM_006297.2 G293G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:47725136 C>A maps to NM_001127240.1 E203*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:47885235 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:50902149 C>A maps to ENST00000391817 P14P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:51518765 G>T maps to NM_001077500.1 I195I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:54481482 C>A maps to NM_031895.5 R123R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:55450842 G>A maps to ENST00000446217 F476F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr19:55889357 G>T maps to NM_139172.1 R107R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:28772920 C>A maps to NM_153021.4 T351T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:32626578 C>T maps to NM_016252.3 Q436*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:47748460 G>T maps to NM_022055.1 S293*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:63826355 C>G maps to NM_005917.3 S143*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:79350316 C>A maps to NM_002909.4 S159S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:98349453 C>A maps to NM_001079.3 P224P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:113082226 C>A maps to NM_198581.2 P613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:160229598 G>T maps to NM_013450.2 P1390P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:162813737 C>A maps to NM_001178015.1 T927T. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HE-7130-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:203407088 C>A maps to NM_001204.6 P444P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:207041782 C>A maps to NM_005279.3 T63T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:208632221 C>A maps to NM_003468.3 V414V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:219540758 C>A maps to NM_015690.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:227907882 C>A maps to ENST00000396625 G1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:230675856 C>A maps to ENST00000389044 E684*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:234652391 C>A maps to NM_001001394.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:242607953 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr20:3211471 G>T maps to NM_001174090.1 A439A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr20:40033766 G>A maps to NM_032221.3 L2538L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr22:21140327 G>A maps to NM_000185.3 E400E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr22:26702083 G>A maps to NM_021115.4 E496E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr22:29957619 G>T maps to NM_003634.2 R152R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr22:32198756 C>A maps to NM_001136029.1 P338P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr22:37470715 C>A maps to ENST00000381792 G459*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr22:46931255 C>A maps to NM_014246.1 L604L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:10426997 C>A maps to NM_001001331.2 A318A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:15282099 C>A maps to NM_014296.2 R510R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:47452779 C>A maps to NM_015466.2 P1164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:48572989 C>A maps to NM_004567.2 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:50254717 C>A maps to NM_006841.4 T199T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:54930839 C>A maps to NM_018398.2 R771R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:62451041 G>T maps to ENST00000383709 T1217T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:101311469 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:121712499 C>A maps to ENST00000344209 E366*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:132402368 C>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:183454550 C>A maps to NM_018023.4 P286P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr3:196533523 C>A maps to NM_002577.4 P181P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:435552 G>T maps to NM_133474.2 T901T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:1643094 C>A maps to NM_001174070.1 G374G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:3021471 C>A maps to NM_182982.2 P282P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:47645250 C>A maps to NM_006587.2 L660L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:79440558 C>A maps to NM_025074.6 P3488P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:80246383 G>T maps to NM_032693.2 T216T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:85656206 C>A maps to NM_014991.4 E2328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:119161755 C>A maps to NM_004784.2 P732P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:129003390 C>A maps to NM_018078.2 R97R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:143326360 C>A maps to NM_003866.2 E85*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:156849515 G>T maps to NM_001334.2 A301A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:159789515 C>A maps to ENST00000379346 P599P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:186296880 C>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:187524810 C>A maps to ENST00000260147 T3626T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:223623 C>A maps to NM_004168.2 R31R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:66445361 G>T maps to NM_001164664.1 S1080S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:71495627 C>G maps to NM_005909.3 S2149*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:82786053 G>T maps to NM_004385.4 E70*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:125939611 C>A maps to NM_032177.3 S149S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:131819666 G>T maps to NM_002198.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:137727600 C>A maps to NM_016604.3 P760P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:139908296 C>A maps to ENST00000253810 P1922P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:140562427 C>A maps to NM_020957.1 P98P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:140588871 C>A maps to NM_018932.3 P131P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:140856909 G>A maps to NM_002588.2 L409L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:156186310 C>T maps to NM_000337.5 F261F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr5:171766566 G>T maps to NM_001017995.2 P514P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:7231013 G>T maps to NM_001003699.3 V894V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:29394923 G>T maps to NM_013937.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:29577061 C>A maps to NM_001470.2 L601L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:30573934 G>T maps to NM_002714.2 P240P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:30585699 C>A maps to NM_014046.3 R20R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:31112751 C>A maps to NM_001105564.1 E659*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:31324627 G>A maps to ENST00000428231 F60F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:35810320 G>T maps to ENST00000361690 R577R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:37622576 C>A maps to ENST00000297153 T237T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:39866676 G>T maps to ENST00000398904 V881V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:41874929 G>T maps to NM_004275.3 P173P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:43008725 G>A maps to NM_001168370.1 L1329L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:43034769 G>T maps to NM_201523.1 L294L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:43181267 T>C maps to ENST00000354495 P1817P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:43589883 C>A maps to NM_019096.3 P496P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:44227839 C>A maps to NM_004556.2 A459A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:46830807 G>T maps to NM_015234.4 P672P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:51914989 C>A maps to NM_138694.3 A748A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:54805491 G>T maps to NM_001010872.1 E575*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:55925754 G>T maps to NM_030820.3 P762P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:90499593 C>A maps to NM_014611.1 G379*. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HE-7130-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr6:149285590 C>A maps to NM_005715.2 P191P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:5348894 G>T maps to NM_001080495.2 G2831G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:6456385 C>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:43484554 C>A maps to NM_015052.3 S595*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:44807167 C>A maps to NM_031449.3 P903P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:56006984 C>A maps to NM_182633.1 P193P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:97846740 C>A maps to ENST00000379795 P1155P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:107718722 G>T maps to NM_007356.2 P642P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:117432364 C>A maps to NM_033427.2 V295V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:142561026 G>T maps to NM_004445.3 A14A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:143175819 C>T maps to NM_176883.2 F285F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:150720229 G>A maps to NM_173681.5 L241L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr7:150817096 C>A maps to NM_031946.4 A331A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr8:23429211 G>T maps to NM_016612.2 R287R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr8:26365434 C>A maps to NM_007257.5 A279A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr8:42587044 G>T maps to NM_000749.3 G199*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr8:77763548 C>A maps to NM_024721.4 P1464P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr8:99019719 C>T maps to ENST00000254898 C488C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr8:146017218 C>A maps to NM_000973.3 T73T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:15172107 C>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:34659808 C>A maps to NM_001142784.1 P288P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:35555517 C>A maps to NM_001135999.1 R826R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:35675533 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:74340618 C>A maps to NM_013390.2 G686*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:91616939 C>A maps to NM_005226.2 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:100971073 G>T maps to NM_018421.3 R676R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-HE-7130-01A-11D-1961-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:117108980 G>T maps to NM_030767.4 S1161*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:123783918 C>G maps to NM_001735.2 L390L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:124080759 C>A maps to NM_000177.4 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:131708394 C>A maps to NM_014908.3 L396L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:131772448 G>T maps to ENST00000372554 R234R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:131864708 G>T maps to NM_000755.3 P200P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:139902386 G>T maps to ENST00000355090 L2465L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr9:140331053 G>T maps to NM_001033113.1 S235S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:2343307 C>A maps to NM_145177.2 T49T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:26213114 C>A maps to NM_173523.2 P384P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:38178081 C>A maps to NM_001034853.1 E157*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:44870204 G>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:47516972 C>A maps to NM_153477.1 V94V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:71426808 G>C maps to NM_017669.2 S603*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:118370496 C>T maps to NM_006667.3 S57S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:119505018 C>A maps to NM_001142447.2 P172P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:123202455 C>T maps to NM_001042750.1 Q770*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:134991804 C>A maps to NM_018666.2 T530T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:153693837 C>A maps to NM_017514.3 P772P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:957702 C>A maps to NM_198576.2 S108S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:20233030 T>C maps to NM_015207.1 N314N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:156851383 C>T maps to NM_002529.3 L781L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr1:161495203 G>A maps to NM_002155.3 G252G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr10:122664156 G>A did not map to a codon.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr12:66546146 T>C maps to ENST00000286424 L119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr13:77460121 C>G maps to NM_138444.3 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr14:23524348 T>A maps to NM_022478.3 K139*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr14:104565245 C>T maps to NM_001080464.1 D190D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr16:30734927 T>C maps to NM_006662.2 L1395L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr16:56396895 A>G maps to NM_001144.4 S619S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr17:36508825 C>A maps to NM_014598.2 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr19:54648052 G>A maps to NM_014516.3 K156K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr2:242026824 A>T maps to NM_001080437.1 R1380R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr21:37408417 G>C maps to NM_017438.3 T440T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr22:21119516 C>T maps to NM_058004.2 W757*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr3:17550056 A>G maps to NM_001134381.1 Y2Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr3:101404667 T>C maps to NM_000986.3 G62G. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-HE-A5NF-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr4:100231923 T>C maps to NM_000668.4 K367K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr5:147661755 C>T maps to NM_001040129.2 H66H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NF-01A-11D-A26P-10 chr6:32119880 C>T did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr1:23693622 G>A maps to NM_001077195.1 T24T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr1:44595404 C>G maps to NM_173484.3 P154P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr12:6760400 C>T did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr12:29502994 A>T maps to NM_016570.2 I193I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr15:54557622 T>A maps to ENST00000260323 V1249V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr15:69072439 C>A maps to NM_006305.3 E244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr18:8378411 G>T maps to NM_001105244.1 R1204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr2:220349150 C>T maps to NM_005876.4 S2322S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr2:220470427 G>T maps to NM_052902.2 L250L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr20:60967981 C>G maps to NM_031215.2 S326S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr22:20077781 G>C did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr22:46931729 G>A maps to NM_014246.1 Y446Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr3:53126087 T>A did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr4:47427722 C>G maps to NM_000812.3 T371T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr6:25811998 C>T did not map to a codon.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr8:19811709 C>T maps to NM_000237.2 D207D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr8:62460749 C>T maps to NM_004318.3 E548E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr8:145745729 A>G maps to NM_014665.2 T146T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NH-01A-11D-A26P-10 chr9:131256868 T>C maps to NM_153435.1 A675A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:16260462 T>G maps to NM_015001.2 V2576V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:19611545 A>G maps to NM_012067.2 F190F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:21952820 G>T maps to NM_001145658.1 S50S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:35569919 G>C maps to NM_024772.3 V148V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr1:203819760 C>T maps to NM_014827.4 L686L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr10:32320042 A>G maps to NM_004521.2 T513T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr10:95549894 T>C maps to NM_005097.2 D157D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr12:53722358 C>T maps to NM_001173467.1 R289R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr15:70991968 G>A maps to NM_018003.2 R37*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr15:101865151 A>G maps to NM_002570.3 A759A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr16:58031773 G>A maps to NM_020807.1 F132F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:35615280 A>T maps to NM_198834.1 I505I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:39092458 C>G did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr17:65362548 G>C maps to NM_002816.3 P29P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr18:21914247 T>C maps to NM_080597.2 A147A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr18:29218693 G>A maps to NM_004775.3 R167R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:4511772 G>A maps to NM_001080400.1 V719V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:55805596 G>T maps to NM_032430.1 A197A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:58724016 G>C maps to NM_133502.1 R489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr19:59082639 G>A maps to NM_198055.1 G39G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:25972918 C>T maps to NM_018263.4 E502E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:74320720 G>T maps to ENST00000409262 G972G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:102493591 C>G maps to NM_145686.2 V1059V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr2:216271072 C>T maps to NM_212482.1 R958R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr20:8608960 T>G maps to NM_015192.2 L89L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr22:33679189 G>A maps to NM_133642.3 F625F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr3:53220040 A>T maps to NM_212539.1 K362*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr5:80037367 G>C did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:32169042 C>T maps to NM_004557.3 R1330R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:56501421 C>T maps to ENST00000361203 W787*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:89793800 T>C maps to NM_006813.2 P290P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:119245293 T>C did not map to a codon.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr6:167435949 C>A maps to NM_007045.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr7:73249147 A>C maps to NM_152559.2 S221S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr7:154862731 G>T maps to NM_024012.2 V41V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:19435059 C>T maps to NM_001010887.2 L161L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:97081336 C>A maps to NM_017561.1 G561*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:99700840 G>T maps to NM_001170741.1 G546*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:114332439 A>G maps to NM_001146108.1 F270F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chr9:131386740 G>A maps to NM_001130438.2 K1989K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chrX:39923131 G>T maps to NM_001123385.1 T1192T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NI-01A-11D-A26P-10 chrX:110654010 C>T maps to ENST00000358070 P55P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr12:72233487 T>A did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr12:110565895 C>T maps to NM_014055.3 R64*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr14:57960295 T>A maps to NM_018168.2 S46S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr15:41669494 C>T maps to NM_016359.3 Q409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr15:75499666 C>T maps to NM_015492.4 C426C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr16:84094305 G>C maps to NM_003791.2 V895V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr17:37373421 G>A maps to NM_198993.3 N134N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr17:73565070 C>A maps to NM_001031803.1 G445G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr19:2915554 C>T maps to NM_173480.2 F13F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr19:3543942 C>T maps to NM_001135580.1 L189L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr19:17322845 G>A maps to NM_004145.3 T2067T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr2:73836706 C>T maps to NM_015120.4 Q4158*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr2:230787147 T>G did not map to a codon.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr22:19709429 C>T maps to NM_002688.5 C300C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr22:30416248 C>T maps to NM_021090.3 C867C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:10263418 G>A maps to NM_012073.3 G497G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:71739708 C>T maps to NM_152625.1 R703R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:127477531 T>A maps to NM_001046.2 V544V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr5:149361288 T>C maps to NM_000112.3 S711S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr7:75183808 C>T maps to NM_005338.4 T660T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr7:80302112 A>T maps to NM_001127444.1 K385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NJ-01A-11D-A26P-10 chr9:97082578 G>A maps to NM_017561.1 Q427*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:78414968 A>G maps to ENST00000436586 A621A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:90179187 T>C maps to NM_032270.4 Y353Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:169446749 G>A maps to NM_006996.2 D150D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:181701627 G>A maps to ENST00000357570 A802A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr11:6789369 G>T maps to NM_001004490.1 I273I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr12:2763056 C>T maps to NM_199460.2 I1425I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr12:71002987 G>A maps to NM_001109754.1 T280T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr16:30666136 G>A maps to NM_024031.2 L282L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:56833489 G>A maps to NM_014906.3 E44E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:57746159 C>T maps to NM_004859.3 S717S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr17:61616009 C>G maps to NM_030779.2 V647V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr18:74680293 G>T maps to NM_007345.3 *1846L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr19:2210829 C>T maps to ENST00000221482 Q443*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr19:11594520 G>A maps to NM_138783.3 S608S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr19:19371724 G>A maps to NM_023002.2 S127S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr2:98907041 G>A maps to NM_144992.4 Q1038Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr2:179701994 A>T maps to NM_173648.3 A1317A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr20:16359621 G>A maps to NM_024704.4 L1009L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr20:37653977 C>T maps to NM_021931.3 Q593*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr20:48431565 T>C maps to ENST00000417961 H16H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:26422671 C>T maps to ENST00000407587 P2246P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:29885428 T>C maps to NM_021076.3 S600S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:38483171 G>T maps to NM_025045.4 S406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr22:40367066 C>T maps to NM_004810.2 Y324Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr4:164061508 T>C maps to NM_138386.2 A248A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr5:37121779 A>G maps to NM_023073.3 L2988L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr5:72864378 T>A maps to NM_032175.2 L106L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr6:35182248 C>T maps to ENST00000394681 A18A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr6:49936557 T>C maps to NM_001037729.1 E27E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr7:91631220 A>T maps to NM_005751.4 K664*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr7:150069171 C>A maps to NM_001099695.1 S338*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr8:1513949 C>T maps to ENST00000357934 D386D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr9:19126157 C>A maps to NM_001122.2 V60V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr9:133342186 G>C did not map to a codon.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chrX:50658964 C>T maps to NM_005448.2 N179N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr1:94486857 A>G maps to NM_000350.2 Y1652Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr1:159170697 G>T maps to NM_021189.3 E429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr10:117075178 G>A maps to NM_207303.2 E990E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr11:1264091 C>T maps to ENST00000447027 R1997R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr11:76891502 G>A maps to NM_000260.3 K890K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr11:124623586 C>T maps to NM_138961.2 V376V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:22291587 C>T maps to NM_013302.3 G653G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:27459982 G>T maps to NM_181079.4 T354T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:57503975 G>A maps to NM_032940.2 G181G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr16:87760466 C>T maps to NM_017566.3 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr17:47781477 T>A maps to ENST00000415270 T250T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr17:66526490 G>A maps to NM_212472.1 K349K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr2:44203319 T>A maps to NM_133259.3 A233A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr2:74642883 G>A maps to NM_001145054.1 P143P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr2:166152283 A>G did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:13868445 G>T maps to NM_025229.1 A238A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:33623073 A>C maps to NM_015638.2 L301L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:56140805 C>A maps to NM_002591.3 P605P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr20:62366739 T>A maps to NM_032527.4 P427P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr3:150877785 C>T maps to NM_053002.4 G335G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:39435930 G>T maps to NM_175737.3 R309R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:46043271 C>T did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:76570829 A>T maps to NM_203505.2 A411A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr4:126239107 T>C maps to NM_024582.4 I514I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr5:139876315 A>G maps to ENST00000253810 E819E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr5:154395500 G>A maps to NM_001099293.1 Q694Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr7:97847036 C>T maps to ENST00000379795 E1119E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chr8:113516206 C>G did not map to a codon.
Sequencing variant TCGA-HE-A5NL-01A-11D-A26P-10 chrX:34148835 C>T maps to NM_203408.3 E520E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr1:156209391 A>C maps to NM_007221.3 *206C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr10:103789496 C>T maps to NM_024541.2 L104L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr11:14536020 C>A maps to NM_148976.2 E97*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr12:125397654 C>A maps to NM_021009.5 L221L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr16:732018 G>T did not map to a codon.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr16:81094971 G>A maps to NM_152337.2 Q328*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr17:76449534 G>T maps to ENST00000389840 V3459V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr18:8314789 C>T maps to NM_001105244.1 R952*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr19:51584904 G>T maps to NM_022046.4 T48T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr2:206921630 G>A maps to NM_017759.4 I85I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr22:39814794 G>A maps to NM_006116.2 L203L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr3:140401753 G>A maps to NM_152616.4 K264K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40U-01A-11D-A25F-10 chr5:7816983 C>T maps to NM_020546.2 P963P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr1:90048544 A>G maps to NM_015350.2 K112K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr2:179615957 C>T maps to ENST00000375038 T3725T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr3:38519722 G>A maps to NM_001106.3 L154L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr4:140811101 C>T maps to ENST00000509479 Q496Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr5:1219217 C>T maps to NM_001003841.2 L458L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr6:5260905 T>A maps to NM_001164840.1 K21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr7:5396873 G>A maps to NM_001080495.2 Q1623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chr7:156742604 A>G maps to NM_138400.1 E58E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40X-01A-11D-A25F-10 chrX:7811789 C>T maps to NM_013452.2 S118S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr1:155726781 C>T maps to ENST00000368331 R1828R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr1:161989777 C>G maps to ENST00000451379 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr1:222715412 G>A maps to NM_024746.3 F353F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr11:18738380 A>G maps to NM_173588.3 D380D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr12:132522574 G>A maps to ENST00000333577 V2083V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr13:50134122 G>C maps to NM_018191.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr13:101881860 T>C maps to NM_052867.2 G503G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr14:64519116 T>G maps to NM_182914.2 L2829*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr16:29982730 G>A maps to NM_194280.3 E196E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr17:7689596 C>T maps to NM_020877.2 R2095R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr17:10300167 A>T maps to NM_002472.2 S1438S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr19:15587342 G>T maps to NM_052890.3 T46T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:44566371 G>A maps to NM_001171603.1 R295*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:44566450 A>G maps to NM_001171603.1 N268N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr2:234368473 C>T maps to NM_152879.2 V922V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr22:31484746 G>C maps to ENST00000454496 R173R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr3:10089632 G>A maps to NM_033084.3 S437S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr3:151475279 T>C maps to NM_207365.3 D368D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr4:54244013 C>T maps to NM_030917.3 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr5:101811426 G>A maps to NM_173488.3 V291V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr5:180050942 T>A maps to NM_182925.4 K514*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr6:51889789 G>A maps to NM_138694.3 V1606V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr6:89859123 T>A maps to NM_001010853.1 A202A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chr9:116153878 C>T maps to ENST00000277315 E72E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IA-A40Y-01A-11D-A25F-10 chrX:150889895 G>A maps to NM_033085.2 L88L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr1:15987647 T>C maps to NM_006511.1 L429L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr1:109792761 T>C maps to NM_001408.2 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr10:103563516 A>G maps to NM_012215.3 N337N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IZ-8195-01A-31D-2396-08. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr11:76903187 C>T maps to NM_000260.3 N1339N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr11:129817184 G>A maps to NM_020228.2 T125T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr13:20398976 A>G maps to NM_001142684.1 F550F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr13:109793008 C>T maps to NM_015011.1 H1461H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:35085734 G>A maps to NM_005159.4 Y55Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:57808994 G>T maps to NM_032866.3 A807A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:77759507 C>A maps to NM_018200.2 P103P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr16:2258564 C>T maps to NM_022372.4 G271G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr17:3550807 C>T maps to NM_001031681.2 L44L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr19:42814765 C>T maps to NM_199285.2 P315P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr19:46394099 C>T maps to NM_001012643.2 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:54080606 A>G maps to NM_006794.2 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:85875074 T>G maps to NM_006590.2 L529*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:149248039 A>C maps to ENST00000404807 P1613P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr2:223066672 C>T maps to NM_181459.3 Q470Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr3:38180514 C>T maps to NM_001172567.1 S121S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr4:3519767 A>G maps to NM_002337.2 T248T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr4:140811107 C>T maps to ENST00000509479 Q494Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:80040401 G>A maps to NM_002439.3 K577K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:177580731 G>T maps to NM_017838.3 V29V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:179193184 G>T maps to NM_014757.4 E392*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr6:135644422 C>A maps to NM_017651.4 E1069*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr7:48411808 C>A maps to NM_152701.3 A3616A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr8:61192347 C>T maps to NM_004056.4 S64S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr9:139273026 C>G maps to NM_003086.2 G1084G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:15956838 C>T maps to NM_032341.4 F96F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:20416293 G>A maps to NM_000929.2 A66A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:110882977 T>C maps to NM_022768.4 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:154314971 C>T maps to NM_020452.3 V453V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:205028741 C>A maps to NM_005076.3 A243A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr10:103917062 A>G maps to ENST00000405356 Q98Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr11:82877726 A>G maps to NM_015885.3 R596R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr13:47354150 A>G maps to NM_001984.1 A173A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr14:20666033 C>T maps to NM_001005503.1 T180T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr15:84592740 T>C maps to NM_207517.2 P691P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr16:26147415 G>A maps to NM_006040.2 P406P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr16:61851549 C>T maps to NM_001796.2 G370G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr16:66857504 T>C did not map to a codon.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:12016634 T>C maps to ENST00000415385 S268S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:40695934 C>T maps to NM_000263.3 F637F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:42117588 C>T maps to ENST00000411445 K101K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr17:58156269 A>G maps to NM_022070.4 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr19:2255342 G>A did not map to a codon.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr19:47856880 C>G maps to NM_014681.5 Y198*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:11960559 A>G maps to ENST00000396099 V853V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:84777108 A>T maps to NM_001370.1 L471L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr2:228860229 G>C maps to NM_001142644.1 S1543S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr20:60982023 C>T maps to NM_031215.2 L103L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr21:47421873 G>A did not map to a codon.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr22:51018474 A>C maps to NM_005198.4 V285V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr3:184019769 C>T maps to NM_002808.3 C205C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr4:46312217 A>T maps to ENST00000507069 A177A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr4:89408217 A>G did not map to a codon.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:122359695 T>A maps to NM_000943.4 T171T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:140223200 G>A maps to NM_018911.2 P765P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr5:140811804 G>A maps to NM_003735.2 E493E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr6:30640453 G>T maps to NM_003587.4 L55L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr7:19738031 C>T maps to NM_001002926.1 K308K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr7:31877506 C>T maps to NM_001191057.1 K353K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr8:94747483 A>G maps to NM_203390.2 H385H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr8:145540218 A>T maps to NM_012079.4 *489R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:2418422 G>A maps to NM_014638.2 G298G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:7854050 T>C maps to ENST00000377532 P209P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:10713662 G>A maps to NM_001079843.1 T817T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:10714627 G>A maps to NM_001079843.1 Y562Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:23380288 G>A maps to NM_001009999.2 L249L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr1:200378263 C>T maps to NM_012482.3 Q190Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr10:113913351 G>A maps to NM_020918.4 R815*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr11:8639492 A>G maps to ENST00000402157 *1246R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr13:20413048 G>T maps to NM_001142684.1 A221A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr14:20774051 T>C maps to NM_138376.2 K15K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr14:75019016 C>G maps to NM_000428.2 G424G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr15:30019081 T>G maps to NM_003257.3 T738T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr15:77750832 C>G maps to NM_018200.2 T28T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr15:78758792 A>T maps to NM_004136.2 T197T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr16:70605580 G>A maps to NM_012426.4 V1173V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr17:27948313 G>A maps to ENST00000345068 V113V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr17:80047602 C>G did not map to a codon.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr19:11019855 G>A maps to NM_199141.1 L177L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr2:39284008 T>C did not map to a codon.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr2:239186361 C>T maps to NM_022817.2 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr20:20033151 G>A maps to NM_016652.4 A106A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr20:30730876 C>T maps to NM_014742.3 F207F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr3:57136552 C>T maps to NM_017563.3 S311S. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-IZ-A6M8-01A-11D-A31X-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr4:135121147 C>A maps to NM_001114734.1 E401*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr4:144445523 C>T maps to NM_003601.2 R142*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr5:118479555 T>C maps to NM_005509.4 F799F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr5:126705694 G>T did not map to a codon.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr7:4056808 C>T maps to NM_152744.3 R809R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr7:40134338 T>C maps to NM_003718.4 P1433P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr8:23294704 G>A maps to NM_004901.3 D372D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr8:49647694 G>A maps to NM_024593.3 L6L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:441957 C>T maps to NM_203447.3 V1813V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:71628288 G>A maps to NM_002732.3 Y240Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:74838061 A>G maps to ENST00000238018 T211T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:130982345 G>A maps to ENST00000372923 K223K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr9:139748711 C>T maps to ENST00000392881 V240V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:9809528 G>A maps to NM_001009566.1 H325H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:152128053 T>C maps to NM_001122965.1 Q507Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:202701001 A>C maps to ENST00000367264 Y1361*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr10:5855179 C>A maps to NM_001494.3 L14L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr11:1092629 T>C maps to ENST00000441003 T1483T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr13:72440445 G>A maps to ENST00000359684 S154S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr15:42143072 G>A maps to ENST00000320955 R3634*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:707222 T>G did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:67913802 C>T maps to NM_014329.3 S624S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:75678299 A>T maps to NM_001130089.1 L9L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr16:89345818 G>A maps to NM_013275.4 D2377D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr17:27014485 G>T maps to NM_003170.3 L1001L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr17:37341118 T>A did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr19:2410352 G>A maps to NM_182973.1 V371V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr19:8503276 C>T maps to NM_016496.4 S196S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr19:40331278 G>A maps to NM_001436.3 G53G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr2:152382498 G>A maps to NM_001164507.1 V7378V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr2:189867766 C>T maps to NM_000090.3 P844P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr22:42910735 C>T maps to NM_015703.4 R170R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr3:52731771 G>T maps to NM_018446.2 Y98*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr4:54343068 T>C maps to NM_001126328.1 T581T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr6:153293426 G>A maps to NM_012177.3 R358*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr6:170871003 G>A maps to NM_003194.4 Q60Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr7:70255843 A>G maps to NM_015570.2 T1214T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr7:135307640 C>T maps to NM_015135.2 R1483*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chrX:54841946 C>T maps to NM_201222.1 A551A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chrX:117786021 T>C maps to ENST00000276204 N1559N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr10:99531062 T>C maps to NM_003015.3 P176P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:21769355 C>G maps to NM_020366.3 L150L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:23549775 T>C maps to NM_014977.3 V314V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:24793366 C>A maps to NM_139247.3 L649L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr14:59965573 T>C maps to ENST00000356057 L210L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr16:74640707 A>C maps to NM_012201.5 G95G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr19:5622657 C>A maps to NM_014649.2 A23A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr19:43585216 A>T maps to ENST00000449000 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr2:230875428 A>G maps to NM_174899.4 K132K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr21:47542787 G>A did not map to a codon.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr3:172025191 C>G maps to NM_022763.3 S367S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr4:170028337 A>G maps to NM_020870.3 L720L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:16877716 C>G did not map to a codon.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:121413455 G>C maps to NM_002317.5 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:130500844 G>T maps to NM_005340.5 I18I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr5:179326224 C>T maps to NM_198868.2 E104E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr8:75227664 G>A maps to NM_020647.2 R190R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr8:143956728 C>G did not map to a codon.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:3334450 C>T maps to NM_022114.3 D917D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:36642064 G>A maps to NM_018067.3 P372P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:94009755 G>A maps to ENST00000370253 Q414Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr10:17495607 C>T maps to NM_001004470.1 A50A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr10:124361508 T>C maps to ENST00000368915 G1180G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr14:35269497 T>A maps to NM_013448.2 K354*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr16:19051690 C>A maps to NM_024847.3 I420I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr17:38187789 C>G did not map to a codon.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr17:45669356 A>T maps to NM_006310.3 I432I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr2:86832537 A>C maps to NM_005667.3 Y162*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr2:141607701 G>A maps to NM_018557.2 N1636N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr20:37555363 G>A maps to NM_030919.2 S123S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr4:104117118 A>C maps to NM_001813.2 V105V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr6:29797252 G>A maps to ENST00000376828 R231R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chrX:144904237 C>T maps to NM_001144010.2 Q99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:26873741 G>A maps to NM_001006665.1 L105L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:33625314 C>T maps to NM_018207.2 L245L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:38463362 G>T maps to NM_004468.3 P227P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr1:186316561 A>G maps to NM_003292.2 D935D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:6191109 G>A maps to NM_001004052.1 A149A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:57100281 C>A maps to NM_003146.2 T195T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:71948602 A>G maps to NM_001567.3 P1105P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:95825406 C>T maps to NM_032427.1 Q596Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:102100554 G>T maps to NM_001130145.2 G467*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr11:128933814 A>G maps to NM_001142685.1 P275P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr12:7302197 T>C maps to NM_014718.3 D718D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr14:99929880 C>T maps to NM_032233.2 E46E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr15:51828387 T>G maps to NM_001174116.1 P763P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr15:75705129 G>A maps to NM_001145357.1 Q244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr16:31373394 G>A did not map to a codon.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr19:34895340 G>T maps to NM_032346.1 A2A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr19:38948846 C>G maps to NM_000540.2 Y694*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr19:56487642 C>T maps to NM_176811.2 N950N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:85361149 C>G maps to NM_031283.2 R87R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:110873285 G>A maps to NM_005434.4 F28F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:238494740 C>A maps to NM_022449.3 V19V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr2:242173342 G>A maps to NM_005336.3 D1060D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr20:37383624 T>C maps to NM_024855.3 D267D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr20:47361657 G>A maps to NM_020820.3 I106I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr3:14508106 A>G maps to NM_001134367.1 A272A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr5:137088930 G>A maps to NM_006805.3 G275G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr5:177649896 T>C maps to NM_153373.2 G219G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GD-01A-11D-A31X-10 chr7:143049048 G>A maps to NM_000083.2 L986L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr11:6592936 G>T maps to NM_144666.2 A4661A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr11:66008915 T>A maps to NM_018026.2 Y816*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr11:67135056 G>T maps to NM_013246.2 L19L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:7528455 T>A maps to ENST00000416109 I852I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:52913573 G>T maps to NM_000424.3 R169R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:95867963 T>G maps to NM_006838.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr12:118506350 C>T maps to NM_019086.5 E466E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr15:62219325 A>G maps to NM_020821.2 P2160P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr15:72552950 G>T maps to NM_020214.2 L208L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr15:73884464 G>A maps to NM_012428.3 V151V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr16:68386312 G>A did not map to a codon.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr17:42399918 C>T maps to NM_001143780.1 L64L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr19:9088826 T>C maps to NM_024690.2 V996V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr19:54822786 A>C maps to NM_021250.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr19:58385872 T>C maps to NM_001144989.1 K295K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr20:32873356 G>T maps to NM_000687.2 G352G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr21:45502875 G>A maps to NM_003274.4 W644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr3:129281630 A>G maps to NM_015103.2 L1608L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr5:94957232 A>C maps to NM_199243.1 P418P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr6:37622224 G>T maps to ENST00000297153 P269P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr6:99894084 T>C maps to NM_001080481.1 R521R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr7:99686961 T>C maps to NM_006833.4 A42A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-KV-A6GE-01A-11D-A31X-10 chr7:148800799 A>G maps to NM_001001661.2 P721P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:39880151 A>T maps to NM_015038.1 V1405V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:65775556 C>T maps to ENST00000371069 A43A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:152059686 C>T maps to NM_001008536.1 V157V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:154744542 C>T maps to NM_002249.4 K452K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:205588956 C>G maps to NM_021795.2 *406S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr11:63671475 C>G maps to NM_001039469.2 S511S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr12:275006 G>A maps to NM_001170738.1 L974L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr12:7527335 G>T maps to ENST00000416109 R1047R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr14:91681815 C>T maps to NM_001102368.1 H544H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr14:105406109 A>C maps to NM_138420.2 G5226G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr15:42057123 C>T maps to ENST00000219905 N2644N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr15:59139572 A>T maps to NM_001040450.1 V482V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr17:46103805 C>G maps to NM_016429.2 S205S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr17:79518168 A>G maps to NM_025161.5 P117P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr18:29116285 T>C maps to NM_001943.3 V515V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr19:7964009 T>G maps to NM_025061.3 G201G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr19:12502159 G>T maps to NM_001080821.2 S351*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr2:24469666 A>G maps to NM_006277.2 P1128P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr20:46254224 G>A maps to NM_181659.2 Q119Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr21:15561569 G>A maps to NM_198996.2 Q94*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr22:17566095 C>A maps to NM_014339.5 R39R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr3:50155813 T>A maps to NM_005778.2 Y791*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr4:8607800 G>C maps to NM_001014447.2 L265L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr4:26585818 T>C maps to NM_018317.2 L2L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr4:141600811 G>A maps to NM_015130.2 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:38418271 C>A maps to ENST00000354891 G533G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:39383199 A>G maps to NM_001343.2 F287F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:89979467 T>C maps to NM_032119.3 D1910D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr5:171471933 T>G maps to NM_005990.3 P953P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr6:90459293 G>A maps to NM_014611.1 Q1195*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr7:56046041 G>C did not map to a codon.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr7:135370356 C>A maps to NM_012450.2 L506L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr7:151921113 A>T maps to ENST00000355193 C1103*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr9:131021445 C>T maps to NM_004486.4 Q672Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr9:132593304 G>T maps to NM_016520.2 I129I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chrX:73811994 G>T maps to NM_183353.2 P385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chrX:152938462 C>G did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:35223632 C>T maps to NM_005268.2 T234T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:228469851 G>T maps to NM_001098623.1 E2806*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr1:235884163 G>A maps to NM_000081.2 L3119L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr10:99116858 G>A maps to NM_015179.3 R1296*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr10:116100455 G>A maps to NM_001001936.1 F17F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr11:65319016 A>T did not map to a codon.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr11:129747270 G>A maps to NM_006165.3 D532D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:56862410 C>T maps to NM_207344.3 C12C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:101588896 C>T maps to NM_145913.3 V171V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr12:107713244 G>A maps to NM_001018072.1 A176A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr14:42360767 C>T maps to NM_152447.3 S567S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr14:75558058 G>A maps to NM_033116.4 R786*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr15:31251263 G>C maps to NM_017762.2 S273S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr15:51294807 T>G maps to NM_007347.3 T1121T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr16:4164713 G>A maps to NM_001116.3 L244L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr17:11998977 C>T maps to ENST00000415385 Y171Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr18:21508089 T>C maps to ENST00000416669 F2729F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:25469541 C>T maps to NM_175629.1 W409*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:39008787 C>T maps to NM_024775.9 F86F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:54482520 G>A maps to NM_001003937.2 F256F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:71607374 T>C maps to NM_014497.3 T763T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:74643026 G>T maps to NM_001145054.1 R96R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:217541548 C>G maps to NM_000599.3 G248G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:233633227 A>T maps to NM_002242.4 P252P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr2:233659497 T>A maps to ENST00000373566 P463P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr20:57282246 A>C maps to NM_024663.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr21:45107949 C>G maps to NM_015056.2 P565P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr3:197408101 G>A maps to NM_014687.1 F776F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr4:162307105 T>A maps to NM_020116.3 I779I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr4:186382295 A>G maps to NM_152775.3 S85S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr5:72183031 T>G maps to NM_002270.3 L429*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr5:150911352 G>A maps to NM_001447.2 G3202G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr5:178553060 G>T maps to NM_014244.4 A896A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr6:33172820 C>T maps to NM_014234.3 P65P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr7:30094388 T>C maps to ENST00000440706 T313T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55Z-01A-11D-A26P-10 chr8:144902838 T>C maps to NM_078480.1 Q115Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:153740252 G>T maps to ENST00000428986 E733*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:196654323 A>G maps to NM_000186.3 A307A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:198678921 C>T maps to ENST00000271610 N380N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:202097356 C>T maps to NM_004767.3 L373L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:214815374 G>T maps to NM_016343.3 E1232*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr1:243419489 G>A maps to NM_006642.3 P5P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr10:100481442 C>T maps to NM_021828.4 P309P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr10:124800166 G>A maps to NM_001609.3 L163L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr10:135439106 C>T maps to ENST00000443774 G112G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr12:6976717 C>T maps to NM_001159287.1 L33L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr14:60921716 A>T did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr17:29162088 T>A maps to NM_024857.3 P330P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr18:28598132 C>T maps to NM_001941.3 W389*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr19:44739324 A>T maps to NM_182490.1 K248*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr4:155526042 T>C maps to ENST00000407946 R443R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr6:32052211 C>T maps to ENST00000375244 P1141P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:11675887 G>A maps to ENST00000423059 R297R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:111161446 G>A maps to NM_032549.2 F19F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr7:141365047 A>T maps to NM_001080392.1 P297P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:8655001 C>A did not map to a codon.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:26365720 C>T maps to NM_007257.5 W184*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:38871522 C>T maps to NM_003816.2 N98N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A560-01A-11D-A26P-10 chr8:144522451 G>T maps to NM_015117.2 P858P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:6610593 G>A maps to NM_024654.4 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:26646660 G>T did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:36564105 A>G maps to NM_005202.2 I392I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:46124747 A>G maps to NM_021639.4 H4H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:48999846 A>G maps to NM_032785.3 *504Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:175996825 T>C did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr1:204101335 C>T maps to NM_018208.2 A379A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr11:94231478 C>T maps to NM_017704.2 I167I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr12:51758020 G>C maps to NM_007210.3 P311P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr15:93016233 T>C maps to NM_153040.2 D142D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:23360138 C>G maps to ENST00000307331 T118T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:70301661 G>A maps to ENST00000418685 I382I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:71127827 G>A maps to NM_032821.2 I446I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr16:84797743 G>A maps to NM_005153.2 Q569Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr17:42449791 C>T did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr17:49067111 G>T maps to ENST00000376407 V914V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr19:4433328 G>A maps to NM_005483.2 P822P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:69757188 G>A maps to NM_014911.3 F274F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:74668861 G>T maps to NM_001015055.1 R28R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:136555629 T>G maps to NM_002299.2 R1649R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:170136008 T>A maps to NM_004525.2 K480*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr2:239006932 C>T maps to NM_016510.4 A425A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr20:44539885 C>T maps to NM_006227.2 K35K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr21:45825793 C>T maps to ENST00000397932 I888I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr3:48488464 C>T maps to NM_130384.1 S72S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr3:49760822 A>C did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:34825519 C>T maps to NM_017754.3 Y531Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:75861880 T>C maps to ENST00000322507 A1267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:114264644 A>C maps to ENST00000398283 A510A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr7:124405026 G>A maps to NM_005302.2 R2*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr9:130707095 G>A maps to NM_001035254.2 I333I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chrX:53440301 C>G maps to NM_006306.2 A165A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chrX:102973933 T>A maps to NM_001172285.1 P328P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr1:40724032 G>C maps to NM_005857.3 V30V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr1:154920115 A>C did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr1:229771820 G>A maps to NM_014777.2 Q487Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr10:33543117 G>A maps to NM_003873.5 F273F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr11:43350299 A>T maps to NM_001142930.1 G328G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr11:64428552 A>T maps to NM_015080.3 I619I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr11:119185944 C>T maps to NM_006500.2 A32A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr15:65942808 A>G maps to NM_004727.2 G774G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr16:27374133 G>A maps to NM_000418.2 T487T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr16:89760631 C>T maps to NM_052988.4 I220I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr17:20355184 G>A maps to ENST00000324290 F228F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr17:62045581 C>T maps to NM_000334.4 K279K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr17:62045584 C>T maps to NM_000334.4 Q278Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:15651479 C>T maps to NM_173483.3 A297A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:19338432 A>C maps to NM_004386.2 P668P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:39226165 G>T maps to NM_144691.3 I534I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:43689068 C>A maps to ENST00000270059 E99*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr19:54721051 G>T maps to NM_001081450.1 T603T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-MH-A562-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr20:30253880 A>G maps to NM_138578.1 F191F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr3:49158998 C>T maps to NM_002292.3 Q1709Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr3:195509321 G>A maps to NM_018406.5 V3043V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr4:982689 A>G maps to NM_213613.2 S679S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr4:49032878 T>G maps to NM_025087.2 S470S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr4:82061796 A>T maps to NM_006259.1 A478A. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-MH-A562-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Multiple mappings detected for codon TCGA-MH-A562-01A-11D-A26P-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr5:82815684 G>A maps to NM_004385.4 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr5:180338540 C>T maps to NM_001040462.2 N200N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr7:45148885 C>T did not map to a codon.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr7:50742287 G>A maps to NM_005311.4 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr8:2832126 T>C maps to NM_033225.5 P2862P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr8:77616433 G>A maps to NM_024721.4 G37G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr9:5457409 G>A maps to NM_014143.3 V128V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A562-01A-11D-A26P-10 chr9:70177821 T>C maps to NM_001126334.1 S54S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:22073614 A>G maps to NM_032236.5 N312N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:40839875 T>A maps to NM_022733.2 C28*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:44083551 C>T maps to NM_002840.3 V1447V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:107599741 C>T maps to NM_018137.2 V135V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:153907293 C>T maps to NM_014856.2 Q905Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:155903552 C>G maps to NM_014949.2 G42G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:214813547 A>T maps to NM_016343.3 K623*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:223567035 C>T maps to NM_152610.2 R73R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:247588674 C>T maps to NM_004895.4 Q644*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr1:248309354 G>A maps to NM_001004690.1 R302R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:17278344 T>G maps to NM_003380.3 L442L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:81037037 C>G maps to NM_020338.3 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:90342857 A>C maps to NM_001031709.2 L30L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:96121494 T>C maps to NM_022451.9 K48K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr10:119134717 G>T maps to NM_173791.3 I7I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr11:58346867 G>A maps to NM_053023.4 A38A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr12:56865333 A>G maps to NM_013267.2 S582S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr14:23898981 A>G did not map to a codon.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr14:68268850 G>T maps to NM_015346.3 L528L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr15:31818595 G>A maps to ENST00000382902 S283S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr15:45427437 A>G maps to NM_175940.1 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr16:707786 C>T maps to NM_145294.4 P833P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr16:4432671 T>C maps to NM_138440.2 C598C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr16:31475858 C>T maps to ENST00000408912 R600R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr19:48183659 G>A maps to NM_015711.3 L411L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr19:48183986 G>T maps to NM_015711.3 L520L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:171572791 G>A maps to NM_001003845.2 P25P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:202900341 C>G maps to NM_003507.1 Y324*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr2:203500480 A>C maps to NM_173511.3 R191R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr3:50685440 C>G maps to NM_004635.3 G371G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr3:65425596 C>T maps to NM_001033057.1 Q409Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr6:30459404 T>C maps to NM_005516.5 A326A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E6-01A-11D-A28G-10 chr9:139794875 C>G maps to ENST00000359662 A90A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr1:24151845 A>G maps to NM_000191.2 A20A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr1:162729663 G>A maps to NM_006182.2 V250V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr10:7214000 G>A maps to NM_001018039.1 P757P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr10:134218415 C>T maps to NM_138499.3 L138L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr12:31551283 C>T maps to NM_144973.3 G1027G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr12:68696604 T>A maps to NM_017440.4 I589I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr14:24734892 C>T maps to NM_182836.1 P544P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr14:36143778 A>C maps to NM_194301.2 P1081P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:7127678 T>C maps to ENST00000356839 L570L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:7404999 G>A maps to NM_000937.4 K767K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr17:72942795 G>A maps to NM_178233.1 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr19:17767188 G>T maps to ENST00000428389 R350R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:33002959 G>A maps to NM_017735.4 W564*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:33813425 T>C maps to ENST00000395190 Q166Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:69409662 T>G maps to NM_032208.2 A408A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:74718486 G>A maps to NM_022492.4 Q223Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:84652538 C>T maps to NM_003849.3 K338K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:95976176 C>T maps to NM_013434.4 I30I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:108604762 T>A maps to NM_021815.2 L51*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:218678510 C>G maps to NM_022648.4 P1482P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:220164915 A>G maps to NM_002846.3 P409P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr2:241465101 C>T maps to ENST00000401804 Q445Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr20:10653489 A>C maps to NM_000214.2 Y82*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr20:33622950 G>T maps to NM_015638.2 A342A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:24106286 G>A maps to NM_182520.2 V13V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:30685453 C>T maps to NM_001037666.2 R11R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr22:39066950 G>A maps to NM_015373.3 L47L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr3:121415216 G>A maps to ENST00000393667 Q1385*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr3:137982981 C>T maps to ENST00000469044 H409H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr3:189711952 A>G maps to NM_018192.3 C251C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr5:102611691 C>T maps to NM_033211.2 N24N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr7:101882762 G>A maps to ENST00000360264 A1273A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E7-01A-31D-A28G-10 chr9:27950498 G>A maps to NM_152570.1 I57I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr1:154938021 A>C maps to NM_001130040.1 G541G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr1:179815211 A>C maps to NM_145034.4 L469L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr15:43748236 G>A maps to NM_001141980.1 Q857*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr16:4432542 A>C maps to NM_138440.2 T555T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr16:67683207 C>T maps to NM_001013838.1 D580D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr17:27437603 G>T maps to NM_078471.3 G979G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr17:45925060 G>A maps to NM_199262.2 P245P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr17:72306226 G>T maps to NM_023036.4 L473L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr2:44429129 A>G maps to NM_002706.4 V264V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr20:37570603 G>A maps to NM_030919.2 V192V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr4:123664663 T>C maps to NM_152618.2 G539G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr6:142396952 G>A maps to NM_002511.2 F335F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr6:168377104 G>A maps to NM_001129895.1 V76V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr7:15725799 G>A maps to NM_005924.4 H76H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr7:99972036 C>T maps to NM_013439.2 T145T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr7:104750954 G>T maps to NM_182931.2 P1292P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr1:84663464 T>C maps to NM_182948.2 C247C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr1:151552138 A>G maps to NM_020127.2 K313K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr11:2466534 G>T maps to NM_000218.2 A69A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr12:120572148 G>C maps to NM_006836.1 A2421A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr13:31036767 C>T maps to NM_002128.4 A126A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr16:3817822 C>A maps to NM_004380.2 E1050*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr16:30744760 A>G maps to NM_006662.2 E2096E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr18:19995947 G>C maps to NM_172241.2 L609L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr18:70532933 T>C did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:1003373 G>A maps to NM_138690.1 A224A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:9058715 G>C maps to NM_024690.2 S9577*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:22271295 G>A maps to NM_033468.2 K248K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr19:58384711 A>G maps to NM_001144989.1 H682H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr2:73675808 A>T maps to NM_015120.4 R718*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr2:170557974 T>A maps to NM_001008489.3 L165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr20:13561620 C>T maps to NM_017714.2 K137K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr22:30057328 G>A did not map to a codon.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:9959172 C>T maps to NM_153461.2 S58S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:78685207 G>A maps to NM_002941.3 L1030L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:119642254 G>T maps to NM_002093.3 R148R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr3:147128793 G>T maps to NM_003412.3 E299*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr4:42077745 T>C maps to NM_006345.3 D497D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr4:166996129 T>C maps to ENST00000507499 H786H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr6:31625013 C>G maps to NM_019101.2 L94L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr7:2956955 G>A maps to NM_032415.4 R891*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr7:70231265 G>A maps to NM_015570.2 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chr9:133914284 G>A maps to ENST00000355048 T337T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chrX:41022127 T>C maps to NM_001039590.2 L661L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chrX:48888985 G>A maps to ENST00000336239 Q404*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chrX:50144041 T>C maps to NM_001013742.1 K468K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chrX:57618714 C>T maps to NM_007157.3 T78T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EA-01A-11D-A28G-10 chrX:120182479 A>G maps to NM_012084.3 L314L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:12711236 G>T maps to NM_001013630.1 V88V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:25628089 G>A maps to ENST00000357542 V238V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:205306598 G>T maps to NM_018203.1 C327*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:243800912 C>T maps to NM_005465.3 K187K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr1:247694871 T>A maps to NM_198074.4 A314A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr10:13160993 C>T maps to NM_021980.4 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr11:14063069 C>T maps to NM_006108.2 I116I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr11:46799003 G>C maps to ENST00000415402 V949V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr11:47837536 A>G maps to NM_015231.1 S492S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:12483848 G>T maps to NM_018050.2 P136P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:14943405 A>G maps to NM_016312.2 P431P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:54756648 G>A maps to NM_020370.2 A329A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:57674167 T>C maps to ENST00000438036 P457P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:58165806 G>A maps to ENST00000408972 Y45Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:99093183 A>C did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:109290783 G>T maps to NM_001917.4 V205V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr12:113901231 T>C maps to NM_022363.2 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr13:36383186 A>G maps to NM_004734.4 Y578Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr14:21769307 C>T maps to NM_020366.3 A134A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr14:23828917 G>A maps to NM_005864.2 L257L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr14:105833602 C>T maps to ENST00000458164 I159I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:45048564 G>C did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:48748936 G>T maps to NM_000138.4 I1773I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:65494240 C>A maps to NM_003613.3 V385V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr15:65917017 C>A maps to NM_004727.2 Y200*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:683831 C>A maps to NM_053284.2 G474G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:1995883 C>T maps to NM_005061.2 L333L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:3779017 C>T maps to NM_004380.2 G2010G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr16:23713535 C>T maps to NM_033266.3 L428L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr18:42533243 C>T maps to NM_015559.2 D1313D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:10610177 G>A maps to NM_203500.1 Q178*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:15353720 G>T maps to NM_058243.2 P1053P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:33793107 G>T maps to NM_004364.3 A71A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:33793119 G>T maps to NM_004364.3 Y67*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:35758027 C>A maps to NM_205834.2 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:36279063 C>T maps to ENST00000007510 P1199P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr19:50412995 C>T maps to NM_012346.4 T23T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr2:170677783 C>A did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr21:15554118 C>T maps to NM_198996.2 T222T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:58242369 A>T maps to NM_020676.5 P19P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:122436992 C>G maps to NM_017554.2 S1359*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr3:171395428 G>A maps to NM_002662.3 T641T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:24838060 G>T maps to NM_001130726.2 Y244*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:25235820 C>A maps to NM_018323.3 S12S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr4:36152574 G>T maps to NM_015230.2 I948I. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-P4-A5EB-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr5:75888709 G>A maps to NM_006633.2 L289L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr5:178050362 C>A maps to NM_020666.2 G19*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:32016287 C>T maps to ENST00000375244 A3299A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:99823845 T>A maps to NM_017421.3 T233T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr6:149997826 C>G maps to NM_004690.2 G880G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:5781126 G>C maps to NM_207111.2 S174*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:83739848 G>A maps to NM_006080.2 Y130Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:99158260 C>T maps to NM_001083956.1 L27L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:107545819 T>C maps to NM_000108.3 N151N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr7:139258059 C>A maps to NM_022740.4 P1070P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr8:86057650 G>T maps to NM_033402.4 E1002*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr9:26925950 C>A maps to NM_001031689.2 V247V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chrX:76777833 C>A maps to NM_000489.3 G2294G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr12:111757855 C>T maps to NM_015267.3 N681N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr12:112096634 G>A maps to NM_006768.3 R376*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr12:116428912 C>T maps to NM_015335.4 G1282G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr15:65628244 A>G maps to NM_004884.3 G153G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr17:72340926 C>A maps to NM_153209.3 R204R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr19:1986957 G>A maps to NM_017797.3 S429S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr19:34710314 T>G maps to NM_001114093.1 A267A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr4:3494663 A>C maps to ENST00000389653 P317P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr4:85675020 T>C maps to NM_014991.4 Q1856Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr5:7878350 A>C maps to NM_024010.2 V259V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr5:122154606 T>G maps to NM_003100.2 L367L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr6:2955760 G>C maps to ENST00000316782 L136L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr9:14770685 G>T maps to ENST00000380880 S1662*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr9:32633309 G>A maps to NM_153809.2 G756G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chr9:37800964 G>T maps to NM_024345.3 P34P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-P4-A5ED-01A-11D-A28G-10 chrX:106034464 G>A did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:2238152 G>A maps to NM_003036.3 R712R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:35331686 C>T maps to NM_001080418.1 L979L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:226075305 G>T maps to ENST00000419724 G285G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr1:249106347 G>C maps to NM_030645.1 A311A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr10:121212788 G>A did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr11:18195096 C>T maps to NM_054032.3 L98L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr12:113610194 G>A maps to NM_001111322.1 S414S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr15:74281092 A>G maps to NM_004809.3 F147F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:13980320 A>G maps to NM_001303.3 Q149Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:60753773 C>A maps to NM_006039.3 I572I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:62855781 A>T maps to NM_199340.2 I1494I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr18:13826447 G>A maps to NM_005913.2 A228A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr19:8527466 T>G did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr19:17837416 G>A maps to NM_018174.4 T408T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr19:53384826 A>G maps to NM_207333.2 T184T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:69207169 A>G maps to NM_019617.3 T161T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:172333420 T>A maps to NM_025000.3 S381S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr2:201438488 T>G maps to NM_152524.5 S1140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr21:43241556 C>T maps to NM_022115.3 L1008L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr22:50716443 T>C did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr7:26894414 A>G maps to NM_003930.3 D54D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr7:149518181 C>T maps to NM_198455.2 C4179C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr9:139907276 C>G maps to ENST00000355090 V1686V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:36552573 C>T maps to NM_014466.2 N225N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:67519573 C>A maps to NM_015139.2 L41L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:78194349 T>C maps to NM_015017.3 E286E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:94546178 G>A maps to NM_000350.2 I318I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr1:234743059 G>A maps to NM_182972.2 F529F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr10:88703694 G>A maps to NM_024756.2 A282A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr10:134036391 C>T maps to NM_173575.2 K364K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr12:57894253 G>C maps to NM_004990.2 R414R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr15:40056079 C>T maps to NM_152597.4 E167E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr15:41689068 G>A maps to NM_016013.2 H63H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr17:39658843 T>C maps to NM_153490.2 K342K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr19:8038747 G>A maps to ENST00000351593 R124R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr19:15227274 G>T maps to NM_006844.3 A415A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr2:219536684 C>G maps to NM_022453.2 A3A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr22:36702091 G>T maps to NM_002473.4 G681G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr3:47164504 G>T maps to NM_014159.6 R541R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr3:53913971 T>C maps to NM_022899.4 G96G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr4:13545663 G>A maps to NM_001189.3 L125L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr4:48037861 T>C maps to NM_207330.1 N302N. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-PJ-A5Z9-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr5:56170959 G>T maps to NM_005921.1 L596L. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-PJ-A5Z9-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-PJ-A5Z9-01A-11D-A28G-10 chr9:138594139 C>G maps to ENST00000298480 G12G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr1:152777876 G>A maps to NM_178351.3 T26T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr1:152883268 A>G maps to NM_005547.2 Q332Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr1:204985553 G>T maps to ENST00000367172 E1311*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr11:57182148 G>A maps to ENST00000428603 P346P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:95867963 T>G maps to NM_006838.3 G3G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:110969391 A>G maps to NM_152442.3 K416K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:114385204 G>A maps to NM_016196.3 F447F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr12:125509639 C>A maps to NM_080626.5 S140S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr13:21306118 T>C maps to NM_174928.1 P123P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr13:99092298 T>A did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr14:77580237 C>T maps to NM_033426.2 F259F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr14:93408016 C>T maps to NM_014216.4 A378A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr15:52500780 G>T maps to NM_018728.3 L1452L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr15:75982865 G>C maps to NM_001897.4 L180L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr16:4557976 C>T maps to NM_001127205.1 R156R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr16:68267895 C>G did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:7287557 T>C maps to NM_003985.3 P284P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:39274237 A>G maps to NM_033059.3 C110C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:39324103 A>G maps to NM_033187.1 S107S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:40765684 C>T maps to NM_001070.4 A209A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr17:79860377 A>G maps to NM_148896.3 Q75Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:991961 C>T maps to NM_024100.3 V313V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:38056036 G>A maps to NM_016536.3 G431G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:39226802 G>A maps to NM_144691.3 G510G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr19:51831096 C>A maps to NM_001101372.1 A293A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr2:233671360 T>A maps to ENST00000373566 P622P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr2:237272539 C>T maps to ENST00000457693 L592L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr21:28338044 A>T maps to NM_007038.3 A222A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:113376121 C>T maps to NM_001009899.2 Q1469Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:113376127 C>T maps to NM_001009899.2 Q1467Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:135825107 T>C maps to NM_002718.4 A1091A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:150421589 T>C maps to NM_152394.3 E32E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:185960323 T>A maps to NM_001346.2 R599*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:195505793 T>G maps to NM_018406.5 T4219T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:195509339 G>A maps to NM_018406.5 H3037H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr3:195512486 G>A maps to NM_018406.5 T1988T. Only missense variants will be evaluated by CHASM.
Multiple mappings detected for codon TCGA-Q2-A5QZ-01A-11D-A28G-10. Mapping will be selected arbitrarily.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr4:88536435 C>T maps to NM_014208.3 S874S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr5:475167 G>A maps to NM_004174.2 P777P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr5:14601481 G>A maps to NM_019018.2 E93E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr5:170736389 G>A maps to NM_021025.2 A7A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:137113271 G>A maps to NM_005923.3 G8G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:142741041 C>T maps to NM_198569.2 F1040F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:161413040 G>A maps to NM_005922.2 P26P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr6:170893453 C>T maps to NM_002598.3 P72P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr7:49815180 C>T maps to NM_198570.3 H50H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr7:98990334 C>T maps to NM_005720.2 A275A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr7:128415146 C>T maps to NM_001708.2 K138K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr8:39550200 T>A did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr9:71628294 G>A maps to NM_002732.3 P238P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chrX:132092309 C>A maps to NM_001077188.1 L107L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chrX:152938522 C>A maps to NM_001039582.3 L86L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr1:19597049 C>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chrX:70523524 G>T maps to NM_012278.1 G173*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr16:1398015 C>G maps to NM_003933.4 Y1084*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr20:57611628 C>T did not map to a codon.
Sequencing variant TCGA-A4-8517-01A-11D-2396-08 chr17:4837203 C>T maps to NM_000173.5 T435T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8518-01A-11D-2396-08 chr1:205350720 T>G did not map to a codon.
Sequencing variant TCGA-A4-A4ZT-01A-11D-A26P-10 chr7:74298938 G>C did not map to a codon.
Sequencing variant TCGA-A4-A5Y0-01A-11D-A31X-10 chr1:220231486 T>C did not map to a codon.
Sequencing variant TCGA-A4-A5Y1-01A-11D-A28G-10 chr2:186671592 C>T maps to NM_173651.2 Q5943*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3466-01A-01D-1252-08 chr20:3641541 G>A maps to NM_145762.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr17:18446395 G>A did not map to a codon.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr9:89560845 C>G maps to NM_002048.2 P283P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-A47M-01A-11D-A25F-10 chr9:21481035 C>T did not map to a codon.
Sequencing variant TCGA-B1-A655-01A-11D-A31Z-10 chr1:220231329 T>C did not map to a codon.
Sequencing variant TCGA-B1-A656-01A-11D-A31X-10 chr7:107556127 A>T maps to NM_000108.3 K288*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr12:49426525 G>A maps to NM_003482.3 Q3988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr12:13529115 C>T did not map to a codon.
Sequencing variant TCGA-B9-A44B-01A-11D-A25F-10 chr7:74300941 C>T did not map to a codon.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr2:186671551 C>G maps to NM_173651.2 S5929*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr20:3641290 A>C maps to NM_145762.2 P203P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr20:3641541 G>A maps to NM_145762.2 L147L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr2:186671399 T>C maps to NM_173651.2 D5878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr2:211057526 C>G did not map to a codon.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:16889991 G>A did not map to a codon.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr1:227920038 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7046-01A-11D-1961-08 chr7:72420538 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr11:63283876 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr10:122610929 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr11:77781011 G>T did not map to a codon.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr15:55651609 C>A did not map to a codon.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr19:43013184 G>T did not map to a codon.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr20:30156072 C>A did not map to a codon.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr4:100140380 A>G did not map to a codon.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr7:72419165 G>A did not map to a codon.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr15:90293901 G>T maps to NM_018670.3 R187R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr22:42908104 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr5:131679547 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr1:100159630 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr2:74685002 C>A did not map to a codon.
Sequencing variant TCGA-DZ-6132-01A-11D-1961-08 chr6:132859937 G>T maps to NM_175057.3 T170T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr13:41384826 G>T did not map to a codon.
Sequencing variant TCGA-DZ-6133-01A-11D-1961-08 chr9:19093291 C>A maps to NM_017645.3 G105*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr17:4837737 A>G maps to NM_000173.5 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chr17:46675549 G>T did not map to a codon.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr11:67119434 G>C did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr5:92956597 A>G did not map to a codon.
Sequencing variant TCGA-G7-6789-01A-11D-1961-08 chr20:44004244 C>A did not map to a codon.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr17:46627633 C>A did not map to a codon.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr9:17010 T>C maps to NM_182905.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6793-01A-11D-1961-08 chr20:44517380 G>T did not map to a codon.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr11:66330356 C>A maps to NM_001104.1 R827R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr2:219128022 C>A maps to NM_170699.2 A192A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:186265990 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr1:10408754 G>T maps to ENST00000377086 E1305*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr11:63177376 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr12:54367012 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr15:37100692 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr17:6913790 A>G did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:74685021 C>A did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr2:186673772 C>A maps to NM_173651.2 S6669S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr22:50903273 C>A maps to ENST00000337034 E479*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:6588957 G>T did not map to a codon.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr6:10942739 C>A maps to NM_001040274.2 S621*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr7:66767733 C>A did not map to a codon.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr7:66774511 T>G did not map to a codon.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr1:23697670 C>A did not map to a codon.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr5:121799287 C>G did not map to a codon.
Sequencing variant TCGA-GL-A59R-01A-11D-A26P-10 chr1:220231329 T>C did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr19:14261618 C>A did not map to a codon.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr2:179368699 C>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr15:91510299 C>A did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr17:37224005 G>T did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr2:227919408 C>A maps to ENST00000396625 G921*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-A5NK-01A-11D-A26P-10 chr1:23696042 A>C maps to ENST00000507744 R85R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-A6M8-01A-11D-A31X-10 chr18:21214113 C>T did not map to a codon.
Sequencing variant TCGA-IZ-A6M9-01A-11D-A31X-10 chr1:220231329 T>C did not map to a codon.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr1:13497725 A>C maps to NM_001045480.1 G341G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-MH-A55W-01A-11D-A26P-10 chr1:220231274 T>C did not map to a codon.
Sequencing variant TCGA-MH-A561-01A-11D-A26P-10 chr6:91226400 C>T did not map to a codon.
Sequencing variant TCGA-P4-A5E8-01A-11D-A28G-10 chr2:39964199 C>G did not map to a codon.
Sequencing variant TCGA-P4-A5EB-01A-11D-A28G-10 chr9:21482027 G>A did not map to a codon.
Sequencing variant TCGA-PJ-A5Z8-01A-11D-A28G-10 chr17:18454788 T>A did not map to a codon.
Sequencing variant TCGA-Q2-A5QZ-01A-11D-A28G-10 chr22:19137289 G>A maps to NM_005315.1 F133F. Only missense variants will be evaluated by CHASM.
