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 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 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 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 chr2:139308571 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 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 chr15:25959388 C>G did not map to a codon.
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 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 chr4:78082687 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 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 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 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 chr20:49367022 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 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 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 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 chr2:24991158 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 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 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 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 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 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 chr4:3441323 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 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 chr3:38159472 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 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 chr8:110131437 G>A maps to NM_003301.4 P317P. 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 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 chr1:203832834 G>A maps to NM_003094.2 R42R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7287-01A-11D-2136-08 chr1:203832834 G>A maps to NM_003094.2 R42R. Only missense variants will be evaluated by CHASM.
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 chr1:100327976 C>G maps to ENST00000311030 S154*. 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 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 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 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 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 chr6:26104204 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 chr6:76660635 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 chr6:76660635 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 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 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 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 chr12:54764719 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 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 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 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 chr6:76660532 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 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 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 chr17:40717243 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 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 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:123197833 C>A maps to NM_001042750.1 S653*. 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 chr8:109462082 A>G maps to NM_014673.3 E24E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr8:109462082 A>G maps to NM_014673.3 E24E. 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 chr12:6649693 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 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 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 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 chr7:72416769 G>A maps to ENST00000434423 K1249K. 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 chr15:43299482 C>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 chr12:53685604 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 chr15:90634782 A>G 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 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 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 chr11:26725401 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 chr7:148702374 C>T maps to NM_004911.4 G460G. 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-A4-7288-01A-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 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 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 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 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 chr11:47605942 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 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 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 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 chr19:1468066 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 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 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 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 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 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 chr3:145803002 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 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 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 chr12:46285792 G>A did not map to a codon.
Sequencing variant TCGA-A4-7288-01A-11D-2136-08 chr12:46285792 G>A did not map to a codon.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:73471794 G>T maps to NM_006429.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:73471794 G>T maps to NM_006429.3 L190L. 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 chr5:67576766 T>G maps to ENST00000396611 T283T. 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 chr4:47538505 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 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 chr6:110746233 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 chr6:31922208 T>C maps to ENST00000375425 S258S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr6:31922208 T>C maps to ENST00000375425 S258S. 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 chr7:13971322 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 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 chr4:114434487 G>A maps to ENST00000515496 F314F. 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 chr21:37418116 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 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 chr7:92151472 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 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 chr12:112183961 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 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 chr11:118869165 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 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 chr1:86890014 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 chr14:23374813 C>G did not map to a codon.
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 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 chr2:203155145 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 chr2:73471795 C>T maps to NM_006429.3 Q191*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7583-01A-11D-2136-08 chr2:73471795 C>T maps to NM_006429.3 Q191*. 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 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 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 chr2:179411555 A>G maps to NM_133378.4 D28965D. 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 chr12:14772232 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 chr19:13996868 C>G did not map to a codon.
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 chr15:45456067 T>A maps to NM_175940.1 R1495R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr15:45456067 T>A maps to NM_175940.1 R1495R. 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 chr1:54870253 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 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 chr12:41316145 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 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 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 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 chr19:35828751 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 chr4:54266006 G>C did not map to a codon.
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 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 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 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 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 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 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 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 chr12:78604233 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 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 chr2:109109238 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 chr2:207040929 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 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 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 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 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 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 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 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 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 chr18:23670482 A>G maps to ENST00000415083 T20T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr18:23670482 A>G maps to ENST00000415083 T20T. 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 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 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 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 chr2:238722325 G>T did not map to a codon.
Sequencing variant TCGA-A4-7584-01A-11D-2136-08 chr2:238722325 G>T did not map to a codon.
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 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 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 chr1:32207415 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 chr1:26149566 T>A maps to ENST00000336146 P16P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr1:26149566 T>A maps to ENST00000336146 P16P. 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 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 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 chr1:150258999 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 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 chr15:65295423 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 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 chr7:36396612 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 chr1:198704381 G>A did not map to a codon.
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 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 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 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 chr1:162344113 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 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 chr2:149835495 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 chr2:99720472 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 chr2:99720472 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 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 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 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 chr5:7867620 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 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 chr1:190067268 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 chr9:137734001 G>C did not map to a codon.
Sequencing variant TCGA-A4-7585-01A-11D-2136-08 chr9:137734001 G>C did not map to a codon.
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 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 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 chr17:58740445 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 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 chr12:53097169 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 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 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 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 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 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 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 chr1:46086773 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 chr2:136736936 C>A did not map to a codon.
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 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 chr9:129595384 G>T maps to NM_014007.3 S199S. 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 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 chr8:144801160 A>T did not map to a codon.
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 chr11:118969111 C>T 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 chr15:65625619 C>T maps to NM_004884.3 T319T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr15:65625619 C>T maps to NM_004884.3 T319T. Only missense variants will be evaluated by CHASM.
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 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 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 chr1:94548961 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 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 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 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 chr1:114402064 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 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 chr7:103029856 G>A maps to ENST00000354356 A442A. Only missense variants will be evaluated by CHASM.
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-A4-7732-01A-11D-2136-08 chr9:32988091 T>A maps to NM_001195248.1 K71*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr3:125651508 A>G maps to NM_001195223.1 L68L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7732-01A-11D-2136-08 chr3:125651508 A>G maps to NM_001195223.1 L68L. 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 chr10:74095535 A>T did not map to a codon.
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 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 chr17:1370771 A>C did not map to a codon.
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 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 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 chr2:21251316 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 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 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 chr15:64454354 T>C did not map to a codon.
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 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 chr1:91406115 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 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 chr4:89410408 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 chr3:27297797 G>A maps to ENST00000396636 I693I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr3:27297797 G>A maps to ENST00000396636 I693I. 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 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 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 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 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 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 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 chr10:63852306 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 chr3:42727130 G>A maps to NM_152393.2 Q7Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-11D-2136-08 chr3:42727130 G>A maps to NM_152393.2 Q7Q. 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-A4-7734-01A-11D-2136-08 chr9:125582791 G>A maps to NM_005388.4 Q160*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7734-01A-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 chr17:79425868 G>T maps to ENST00000436173 E1827*. 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 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 chr5:52366068 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 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 chr17:48734447 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 chrX:152960546 C>T maps to NM_005629.3 Q596*. 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-A4-7828-01A-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 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 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 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 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 chr12:54857069 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 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 chr5:140307712 A>G maps to NM_018898.3 Q412Q. Only missense variants will be evaluated by CHASM.
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 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 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 chr1:6639490 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 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 chr19:4290584 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 chr11:92917686 C>A did not map to a codon.
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 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 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 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 chr7:33136130 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 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 chr11:66444484 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 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 chr10:89501011 C>T maps to NM_001015880.1 D369D. 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 chr7:103159948 T>C maps to ENST00000428762 L2561L. 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 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 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 chr11:61081865 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 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 chr1:55612676 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 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 chr6:51930864 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 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 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 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 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 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 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 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 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 chr11:65423174 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 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 chr8:53570006 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 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 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 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 chr2:162227814 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 chr12:47628908 G>T maps to NM_138371.1 L21L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr12:47628908 G>T maps to NM_138371.1 L21L. 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 chr19:7810713 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 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 chr2:102849532 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 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 chr1:152082278 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 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 chr9:2718278 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 chr6:32548010 T>G did not map to a codon.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr6:32548010 T>G did not map to a codon.
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 chr19:40419756 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 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 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 chr9:127572162 C>T maps to NM_182487.2 Y477Y. 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-A4-7996-01A-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 chr19:15350518 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 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 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 chr16:2905587 G>A maps to NM_022119.3 S182S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-7996-01A-11D-2201-08 chr16:2905587 G>A maps to NM_022119.3 S182S. 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 chr18:47800702 C>T maps to ENST00000424334 R384R. 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 chr11:108155201 T>C did not map to a codon.
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 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 chr9:16419220 A>G maps to NM_017637.5 S1022S. 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-A4-7997-01A-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 chr20:419912 G>T maps to ENST00000246077 V290V. 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 chr1:209974722 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 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 chr21:27348293 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 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 chr1:226127229 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 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 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 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 chr3:56787576 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 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 chr8:10470572 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 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 chr15:64021463 C>T maps to ENST00000261887 W1042*. Only missense variants will be evaluated by CHASM.
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 chr12:6138618 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 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 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 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 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 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 chr10:73055665 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 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 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 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 chr1:145761287 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 chr1:46290208 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 chr1:46290208 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 chr1:234744250 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 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 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 chr15:52446238 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 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 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 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 chr12:132405712 C>G maps to NM_003565.2 A1010A. 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 chr1:151109385 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 chr12:54856510 T>A did not map to a codon.
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 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 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 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 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 chr16:89169103 G>A maps to NM_174917.2 A253A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr16:89169103 G>A maps to NM_174917.2 A253A. 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 chr2:37365710 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 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 chr5:74026106 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 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 chr19:7615222 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 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 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 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 chr17:34077158 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 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 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 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 chr2:107032392 G>A maps to ENST00000304514 L1659L. 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 chr11:82877723 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 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 chr5:74981181 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 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 chr1:169806132 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 chr1:167096128 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 chr1:167096128 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 chr11:77580811 G>A maps to NM_024684.2 E59E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8098-01A-11D-2396-08 chr11:77580811 G>A maps to NM_024684.2 E59E. 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 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 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 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 chr14:24032847 C>T did not map to a codon.
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 chr16:56485679 T>C did not map to a codon.
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 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 chr2:98413328 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 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 chr17:45056016 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 chr17:65665780 T>C did not map to a codon.
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 chr5:140724209 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 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 chr16:31098020 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 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 chr9:136305498 G>T maps to NM_139025.3 G607G. 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 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 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 chr4:52765462 T>C maps to ENST00000451288 N222N. 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 chr17:40025022 T>C maps to ENST00000401700 E1094E. 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 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 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 chr15:59515312 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 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: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 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 chr8:17419588 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 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 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 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 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 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 chr17:8350136 T>C maps to ENST00000402554 S157S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr11:11373528 C>A did not map to a codon.
Sequencing variant TCGA-A4-8310-01A-11D-2396-08 chr11:11373528 C>A did not map to a codon.
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 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 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 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 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 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 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 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 chrX:70444363 C>T maps to NM_000166.5 T269T. 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-A4-8310-01A-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 chr8:132052525 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 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 chr9:86587098 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 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 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 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 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 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 chr16:14755822 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 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 chr2:220239738 G>A maps to NM_012100.2 L415L. 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 chr17:38926070 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 chr1:10678474 G>A did not map to a codon.
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 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 chr5:101834203 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 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 chr16:568987 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 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 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 chr11:65788965 C>T did not map to a codon.
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 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 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 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 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 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 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 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 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 chr19:48737763 A>G maps to NM_001184900.1 L82L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr19:48737763 A>G maps to NM_001184900.1 L82L. 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 chr11:63273899 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 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 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 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 chr4:983982 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 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 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 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 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 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 chr17:36099581 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 chrX:15682859 A>G maps to NM_020665.4 H13H. 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-A4-8311-01A-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 chr21:44589373 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 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 chr6:41129013 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 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 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 chr12:113534671 C>T maps to NM_004416.2 D597D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8311-01A-11D-2396-08 chr12:113534671 C>T maps to NM_004416.2 D597D. Only missense variants will be evaluated by CHASM.
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 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 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 chr17:80443513 C>T maps to ENST00000374611 V418V. 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.
Sequencing variant TCGA-A4-8312-01A-11D-2396-08 chr15:25972304 A>T did not map to a codon.
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 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 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 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 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 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 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 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 chr17:48600412 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 chr17:48600412 A>T maps to NM_032133.4 R500R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr13:31232331 T>C maps to NM_005800.4 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr13:31232331 T>C maps to NM_005800.4 L706L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr19:6926600 A>C maps to ENST00000381407 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr19:6926600 A>C maps to ENST00000381407 G739G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:100155331 T>C maps to NM_017890.3 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:100155331 T>C maps to NM_017890.3 I594I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr9:127990237 C>A maps to NM_005833.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr9:127990237 C>A maps to NM_005833.3 P192P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr20:2290998 C>A maps to NM_003245.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr20:2290998 C>A maps to NM_003245.3 S119S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:61769428 A>G maps to NM_017780.2 K2530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:61769428 A>G maps to NM_017780.2 K2530K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr9:109691964 T>A maps to NM_021224.4 R1924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr9:109691964 T>A maps to NM_021224.4 R1924R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr4:5827299 A>G maps to NM_001014809.1 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr4:5827299 A>G maps to NM_001014809.1 A630A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr11:58979711 G>T maps to NM_001039396.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr11:58979711 G>T maps to NM_001039396.1 V209V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:122626357 A>G maps to NM_005328.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:122626357 A>G maps to NM_005328.2 L550L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:94748605 A>G maps to NM_203390.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:94748605 A>G maps to NM_203390.2 P11P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:100147933 A>G maps to NM_017890.3 E512E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:100147933 A>G maps to NM_017890.3 E512E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr4:79832295 A>G maps to NM_198892.1 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr4:79832295 A>G maps to NM_198892.1 A865A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:28574532 G>A maps to NM_001440.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr8:28574532 G>A maps to NM_001440.2 L319L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr1:20141447 A>T maps to NM_019062.1 C49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr1:20141447 A>T maps to NM_019062.1 C49*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr1:24021147 A>T did not map to a codon.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr1:24021147 A>T did not map to a codon.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr2:225379450 G>T maps to NM_003590.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr2:225379450 G>T maps to NM_003590.3 V139V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr12:51856200 C>G maps to NM_001039960.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr12:51856200 C>G maps to NM_001039960.1 P403P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr17:48539813 T>C maps to ENST00000427954 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr17:48539813 T>C maps to ENST00000427954 D245D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr6:13595707 G>T did not map to a codon.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr6:13595707 G>T did not map to a codon.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr4:123814306 C>A maps to NM_007083.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr4:123814306 C>A maps to NM_007083.3 R209R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr3:170079129 A>T maps to NM_005414.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr3:170079129 A>T maps to NM_005414.3 G337G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr1:22165519 C>A maps to NM_005529.5 V3316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr1:22165519 C>A maps to NM_005529.5 V3316V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr17:56281675 T>C maps to NM_000502.4 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr17:56281675 T>C maps to NM_000502.4 G680G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr3:47461038 C>T maps to NM_012235.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr3:47461038 C>T maps to NM_012235.2 P573P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr18:77170517 G>T maps to NM_172387.1 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr18:77170517 G>T maps to NM_172387.1 P68P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr6:30668242 C>A maps to NM_014641.2 *2090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr6:30668242 C>A maps to NM_014641.2 *2090L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr5:122364998 C>G did not map to a codon.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr5:122364998 C>G did not map to a codon.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr14:64606709 T>C maps to NM_182914.2 H4965H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr14:64606709 T>C maps to NM_182914.2 H4965H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr3:74474020 G>A maps to NM_020872.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr3:74474020 G>A maps to NM_020872.1 L143L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr22:28315188 A>C did not map to a codon.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr22:28315188 A>C did not map to a codon.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr1:160385957 C>T maps to NM_020335.2 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr1:160385957 C>T maps to NM_020335.2 R60*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr6:157510845 A>C maps to ENST00000367148 P1247P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-A4-8516-01A-11D-2396-08 chr6:157510845 A>C maps to ENST00000367148 P1247P. 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 chr3:19389245 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 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 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 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 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 chr1:209878261 G>A did not map to a codon.
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 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 chr1:110774915 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 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 chr12:110813920 T>C maps to NM_016238.2 V520V. 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 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 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 chr1:33985174 T>A maps to ENST00000373381 T3573T. 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 chr12:51450185 G>A maps to ENST00000448283 L285L. 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 chr1:22310246 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 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 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 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 chr18:2718193 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 chr4:190874220 A>G did not map to a codon.
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 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 chr1:1480324 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 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 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 chr5:176471534 G>C did not map to a codon.
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 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 chr5:131953818 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 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 chr4:106967780 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 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 chr5:129241298 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 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 chr16:67236621 T>A maps to NM_024712.3 T550T. 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 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 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 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 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 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 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 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 chr12:9096394 A>G did not map to a codon.
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 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 chr10:1043229 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 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 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 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 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 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 chr6:27775402 C>T maps to NM_003519.3 E94E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr16:61891029 A>C maps to NM_001796.2 P220P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr16:61891029 A>C maps to NM_001796.2 P220P. 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-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-3467-01A-01D-1252-08 chr2:193056716 T>C did not map to a codon.
Sequencing variant TCGA-AL-3467-01A-01D-1252-08 chr2:193056716 T>C did not map to a codon.
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: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 chr16:88694028 G>C did not map to a codon.
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 chr2:138400115 C>T maps to ENST00000272643 C1289C. 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 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 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 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 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 chr12:9754097 T>C maps to NM_002258.2 S61S. 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 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 chr10:135440204 G>A maps to ENST00000443774 S14S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3468-01A-01D-1252-08 chr10:135440204 G>A maps to ENST00000443774 S14S. 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 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 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 chr19:50832051 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 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 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 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 chr10:91470808 A>G maps to ENST00000416354 K194K. 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 chr2:107049612 A>G maps to ENST00000304514 H778H. 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 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 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 chr20:3128939 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 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 chr3:52441416 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 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 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 chr7:100463707 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 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 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 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 chr22:21330825 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 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 chr2:46372318 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 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 chr7:74212377 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 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 chr19:54963392 T>G maps to ENST00000431846 A54A. 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 chr11:93090209 G>T did not map to a codon.
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 chr1:155408152 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 chr1:157557284 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 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 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 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 chr12:6494284 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 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 chr9:40774145 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 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 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 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 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 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 chr19:42872695 T>C maps to ENST00000251268 C2121C. 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 chr12:10978001 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 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 chr22:31837940 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 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 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 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 chr16:57494524 C>T maps to NM_020312.3 Q316*. 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 chr2:99689478 A>C did not map to a codon.
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 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 chr8:142480801 G>A maps to NM_207414.2 D689D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3472-01A-01D-1252-08 chr8:142480801 G>A maps to NM_207414.2 D689D. 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 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 chr17:17080726 G>A did not map to a codon.
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 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 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 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 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 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 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 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 chr5:139193772 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 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 chr17:10258305 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 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 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 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 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 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 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 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 chr20:44534918 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 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 chr9:130213581 G>A maps to NM_000976.2 F5F. 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 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 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 chr1:41503103 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 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 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 chr16:19073097 A>T did not map to a codon.
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 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 chr1:78959186 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 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 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 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 chr5:56542172 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 chr5:140188709 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 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 chr20:62598868 C>A maps to NM_020713.1 P43P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-3473-01A-01D-1252-08 chr20:62598868 C>A maps to NM_020713.1 P43P. 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 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 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 chr17:41365848 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 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 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 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 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 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 chr19:36362559 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 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 chr17:40726132 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 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 chr10:32560792 A>G maps to NM_025209.2 H709H. 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 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 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 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 chr1:8415615 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 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 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 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 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 chr6:57246848 G>T maps to NM_000947.2 L192L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr6:57246848 G>T maps to NM_000947.2 L192L. 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 chr12:111885275 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 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 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 chrX:73961091 C>T maps to NM_001008537.2 E1100E. 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-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 chr7:78131030 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 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 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 chr4:162697047 A>G maps to NM_020116.3 D196D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-AL-7173-01A-11D-2136-08 chr4:162697047 A>G maps to NM_020116.3 D196D. 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 chr14:24545746 G>A maps to NM_006032.2 P382P. 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 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 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 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 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 chr6:31778273 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 chr2:180311411 T>G maps to NM_152520.4 T252T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:180311411 T>G maps to NM_152520.4 T252T. 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 chr19:24309779 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 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 chr2:238234212 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 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 chr12:42858292 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 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 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 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 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 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 chrX:2826884 T>C did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chrX:2826884 T>C did not map to a codon.
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 chr5:140222315 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 chr5:31983431 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 chr5:31983431 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 chr17:45699223 C>T maps to NM_006310.3 R900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr17:45699223 C>T maps to NM_006310.3 R900*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr7:16837318 C>A did not map to a codon.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr7:16837318 C>A did not map to a codon.
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 chr12:62795033 T>A maps to ENST00000280377 T914T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr12:120653398 G>A maps to NM_001080855.1 G299G. 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.
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 chr2:166915108 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 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 chr14:75516129 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 chr7:20778603 A>G did not map to a codon.
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 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 chr2:70314949 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 chr14:102323021 G>A did not map to a codon.
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 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 chr2:182765432 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 chr2:227872133 C>T maps to ENST00000396625 Q1660Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr2:227872133 C>T maps to ENST00000396625 Q1660Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr10:62648932 T>A maps to NM_014836.4 R165*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B1-5398-01A-02D-1589-08 chr10:62648932 T>A maps to NM_014836.4 R165*. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-B1-5398-01A-02D-1589-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-B1-5398-01A-02D-1589-08. Mapping will be selected arbitrarily.
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 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 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 chr12:105433492 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 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 chr22:24226510 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 chr5:50683583 G>T did not map to a codon.
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 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 chr9:86485504 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 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 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 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 chr11:4904095 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 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 chr16:31090722 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 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 chr12:6707539 G>A maps to ENST00000309577 Q512*. 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 chr5:112458402 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 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 chr2:201478583 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 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 chr12:2909577 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 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 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 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 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 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 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 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 chr5:71739939 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 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 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 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 chr9:123591453 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 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 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 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 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 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 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 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 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 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 chr20:36989401 T>G maps to NM_004139.2 P211P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chr16:18844470 G>A maps to ENST00000389467 F2861F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr16:18844470 G>A maps to ENST00000389467 F2861F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 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-1252-08 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-1252-08 chr4:76532404 T>C maps to ENST00000307465 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr4:76532404 T>C maps to ENST00000307465 R168R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr22:39771986 A>C did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr22:39771986 A>C did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 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-1252-08 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-1252-08 chr8:42586818 C>T maps to NM_000749.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr8:42586818 C>T maps to NM_000749.3 G123G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 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-1252-08 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-1252-08 chr2:233681743 T>A did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr2:233681743 T>A did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chr11:7021929 C>T maps to NM_013249.2 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr11:7021929 C>T maps to NM_013249.2 E328E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr17:40725219 C>G did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr17:40725219 C>G did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chr15:72192124 T>G maps to ENST00000424560 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr15:72192124 T>G maps to ENST00000424560 R1125R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr4:146041305 G>A did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr4:146041305 G>A did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chrX:16685794 A>C maps to NM_001144002.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chrX:16685794 A>C maps to NM_001144002.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chr15:73590761 G>A maps to NM_002499.3 Q1325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 chr15:73590761 G>A maps to NM_002499.3 Q1325Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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 chr9:77598694 A>T maps to NM_152420.1 R406R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr9:77598694 A>T maps to NM_152420.1 R406R. 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 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 chr17:60766322 T>C did not map to a codon.
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 chr12:118599636 T>A maps to NM_016281.3 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr12:118599636 T>A maps to NM_016281.3 R699*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chr3:124515612 C>A maps to NM_002213.3 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1252-08 chr3:124515612 C>A maps to NM_002213.3 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chr2:131130763 C>T maps to NM_014369.3 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1252-08 chr2:131130763 C>T maps to NM_014369.3 P450P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chr17:2298596 T>G maps to NM_020310.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1252-08 chr17:2298596 T>G maps to NM_020310.2 A75A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1252-08 chr3:124515613 C>T maps to NM_002213.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1252-08 chr3:124515613 C>T maps to NM_002213.3 T438T. 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 chr14:52182104 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 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 chr9:14824064 T>G maps to ENST00000380880 V712V. 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chr12:49426525 G>A maps to NM_003482.3 Q3988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr12:49426525 G>A maps to NM_003482.3 Q3988*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr22:36013289 G>A maps to NM_203377.1 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr22:36013289 G>A maps to NM_203377.1 D5D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chr7:151879015 G>A maps to ENST00000355193 Q1977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr7:151879015 G>A maps to ENST00000355193 Q1977*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr15:51857283 C>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr15:51857283 C>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr5:251706 T>C did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr5:251706 T>C did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chr6:32947798 C>G maps to ENST00000395289 S714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr6:32947798 C>G maps to ENST00000395289 S714*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr15:95019964 C>A maps to NM_018349.3 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr15:95019964 C>A maps to NM_018349.3 S837S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chrX:123176468 C>T maps to NM_001042750.1 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chrX:123176468 C>T maps to NM_001042750.1 R146*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 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-1252-08 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-1252-08 chr1:1153924 G>A maps to NM_016176.3 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr1:1153924 G>A maps to NM_016176.3 D275D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 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-1252-08 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-1252-08 chr1:148025785 G>A maps to ENST00000310701 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr1:148025785 G>A maps to ENST00000310701 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr1:46494444 C>T maps to NM_015112.2 C686C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr1:46494444 C>T maps to NM_015112.2 C686C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 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-1252-08 chr3:9547648 G>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr3:9547648 G>A did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 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-1252-08 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-1252-08 chr6:32945958 C>G maps to ENST00000395289 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr6:32945958 C>G maps to ENST00000395289 P545P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 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-1252-08 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-1252-08 chr15:99670883 C>G maps to ENST00000336292 V772V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 chr15:99670883 C>G maps to ENST00000336292 V772V. 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 chr6:160157287 A>T did not map to a codon.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr10:122618294 C>A maps to NM_018117.11 A113A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1458-08 chr10:122618294 C>A maps to NM_018117.11 A113A. 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 chr22:19164389 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 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 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 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 chr3:58089734 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 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 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 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 chr3:51667681 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 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 chr11:55418711 C>T maps to NM_001004059.2 F111F. 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 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 chrX:53589173 C>T maps to ENST00000276009 E2412E. 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-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 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 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 chr17:60484527 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 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 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 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 chr15:30008819 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 chr17:73498793 A>G maps to NM_020753.3 T787T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr17:73498793 A>G maps to NM_020753.3 T787T. 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 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 chr2:32475306 C>T maps to NM_021209.4 E542E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-8121-01A-21D-2396-08 chr2:32475306 C>T maps to NM_021209.4 E542E. 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 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 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 chr3:149678839 C>T maps to NM_007282.4 V365V. 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 chr19:22817126 T>G did not map to a codon.
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 chr7:35912376 G>A did not map to a codon.
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 chr17:66270211 C>A did not map to a codon.
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 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 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 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 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 chr19:2216710 G>A maps to ENST00000221482 L785L. 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 chr1:207105905 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 chr7:102040094 G>A maps to NM_024653.3 K102K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr7:102040094 G>A maps to NM_024653.3 K102K. 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 chr19:15164632 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 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 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 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 chr12:41585334 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 chr21:47626683 T>G did not map to a codon.
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 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 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 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 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 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 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 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 chr1:22927185 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 chr1:11273602 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 chr1:11273602 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 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 chr2:27565919 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 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 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 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 chr15:43724400 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 chr7:149129442 C>T maps to ENST00000440594 E641E. Only missense variants will be evaluated by CHASM.
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-B9-4113-01A-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 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 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 chr4:115767017 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 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 chr5:150660716 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 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 chr15:41146020 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 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 chr4:89039326 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 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 chr2:42488419 T>C maps to NM_019063.3 A166A. 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 chr17:37876079 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 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 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 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 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 chr11:64889267 G>T maps to NM_001997.4 R6R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr11:64889267 G>T maps to NM_001997.4 R6R. 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 chr4:5721078 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 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 chr2:202262966 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 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 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 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 chr5:9119219 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 chr4:44449784 G>A maps to NM_198353.2 L252L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4114-01A-01D-1252-08 chr4:44449784 G>A maps to NM_198353.2 L252L. 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 chr8:99441266 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 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 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 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 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 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 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 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 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 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 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 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 chr11:1466622 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 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 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 chr9:133748370 C>T maps to NM_007313.2 A363A. 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-B9-4114-01A-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 chr1:94054730 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 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 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 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 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 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 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 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 chr5:34757667 C>T maps to NM_001145521.1 A44A. 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 chr5:134002686 G>A did not map to a codon.
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 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 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 chr4:84243393 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 chr4:3201561 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 chr4:3201561 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 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 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 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 chr20:19956189 C>T maps to ENST00000255006 F556F. 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 chr14:95556879 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 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 chr1:27428599 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 chr1:85491699 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 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 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 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 chr14:68282658 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 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 chr11:6486811 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 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 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 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 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 chr4:159092401 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 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 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 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 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 chr19:41223384 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 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 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 chr12:10233938 C>T maps to NM_016511.2 T96T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4115-01A-01D-1252-08 chr12:10233938 C>T maps to NM_016511.2 T96T. 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 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 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 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 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 chr1:27121058 C>T maps to NM_017837.2 F178F. 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 chr22:18028579 T>A maps to ENST00000400579 P1180P. 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 chr7:151262971 C>T 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 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 chr7:97933660 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 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 chr11:65305493 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 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 chr20:5903026 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 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 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 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 chr3:110830988 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 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 chr1:231502191 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 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 chr3:49946455 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 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 chr17:4800539 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 chr17:15964733 A>G maps to ENST00000395857 S1969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr17:15964733 A>G maps to ENST00000395857 S1969S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:47864025 G>A maps to NM_021035.2 H1845H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr20:47864025 G>A maps to NM_021035.2 H1845H. 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 chr3:69096706 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 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 chr16:56531662 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 chr7:2020095 G>A maps to NM_003550.2 D499D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4116-01A-01D-1252-08 chr7:2020095 G>A maps to NM_003550.2 D499D. 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 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 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 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 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 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 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 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 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 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 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 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 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 chr20:21376575 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 chr4:80992808 C>A did not map to a codon.
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 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 chr17:7324266 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 chr11:133805657 C>T did not map to a codon.
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 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 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 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 chr16:19884047 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 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 chr4:39325031 C>T maps to ENST00000381897 E216E. 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 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 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 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 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 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 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 chr17:40344971 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 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 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 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 chr19:53668283 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 chr19:40366037 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 chr19:40366037 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 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 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 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 chr19:39039029 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 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 chr6:17507927 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 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 chr19:5131902 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 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 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 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 chr2:105858581 C>G maps to NM_007227.3 P89P. 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 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 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 chr3:44776080 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 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 chr17:7230248 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 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 chr1:21585299 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 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 chr11:66411449 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 chr11:46897383 G>A maps to ENST00000256991 Q1269*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4617-01A-01D-1252-08 chr11:46897383 G>A maps to ENST00000256991 Q1269*. 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 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 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 chr1:27682528 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 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 chr12:124093347 A>T maps to NM_020936.1 R175*. 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 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 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 chr17:18220176 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 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 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 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 chr1:18023595 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 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 chr5:112200370 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 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 chr6:32147441 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 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 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 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 chr1:90179253 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 chr17:40714933 T>C maps to NM_001042532.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr17:40714933 T>C maps to NM_001042532.2 P127P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr6:170871039 A>G maps to NM_003194.4 Q72Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr6:170871039 A>G maps to NM_003194.4 Q72Q. 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 chr7:103002481 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 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 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 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 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 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 chr5:140563849 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 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 chr19:1220438 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 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 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 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 chr15:63548781 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 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 chr9:98229470 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 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 chr11:1017454 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 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 chr6:74119026 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 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 chr7:90042217 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 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 chr12:51138541 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 chr17:40475090 G>A maps to NM_139276.2 L607L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5155-01A-01D-1589-08 chr17:40475090 G>A maps to NM_139276.2 L607L. 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 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 chr17:79411727 C>T maps to ENST00000436173 P849P. 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 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 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 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 chr2:15735616 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 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 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 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 chr6:17292211 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 chr6:51923119 C>A did not map to a codon.
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 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 chr1:85656154 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 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 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 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 chr9:123742456 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 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 chr20:30064535 G>A maps to NM_014012.4 L96L. 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 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 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 chr3:97852335 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 chr17:77077140 C>G maps to NM_001042573.1 L286L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr17:77077140 C>G maps to NM_001042573.1 L286L. 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 chr19:3527658 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 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 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 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 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 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 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 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 chr2:58431303 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 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 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 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 chr16:1815159 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 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 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 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 chr5:114515695 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 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 chr2:145156026 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 chr1:36354061 G>A maps to NM_012199.2 V20V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr1:36354061 G>A maps to NM_012199.2 V20V. 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 chr1:19166251 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 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 chr10:17107615 C>T maps to NM_001081.3 P1010P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr10:17107615 C>T maps to NM_001081.3 P1010P. 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 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 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 chr5:31323225 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 chr7:148767679 G>A maps to NM_152411.3 P728P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr7:148767679 G>A maps to NM_152411.3 P728P. 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 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 chr6:42851202 A>G maps to NM_198486.2 K45K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr6:42851202 A>G maps to NM_198486.2 K45K. 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 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 chr8:94797544 T>C maps to NM_153704.5 Y409Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-5156-01A-01D-1589-08 chr8:94797544 T>C maps to NM_153704.5 Y409Y. 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 chr19:50063189 C>G did not map to a codon.
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 chr12:102125408 T>C maps to ENST00000449403 Q204Q. 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 chr19:11144468 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 chr18:14513779 C>A maps to ENST00000444806 E472*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr18:14513779 C>A maps to ENST00000444806 E472*. 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 chr17:14005507 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 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 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 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 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 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 chr4:169931207 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 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 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 chr5:73136426 T>C maps to NM_001080479.2 S423S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-7268-01A-11D-2136-08 chr5:73136426 T>C maps to NM_001080479.2 S423S. 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 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 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 chr1:40029529 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 chr1:151259372 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 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 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 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 chr1:152957849 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 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 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 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 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 chr2:218712983 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 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 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 chr8:8235102 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 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 chr12:85449851 G>T maps to NM_001079910.1 V427V. 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 chr17:47299546 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 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 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 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 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 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 chr17:74772620 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 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 chr8:28209092 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 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 chr1:65895650 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 chr14:73412734 G>A maps to NM_015604.3 K226K. 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.
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-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-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 chr11:840427 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 chr11:77934563 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 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 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 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 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 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 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 chr17:7250506 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 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 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 chr2:162711596 T>G maps to NM_001178015.1 T178T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5875-01A-11D-1589-08 chr2:162711596 T>G maps to NM_001178015.1 T178T. 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 chr7:40134551 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 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 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 chr7:114299728 G>A did not map to a codon.
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 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 chr19:17396341 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 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 chr12:48538848 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 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 chr2:47300863 C>T maps to ENST00000394850 G817G. 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 chr1:32203281 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 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 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 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 chr12:118462709 C>A maps to NM_007370.4 S159*. 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 chr1:185984289 G>A did not map to a codon.
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 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 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 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 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 chr2:100015353 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 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 chr22:16287579 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 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 chr5:89989973 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 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 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 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 chr11:65113197 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 chrX:70643917 T>C did not map to a codon.
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 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 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 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 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 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 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 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 chr1:100572513 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 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 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 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 chr1:12327037 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 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 chr2:136873380 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 chr2:55566740 T>G maps to ENST00000436346 S459S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5876-01A-11D-1589-08 chr2:55566740 T>G maps to ENST00000436346 S459S. Only missense variants will be evaluated by CHASM.
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 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 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 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 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 chr5:16764478 G>T maps to NM_012334.2 A402A. 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 chr16:2817458 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 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 chr3:20187857 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 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 chr17:10366487 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 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 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 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 chr15:45445602 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 chr10:55626410 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 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 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 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 chr19:1986876 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 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 chr5:172410943 C>T maps to NM_003945.3 F27F. 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 chr3:41274904 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 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 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 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 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 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 chr2:20871055 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 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 chr10:75457453 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 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 chr14:23467860 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 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 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 chr5:446364 G>A maps to ENST00000315013 R25R. 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 chr10:44112495 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 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 chr16:48385616 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 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 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 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 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 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 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 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 chr5:137715372 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 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 chr1:6204187 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 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 chr5:136328173 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 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 chr6:34210571 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 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 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 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 chr6:148808751 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 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 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 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 chr12:10766046 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 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 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 chr15:87217501 A>G did not map to a codon.
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 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 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 chr10:23003186 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 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 chr2:179452052 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 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 chr11:5068081 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 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 chr6:112457350 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 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 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 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 chr3:51697405 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 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 chr2:207833967 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 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 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 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 chr10:55583105 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 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 chr11:1466526 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 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 chr3:33135654 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 chr7:97823559 C>T maps to NM_014916.3 I1261I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5878-01A-11D-1589-08 chr7:97823559 C>T maps to NM_014916.3 I1261I. 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-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 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 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 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 chr1:156105084 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 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 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 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 chr20:2998528 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 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 chr17:10554907 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 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 chr21:41143023 G>A maps to NM_001080444.1 V200V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5879-01A-11D-1589-08 chr21:41143023 G>A maps to NM_001080444.1 V200V. 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 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 chrX:132160220 A>C maps to NM_031907.1 P676P. 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 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 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 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 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 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 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 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 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 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 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 chr7:21468914 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 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 chr4:3124640 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 chrX:43702914 C>G did not map to a codon.
Sequencing variant TCGA-BQ-5880-01A-11D-1589-08 chrX:43702914 C>G did not map to a codon.
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 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 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 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 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 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 chr1:41976754 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 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 chr18:74622685 C>T maps to NM_007345.3 S906S. 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 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 chr7:102769232 T>C maps to ENST00000455523 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr7:102769232 T>C maps to ENST00000455523 S70S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5881-01A-11D-1589-08 chr6:170871042 G>A maps to NM_003194.4 Q73Q. Only missense variants will be evaluated by CHASM.
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 chr1:6399499 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 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 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 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 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 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 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 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 chr17:3977516 C>T maps to NM_015113.3 L1204L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr5:140683315 C>T maps to NM_031947.2 T39T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr5:140683315 C>T maps to NM_031947.2 T39T. 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 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 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 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 chr5:132084159 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 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 chr17:37579983 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 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 chr2:153471510 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 chr8:109489021 C>T maps to NM_014673.3 T201T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5882-01A-11D-1589-08 chr8:109489021 C>T maps to NM_014673.3 T201T. Only missense variants will be evaluated by CHASM.
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 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 chr17:74288034 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 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 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 chr1:168168188 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 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 chr16:31089678 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 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 chr7:36445952 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 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 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 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 chr16:23540827 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 chr8:130883631 C>A maps to NM_016623.3 E62*. 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-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 chr2:128918713 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 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 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 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 chr2:157367410 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 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 chr7:100681164 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 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 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 chr1:45120713 G>T maps to NM_024587.2 V117V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr1:19545820 C>T maps to NM_015047.1 K986K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr1:19545820 C>T maps to NM_015047.1 K986K. 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-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-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 chr11:984671 C>T maps to ENST00000332231 Q245*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5883-01A-11D-1589-08 chr11:126201298 G>T did not map to a codon.
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 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 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 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 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 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 chr3:40465426 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 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 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 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 chr3:46492032 A>G maps to NM_002343.3 S278S. 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 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 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 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 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 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 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 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 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 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 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 chr1:32100868 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 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 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 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 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 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 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 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 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 chr16:2122848 G>A 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 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 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 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 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 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 chr8:87226721 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 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 chr2:39285903 C>T maps to NM_005633.3 W85*. Only missense variants will be evaluated by CHASM.
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 chr8:25715867 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 chr20:57613689 C>T did not map to a codon.
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 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 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 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 chr3:10387741 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 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 chr4:125592786 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 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 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 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 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 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 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 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 chr22:39482534 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 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 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 chr13:29001982 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 chr8:71126195 A>C maps to NM_006540.2 P67P. 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-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 chr17:39658759 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 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 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 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 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 chr2:101670696 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 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 chr7:27856086 T>C maps to ENST00000409980 N652N. 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 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 chr2:73680676 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 chr2:73680676 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 chr7:92119226 T>C did not map to a codon.
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 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 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 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 chr7:91631867 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 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 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 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 chr11:75509460 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 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 chr1:46751889 T>G maps to ENST00000254454 S191S. 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 chr8:48826504 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 chr8:17401958 G>T did not map to a codon.
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 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 chr2:27440796 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 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 chr4:76877178 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 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 chr11:66260241 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 chr4:4199006 C>T maps to NM_177998.1 E518E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5885-01A-11D-1589-08 chr4:4199006 C>T maps to NM_177998.1 E518E. Only missense variants will be evaluated by CHASM.
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 chr1:36915922 C>T maps to ENST00000356637 E16E. 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 chr22:29627007 G>T did not map to a codon.
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 chr6:43226955 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 chr19:40395905 C>T maps to NM_003890.2 E2497E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr19:40395905 C>T maps to NM_003890.2 E2497E. 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 chr1:26671978 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 chr7:100681140 T>A maps to NM_001040105.1 G2148G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr7:100681140 T>A maps to NM_001040105.1 G2148G. 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 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 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 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 chr4:100787279 T>G did not map to a codon.
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 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 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 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 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 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 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 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 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 chr17:26948414 A>G did not map to a codon.
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 chr19:36831479 G>A maps to NM_020917.2 S416S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5886-01A-11D-1589-08 chr19:36831479 G>A maps to NM_020917.2 S416S. 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: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 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 chr12:49431829 A>T maps to NM_003482.3 A3103A. Only missense variants will be evaluated by CHASM.
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 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 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 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 chr7:7412962 C>T maps to NM_001037763.2 K858K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5887-01A-11D-1961-08 chr7:7412962 C>T maps to NM_001037763.2 K858K. 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-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-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 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 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 chr19:13988493 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 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 chr17:18149934 G>A maps to NM_002018.2 F1008F. Only missense variants will be evaluated by CHASM.
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 chr19:49703679 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 chr12:113704161 G>T did not map to a codon.
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 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 chr17:33679779 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 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 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 chrX:107978242 C>T maps to NM_003604.2 R444R. 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-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 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 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 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 chr19:841047 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 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 chr7:121681009 G>A maps to NM_002851.2 V1926V. 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 chr1:158912062 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 chr11:65480306 T>A did not map to a codon.
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 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 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 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 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 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 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 chr2:99978206 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 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: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-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-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 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 chr15:24923230 T>A maps to NM_018958.2 T739T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5889-01A-11D-1589-08 chr15:24923230 T>A maps to NM_018958.2 T739T. 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 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 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 chr12:75436983 G>T maps to NM_139137.2 G606G. 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 chr17:7755371 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 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 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 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 chr1:2540841 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 chr3:47143046 T>C did not map to a codon.
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 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 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 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 chr5:72743506 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 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 chr3:47032942 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 chr3:12192766 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 chr3:12192766 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 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 chr16:23083423 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 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 chr10:63699985 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 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 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 chr9:113013694 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 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 chr7:102110042 C>A maps to NM_152892.1 I417I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr7:102110042 C>A maps to NM_152892.1 I417I. 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 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 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 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 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 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 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 chr16:56792501 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 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 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 chr4:186545112 G>A maps to ENST00000355634 H586H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5890-01A-11D-1589-08 chr4:186545112 G>A maps to ENST00000355634 H586H. 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 chr6:35213119 G>A maps to ENST00000394681 K855K. 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 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 chrX:123200036 T>C maps to NM_001042750.1 L703L. 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-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 chr20:62642771 G>C maps to NM_012469.3 T480T. 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 chr5:136963989 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 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 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 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 chr6:42657390 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 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 chr20:23967128 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 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 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 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 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 chr22:19870862 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 chr19:22605146 A>C did not map to a codon.
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 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 chr5:140711927 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 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 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 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 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 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 chr22:21989094 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 chr21:45732007 C>T maps to NM_002626.4 S86S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-5891-01A-11D-1589-08 chr21:45732007 C>T maps to NM_002626.4 S86S. 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 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 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 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 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 chr13:22088515 C>T maps to NM_152726.2 V213V. 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 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 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 chr17:1673259 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 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 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 chr17:6597516 C>G did not map to a codon.
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 chr17:73237523 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 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 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 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 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 chr1:43317093 C>A maps to ENST00000442768 L186L. 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-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-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 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 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 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 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 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 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 chr5:63257392 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 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 chr17:9846495 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 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 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 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 chr5:70800507 C>T maps to NM_018429.2 Q768*. 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 chr15:65983019 C>T maps to ENST00000443035 V1304V. 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 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 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 chr8:113249530 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 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 chr19:34832920 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 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 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 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 chr8:59059733 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 chrX:101908966 C>A maps to NM_001184727.1 T42T. 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-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 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 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 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: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 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 chr11:113679908 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 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 chr8:142186772 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 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 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 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 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 chr9:2110311 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 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 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 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 chr8:67477039 T>A maps to NM_001080416.2 T717T. 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 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 chr8:144940740 C>T maps to NM_031308.1 A2227A. 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-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 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 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 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 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 chr17:72428209 C>G maps to NM_022036.2 P11P. 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 chr17:79870324 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 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 chr13:41766947 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 chr17:11593356 G>A maps to NM_001372.3 A1406A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr17:11593356 G>A maps to NM_001372.3 A1406A. 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 chr15:64966234 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 chr13:99540612 C>T did not map to a codon.
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 chr15:28090199 T>A did not map to a codon.
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 chr15:100871169 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 chr15:100871169 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 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 chr3:130673863 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 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 chr7:73752799 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 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 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 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 chr8:20107304 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 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 chr17:78293015 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 chr14:101201160 C>T maps to NM_003836.5 A360A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7044-01A-11D-1961-08 chr14:101201160 C>T maps to NM_003836.5 A360A. 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 chr5:32108144 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 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 chr19:55385757 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 chr1:150689612 C>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 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 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 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 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 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 chr19:18557589 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 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 chr16:55360381 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 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 chr19:16551693 A>G maps to ENST00000455140 G64G. 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 chr1:78444625 G>A maps to ENST00000436586 G21G. 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 chr8:110451258 G>A maps to ENST00000426474 K1298K. 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 chr7:82532015 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 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 chr6:2623683 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 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 chr1:70895505 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 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 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 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 chr17:42089523 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 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 chr1:94528185 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 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 chr9:131028576 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 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 chr18:31263417 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 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 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 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 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 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 chr9:119202961 G>T maps to ENST00000313400 V1236V. 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 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 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 chr14:20345256 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 chr5:147010973 A>G did not map to a codon.
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 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 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 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 chr16:2052643 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 chr16:3554720 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 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 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 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 chr18:9257290 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 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 chr9:138839742 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 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 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 chr3:46939562 G>T did not map to a codon.
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 chr4:38990525 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 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 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 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 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 chr10:134896355 C>T maps to ENST00000368577 P277P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7045-01A-31D-1961-08 chr10:134896355 C>T maps to ENST00000368577 P277P. 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 chr17:4451583 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 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 chr7:21737743 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 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 chr12:120150414 G>C maps to ENST00000392521 L1555L. 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 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 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 chr1:5935028 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 chr1:151509761 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 chr1:151509761 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 chr1:1638913 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 chr1:1638913 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 chr1:201034980 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 chr1:201034980 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 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 chr19:3525915 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 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 chr17:72436052 T>A maps to NM_022036.2 S91S. Only missense variants will be evaluated by CHASM.
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 chr12:48888592 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 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 chr3:171394618 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 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 chr22:17280835 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 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 chr11:12316189 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 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 chr17:74158076 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 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 chr6:43541218 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 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 chr1:169824949 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 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 chr10:81702147 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 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 chr6:152201892 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 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 chr2:178977554 C>T maps to ENST00000456670 N94N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7048-01A-11D-1961-08 chr2:128526505 C>A did not map to a codon.
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 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 chr1:117633171 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 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 chr6:150005369 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 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 chr14:35872503 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 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 chr17:56565508 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 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 chr12:12302075 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 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 chr21:32638550 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 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 chr6:44390389 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 chr6:154521108 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 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 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 chr17:72368138 C>A maps to ENST00000440684 P1226P. 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 chr1:186324771 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 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 chr11:119210070 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 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 chr12:70704757 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 chr10:111878342 A>G did not map to a codon.
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 chr4:185724471 A>T did not map to a codon.
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 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 chr21:31709824 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 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 chr15:81282036 G>A maps to NM_015154.1 C32C. 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: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 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 chr8:72129011 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 chr2:203395529 T>C maps to NM_001204.6 P327P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7049-01A-11D-1961-08 chr2:203395529 T>C maps to NM_001204.6 P327P. 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 chr20:30723908 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 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 chr17:38324636 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 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 chr8:42037494 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 chr11:119051967 T>A did not map to a codon.
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 chr11:82882882 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 chr11:82882882 A>G maps to NM_015885.3 P1228P. 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 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 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 chr15:39882094 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 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 chr7:116166676 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 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 chr12:56720459 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 chr12:72017887 A>T maps to NM_144982.4 L1501*. 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 chr14:20845480 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 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: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 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 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 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 chr11:119988940 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 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 chr2:154334998 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 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 chr3:52282682 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 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 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 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 chr17:56164456 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 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 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 chr15:90138744 T>C maps to NM_152259.3 D601D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr15:90138744 T>C maps to NM_152259.3 D601D. 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 chr6:41303623 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 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 chr5:139864823 T>C maps to ENST00000253810 H663H. 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 chr15:75664532 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 chr5:76028541 C>A maps to NM_001992.3 S164S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7051-01A-12D-1961-08 chr5:76028541 C>A maps to NM_001992.3 S164S. 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 chr19:14991894 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 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 chr8:99152323 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 chr8:55534828 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 chr8:55534828 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 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 chr7:21678589 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 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 chr4:57891053 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 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 chr10:51586275 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 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 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 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 chr12:7867785 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 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 chr22:43213793 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 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 chr5:54591350 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 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 chr11:118250227 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 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 chr1:214556992 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 chr1:42048584 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 chr1:42048584 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 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: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 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 chr1:52902540 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 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 chr12:2909051 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 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 chr6:31627424 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 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 chr5:140021511 G>A maps to ENST00000252100 L124L. 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 chr12:67699343 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 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 chr14:68118140 C>T maps to NM_006370.2 L220L. 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 chr4:6303093 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 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 chr3:23942483 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 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 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 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 chr15:35083347 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 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 chr11:66636375 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 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:101096013 T>A maps to ENST00000263032 K152*. 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 chr8:109215295 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 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 chr2:96781258 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 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 chr1:16258647 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 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 chr9:39140599 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 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 chr19:7976337 A>G maps to ENST00000425613 G360G. 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 chr10:73406334 C>T maps to ENST00000398860 Y475Y. 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 chr3:185146746 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 chr3:51457621 C>G maps to ENST00000273612 R934R. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7053-01A-11D-1961-08 chr3:51457621 C>G maps to ENST00000273612 R934R. 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 chr1:59125679 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 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 chr17:73746315 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 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 chr5:82406898 G>T maps to NM_022406.2 G64G. Only missense variants will be evaluated by CHASM.
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-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-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 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 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 chr11:64522810 G>A maps to NM_005609.2 Y263Y. Only missense variants will be evaluated by CHASM.
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 chr3:48602252 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 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 chr11:77412530 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 chr12:12311913 G>A maps to NM_002336.2 L880L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7056-01A-11D-1961-08 chr12:12311913 G>A maps to NM_002336.2 L880L. 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 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 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 chr1:53287195 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 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 chr12:12483323 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 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 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 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 chr17:11520830 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 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 chr7:75401235 G>C maps to NM_006072.4 T53T. 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 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 chr6:7889003 A>C maps to NM_030810.3 T299T. 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.
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 chr2:109379712 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 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 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 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 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 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 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 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 chr17:62500169 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 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 chr2:37280724 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 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 chr1:236195869 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 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 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 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 chr1:147086308 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 chr1:67423740 G>C did not map to a codon.
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 chr8:35541183 C>T maps to ENST00000416672 T230T. Only missense variants will be evaluated by CHASM.
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-7058-01A-11D-1961-08 chrX:63412032 A>G maps to NM_152424.3 D378D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7058-01A-11D-1961-08 chrX:63412032 A>G maps to NM_152424.3 D378D. 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 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 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 chr17:26490599 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 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 chr5:916036 C>T maps to NM_004237.3 S384S. 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 chr1:223984098 A>G maps to NM_001031685.2 N714N. 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.
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 chr1:184476744 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 chr1:184476744 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 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 chr12:2716230 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 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 chr17:6012934 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 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 chr3:87017992 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 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 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 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: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 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 chr1:16378295 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 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 chr19:51273913 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 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 chr6:25967010 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 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 chr14:81744520 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 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 chr1:15793928 C>T maps to ENST00000375924 Q267*. 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 chr2:55844409 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 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 chr11:120745882 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 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 chr15:77087750 A>T maps to ENST00000324767 R214R. 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 chr20:47691343 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 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 chr8:39044453 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 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 chr3:122414351 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 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 chr17:33289280 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 chr2:85549812 A>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 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 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 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 chr5:131976366 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 chr5:128983498 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 chr5:128983498 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 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 chr16:67233264 C>A maps to NM_024712.3 I65I. 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 chr16:67168084 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 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 chr7:48081006 C>A maps to ENST00000430738 L89L. 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 chr6:45390465 A>G maps to ENST00000359524 Q133Q. 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 chr3:52029444 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 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 chr16:31383748 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 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: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 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 chr3:160249254 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 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 chr17:10267724 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 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 chr1:22903098 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 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:44733230 A>T maps to NM_021140.2 K75*. 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 chr12:57389325 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 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 chr15:79264260 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 chr19:35757259 A>G did not map to a codon.
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 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 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 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 chr12:107154994 T>A maps to ENST00000357881 T661T. 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 chr3:52023048 G>C maps to ENST00000463937 L496L. 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:69637855 T>C did not map to a codon.
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 chr17:6375989 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 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 chr7:43581575 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 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 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 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 chr15:59501014 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 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 chr7:79842141 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 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 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 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 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 chr19:36253152 G>A did not map to a codon.
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 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: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 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 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 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 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 chrX:51486958 G>T maps to NM_018094.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chrX:51486958 G>T maps to NM_018094.4 P79P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr8:77617294 G>T maps to NM_024721.4 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr8:77617294 G>T maps to NM_024721.4 G324G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chrX:144904633 C>T maps to NM_001144010.2 L231L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chrX:144904633 C>T maps to NM_001144010.2 L231L. 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 chr3:52651554 C>T did not map to a codon.
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 chr6:35392131 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 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 chr15:79748656 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 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 chr12:7046364 C>G maps to NM_001940.3 S645S. 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 chr16:20787238 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 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 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 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 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 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 chr16:4029167 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 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 chr3:48459372 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 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 chr11:62489599 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 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 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 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 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 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 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 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 chr3:52432934 A>G maps to ENST00000273600 V4117V. 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 chr2:152512858 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 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 chr16:71789971 C>T maps to ENST00000423132 E416E. 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 chr17:34340314 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 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 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 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 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 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 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 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 chr1:110604110 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 chr1:100214267 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 chr1:100214267 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 chr1:10177625 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 chr1:10177625 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 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 chr5:176831340 G>A maps to NM_000505.3 L292L. 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-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-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 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 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 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 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 chr9:22006243 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 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 chr1:11346094 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 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 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 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 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 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 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 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 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 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 chr2:24930396 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 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 chr1:17609567 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 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 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 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 chr2:220338576 C>A maps to NM_005876.4 R1467R. 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 chr17:44845985 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 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 chr19:40478460 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 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 chr21:16337669 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 chr1:32100954 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 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 chr20:56227615 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 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 chr8:10390472 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 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 chr22:18021910 C>T maps to ENST00000400579 C672C. 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 chr17:18212207 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 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 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 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 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 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 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 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 chr18:65181491 A>G maps to NM_032160.2 N128N. 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 chr7:138145433 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 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 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 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 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 chr2:233244239 A>G maps to NM_001632.3 K109K. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7837-01A-11D-2136-08 chr2:233244239 A>G maps to NM_001632.3 K109K. 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 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 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 chr5:56177036 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 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 chr20:62078165 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 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 chr11:73066675 C>G maps to NM_014786.3 A1184A. 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 chr7:39446254 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 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 chr2:132236968 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 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 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 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 chr18:10471913 G>A maps to ENST00000423585 Q261Q. Only missense variants will be evaluated by CHASM.
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 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 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 chr17:3919675 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 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 chr2:74761482 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 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 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 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 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 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 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 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 chr18:21451429 G>T maps to ENST00000416669 V1603V. 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 chr7:44805817 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 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 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 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 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 chr3:47456624 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 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 chr18:14105674 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 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 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 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 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 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 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 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 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 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 chr7:129962494 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 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 chr16:51172850 A>G maps to ENST00000251020 H1094H. 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 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 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 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 chr10:127782636 C>G maps to NM_003474.4 G357G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7838-01A-11D-2136-08 chr10:127782636 C>G maps to NM_003474.4 G357G. 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 chr14:64633997 G>A maps to NM_182914.2 L5551L. 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 chr11:723295 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 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 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 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 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 chr17:37880218 T>C maps to NM_004448.2 L755L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7839-01A-11D-2136-08 chr17:37880218 T>C maps to NM_004448.2 L755L. 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 chr12:27787952 T>C maps to NM_003622.3 L59L. 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 chr5:140605206 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 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 chr10:24835171 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 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 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 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 chr2:61493233 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 chr17:7470322 G>A did not map to a codon.
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 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: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 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 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 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 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 chr1:114964231 G>C maps to NM_015906.3 P629P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7840-01A-11D-2136-08 chr1:114964231 G>C maps to NM_015906.3 P629P. 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 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 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 chr10:28270469 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 chr15:65223119 T>G did not map to a codon.
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 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: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 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 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 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 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 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 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 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 chr11:43905564 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 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 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 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 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 chr2:218713667 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 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 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 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 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 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 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 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 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 chr1:210267874 T>C maps to NM_001146261.1 S262S. 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 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 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 chr5:140753887 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 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 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 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 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 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 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 chr2:24107698 T>G maps to NM_017552.1 S240S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr2:24107698 T>G maps to NM_017552.1 S240S. 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 chr17:4575081 C>T maps to ENST00000301396 E1212E. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr17:79632530 C>T maps to NM_001039842.1 A48A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DW-7841-01A-11D-2136-08 chr17:79632530 C>T maps to NM_001039842.1 A48A. 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 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 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 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 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 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 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 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 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 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 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 chr5:80600584 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 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 chr17:27052950 G>T maps to NM_138463.3 S55S. Only missense variants will be evaluated by CHASM.
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 chr1:160181402 C>A maps to ENST00000368075 L44L. Only missense variants will be evaluated by CHASM.
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 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 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 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 chr11:76890089 G>T 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 chr9:114429093 G>A did not map to a codon.
Sequencing variant TCGA-DW-7842-01A-11D-2136-08 chr9:114429093 G>A did not map to a codon.
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 chr2:234173558 T>C maps to ENST00000392018 T137T. 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 chr12:9000290 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 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 chr16:66612902 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 chr6:152546983 C>A maps to NM_182961.2 E7075*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr6:152546983 C>A maps to NM_182961.2 E7075*. 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 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 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 chr4:87691258 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 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 chr8:30694448 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 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 chr2:55473594 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 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 chr11:1099776 T>C maps to ENST00000441003 P2458P. 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 chr12:64174891 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 chr7:87910313 C>A maps to NM_024636.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr7:87910313 C>A maps to NM_024636.2 G355G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr21:43413769 T>C maps to NM_020727.4 Q145Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6131-01A-11D-1961-08 chr21:43413769 T>C maps to NM_020727.4 Q145Q. 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 chr2:207171573 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 chr4:174225145 G>A did not map to a codon.
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 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 chr5:159781880 G>A maps to NM_031908.4 G91G. 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 chr17:76133811 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 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 chr2:112608403 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 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 chr1:53262038 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 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 chr13:38237840 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 chr19:54937847 A>G did not map to a codon.
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 chr19:42907052 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 chr19:42907052 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 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 chr4:88584222 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 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 chr12:96273431 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 chr7:2691877 T>C did not map to a codon.
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 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 chr1:39888511 C>T maps to ENST00000361689 A3301A. 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 chr11:9519249 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 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 chr17:46152377 G>A maps to ENST00000442683 L139L. 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 chr20:47741018 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 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 chr14:56079009 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 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 chr1:27739178 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 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 chr4:83557888 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 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 chr12:95603625 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 chr4:159756555 G>A did not map to a codon.
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 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 chr7:99690936 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 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 chr2:218678432 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 chr13:95271584 G>A did not map to a codon.
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 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 chr19:49950352 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 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 chr8:121170483 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 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 chr19:44570871 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 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 chr8:6302562 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 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 chr1:94522329 A>G maps to NM_000350.2 L737L. 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 chr1:156823724 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 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 chr12:124848290 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 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 chr2:231077476 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 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 chr12:30790087 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 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 chr4:4322598 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 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 chr19:46317978 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 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 chr6:30877828 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 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 chr2:217364691 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 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 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 chr3:133692537 G>C maps to NM_005630.2 S122S. 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.
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 chr17:38319004 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 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 chr16:20851090 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 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 chr6:157527599 G>A maps to ENST00000367148 K1815K. 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 chr9:35061056 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 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 chr2:102493543 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 chr2:158971731 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 chr2:158971731 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 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 chr1:44467232 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 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 chr6:32714065 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 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 chr1:217975147 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 chr6:30883014 G>A did not map to a codon.
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 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 chr1:151372077 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 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 chr3:66460689 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 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 chr4:79516548 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 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 chr1:1269264 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 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 chr3:49463423 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 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 chr17:16089948 G>C maps to ENST00000395857 S54*. 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 chr11:46637367 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 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 chr7:75617586 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 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 chr8:22488016 G>A maps to NM_018688.4 L79L. 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 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 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 chr6:34059741 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 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 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 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 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 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 chr7:63720696 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 chr7:100780345 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 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 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 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 chr14:55310764 C>T maps to NM_001024024.1 R241R. 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.
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 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 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 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 chr17:10426830 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 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 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 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 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 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 chr9:116151741 G>A maps to ENST00000277315 D268D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chrX:132458559 G>A maps to NM_001448.2 F108F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-DZ-6135-01A-11D-1961-08 chrX:132458559 G>A maps to NM_001448.2 F108F. 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 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 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 chr1:85491893 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 chr1:152552160 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 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 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 chr2:74128512 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 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 chr5:176522538 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 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 chr13:28143268 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 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 chr17:30815100 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 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 chr19:50393784 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 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 chr16:12618620 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 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 chr5:140049031 T>C maps to NM_017706.4 H315H. 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 chr16:30676957 G>C 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 chr5:1488542 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 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 chr2:64199371 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 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 chr16:354432 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 chr9:139908395 G>C maps to ENST00000355090 V1475V. 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-5901-01A-11D-1589-08 chr5:131729503 G>A did not map to a codon.
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 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 chr17:39742795 A>C maps to NM_000526.4 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr17:39742795 A>C maps to NM_000526.4 G97G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr1:44442959 G>A did not map to a codon.
Sequencing variant TCGA-EV-5901-01A-11D-1589-08 chr1:44442959 G>A did not map to a codon.
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 chr3:64004273 C>A did not map to a codon.
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 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 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 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 chr2:97216936 G>A maps to NM_212481.1 G224G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:183551347 T>G maps to NM_018622.5 T320T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr3:183551347 T>G maps to NM_018622.5 T320T. Only missense variants will be evaluated by CHASM.
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 chr2:49190327 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 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 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 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 chr5:38954923 A>C maps to ENST00000296782 Y883*. Only missense variants will be evaluated by CHASM.
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 chr2:44508524 G>C did not map to a codon.
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 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 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 chr11:76867020 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 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 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 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 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 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 chr9:97063237 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 chr12:97137639 A>T maps to ENST00000342887 T928T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr12:97137639 A>T maps to ENST00000342887 T928T. 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 chr1:171605340 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 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 chr3:138456587 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 chrX:123519704 G>T maps to NM_001163278.1 T1966T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chrX:123519704 G>T maps to NM_001163278.1 T1966T. 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 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 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 chr3:49362338 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 chr9:124074614 A>T did not map to a codon.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr9:124074614 A>T did not map to a codon.
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 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 chr11:5717509 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 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 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 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 chr1:152279671 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 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 chr3:196214404 G>T maps to NM_152617.3 A141A. 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 chr2:212295692 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 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 chr11:4929157 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 chr14:21821860 C>T did not map to a codon.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr14:21821860 C>T did not map to a codon.
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.
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 chr5:73161822 C>T maps to NM_001080479.2 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr5:73161822 C>T maps to NM_001080479.2 Q713*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr8:109462687 A>T maps to NM_014673.3 A62A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr8:109462687 A>T maps to NM_014673.3 A62A. 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 chr9:131755474 G>A did not map to a codon.
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 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 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 chr10:858886 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 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 chr14:61434985 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 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 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 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 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 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 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 chr11:66627367 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 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 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 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 chr2:239988462 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 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 chr20:32376705 G>T maps to ENST00000375200 A630A. Only missense variants will be evaluated by CHASM.
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 chr14:51219340 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 chr19:52659396 G>A maps to NM_001102657.1 L513L. 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.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr10:71899793 G>A maps to NM_173555.2 Y529Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5903-01A-11D-1589-08 chr10:71899793 G>A maps to NM_173555.2 Y529Y. 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 chr2:96789882 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 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 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 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 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 chrX:48682179 G>A maps to ENST00000444343 R1110R. Only missense variants will be evaluated by CHASM.
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-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 chr2:180810242 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 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 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 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 chr9:36170074 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 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 chr6:83862019 T>A maps to NM_015018.2 P2021P. 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 chr12:29485565 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 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 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 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 chr17:78355390 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 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 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 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 chr9:21971119 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 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 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 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 chr1:115218254 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 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 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 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 chr6:35051231 C>A maps to NM_015245.2 I982I. 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 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 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 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 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 chr20:34778269 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 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 chr19:5914494 G>T maps to ENST00000394521 L159L. 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 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 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 chr3:127379598 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 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 chr1:13183398 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 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 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 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 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 chr9:86585224 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 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 chr17:37368583 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 chr4:48578145 T>C maps to NM_015030.1 A874A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6790-01A-11D-1961-08 chr4:48578145 T>C maps to NM_015030.1 A874A. 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 chr17:10227378 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 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 chr2:179419673 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 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 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 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 chr2:171687569 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 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 chr8:121237424 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 chrX:152937463 A>T maps to NM_001039582.3 G178G. 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-G7-6790-01A-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 chr2:185801067 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 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 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 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 chr6:26021007 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 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 chr5:138266341 C>T maps to ENST00000355078 R731*. 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 chr9:17332673 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 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 chr7:45747950 T>C maps to NM_021116.2 A940A. 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 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 chr17:37817258 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 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 chr12:75895545 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 chr1:11771906 G>A did not map to a codon.
Sequencing variant TCGA-G7-6792-01A-21D-1961-08 chr1:11771906 G>A did not map to a codon.
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 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 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 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 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 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 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 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 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 chr1:155912174 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 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 chr20:3016488 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 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 chr1:205132070 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 chr1:226075313 G>A maps to ENST00000419724 L283L. 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 chr17:76133426 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 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 chr4:159825695 A>G maps to ENST00000379346 *1138*. 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 chr12:109692083 C>T maps to NM_001093.3 L2037L. 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 chr2:179425265 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 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 chr10:15688932 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 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 chr11:66191470 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 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 chr21:17138431 C>G maps to ENST00000285681 Y80*. 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 chr16:20376784 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 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: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 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 chr10:16916467 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 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 chr1:157667659 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 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 chr11:108380879 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 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 chr10:99327794 G>A maps to NM_024954.3 K65K. 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 chr12:57918526 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 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 chr19:24310236 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 chr19:2408352 G>A did not map to a codon.
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 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 chr12:56118169 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 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 chr19:57037031 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 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 chr11:108032023 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 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 chr20:20491912 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 chr4:17586651 A>G maps to NM_015907.2 A199A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr4:17586651 A>G maps to NM_015907.2 A199A. 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 chr8:107718928 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 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 chr19:38774303 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 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 chr7:48506567 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 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 chr1:155630356 G>A maps to ENST00000368339 L586L. 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 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 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 chr1:98058808 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 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 chr4:8230106 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 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 chr7:122765635 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 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 chr15:44951364 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 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 chr19:41712374 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 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 chr17:8416921 C>T maps to ENST00000360416 L893L. Only missense variants will be evaluated by CHASM.
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 chr2:21260847 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 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 chr4:169317121 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 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 chr5:37381725 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 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 chr11:10647665 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 chr5:141524142 C>A maps to NM_030571.3 L190L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6795-01A-11D-1961-08 chr5:141524142 C>A maps to NM_030571.3 L190L. Only missense variants will be evaluated by CHASM.
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 chr3:39431017 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 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 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 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 chr6:43042367 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 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 chr1:157559027 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 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 chr19:36128156 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 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 chr13:48833063 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 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 chr1:6246872 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 chr1:39798097 A>T maps to ENST00000289893 L386L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr1:39798097 A>T maps to ENST00000289893 L386L. 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 chr12:21962861 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 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 chr17:45668144 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 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 chr1:10352149 A>G maps to ENST00000377086 G520G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:117655855 G>T maps to ENST00000338101 T1462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr12:117655855 G>T maps to ENST00000338101 T1462T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr7:66410207 T>C maps to NM_017994.4 H135H. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6796-01A-11D-1961-08 chr7:66410207 T>C maps to NM_017994.4 H135H. 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 chr2:219222363 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 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 chr5:140772926 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 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 chr16:67910483 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 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 chr11:61730353 C>T maps to NM_001139443.1 A516A. Only missense variants will be evaluated by CHASM.
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 chr13:39422802 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 chr22:30051665 G>A did not map to a codon.
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 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 chr8:37729418 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 chr3:48668740 T>C did not map to a codon.
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 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 chr19:50097990 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 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 chr8:24209519 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 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 chr3:50379016 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 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 chr16:2511751 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 chr16:89717998 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 chr16:89717998 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 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 chr2:17955657 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 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 chr3:58517531 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 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 chr8:141745381 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 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 chr11:49974075 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 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 chr8:56435873 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 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 chr15:38988924 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 chr19:38230138 C>A maps to NM_001172690.1 E418*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-6797-01A-11D-1961-08 chr19:38230138 C>A maps to NM_001172690.1 E418*. 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:117731502 A>T maps to ENST00000276204 A791A. 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 chr13:33095587 T>C did not map to a codon.
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 chr3:120122158 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 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 chr2:26532907 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 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 chr1:33960784 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 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 chr2:231741582 G>C maps to NM_030926.4 A154A. 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 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 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 chr6:39159333 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 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 chr1:207105816 C>G maps to NM_002644.3 R664R. Only missense variants will be evaluated by CHASM.
Alternatively spliced codon TCGA-G7-7501-01A-11D-2201-08. Mapping will be selected arbitrarily.
Alternatively spliced codon TCGA-G7-7501-01A-11D-2201-08. Mapping will be selected arbitrarily.
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 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 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 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 chr7:120629776 C>G maps to NM_024913.4 T34T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7501-01A-11D-2201-08 chr7:120629776 C>G maps to NM_024913.4 T34T. 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 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 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 chr1:207085118 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 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 chr4:89575197 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 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 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 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 chr1:153736637 A>G maps to ENST00000428986 L623L. 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 chr3:108110609 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 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 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 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 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 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 chr20:5903929 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 chr7:27211694 C>T maps to NM_018951.3 E352E. 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-G7-7502-01A-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 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 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 chr1:28477259 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 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 chr6:32945265 T>C maps to ENST00000395289 A416A. 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 chr2:175215407 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 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 chr3:122128620 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 chr16:50104087 G>A did not map to a codon.
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 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 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 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 chr6:139563746 T>C maps to ENST00000358430 A657A. Only missense variants will be evaluated by CHASM.
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 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 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 chr1:7845602 A>C maps to ENST00000377532 L77L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:196762615 G>T maps to NM_021023.5 G322G. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr1:196762615 G>T maps to NM_021023.5 G322G. 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 chr2:219556969 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 chr22:37334444 G>T maps to ENST00000262825 V871V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr22:37334444 G>T maps to ENST00000262825 V871V. 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 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 chr3:52022537 A>C did not map to a codon.
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 chr15:79059039 A>G maps to ENST00000258883 N1071N. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-G7-7502-01A-11D-2201-08 chr15:79059039 A>G maps to ENST00000258883 N1071N. Only missense variants will be evaluated by CHASM.
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 chr3:52554290 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 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 chr17:46058012 C>T maps to NM_176096.1 L378L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr9:135917679 T>A maps to NM_001122823.1 I120I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr9:135917679 T>A maps to NM_001122823.1 I120I. 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 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 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 chr8:61654761 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 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 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 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 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 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 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 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 chr14:44975260 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 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 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 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 chr11:6048448 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 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 chr20:47641989 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 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 chr7:107808821 G>A maps to ENST00000379032 S1071S. 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 chr17:5009511 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 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 chr4:106157460 G>T maps to ENST00000513237 E809*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:26684350 C>T maps to NM_015584.3 Q41Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr17:26684350 C>T maps to NM_015584.3 Q41Q. 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 chr3:195006525 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 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 chr19:41306602 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 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 chr4:122853524 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 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 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 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 chr2:219503379 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 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 chr3:169706124 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 chr12:22623803 C>T maps to ENST00000446597 Q800Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chr12:22623803 C>T maps to ENST00000446597 Q800Q. 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 chr17:73831765 G>T maps to ENST00000412096 L563L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chrX:53111964 C>G maps to NM_022117.3 P95P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-6846-01A-11D-1961-08 chrX:53111964 C>G maps to NM_022117.3 P95P. 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-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-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 chr7:95818644 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 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 chr11:63885634 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 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 chr9:92007356 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 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 chr10:16941135 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 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 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 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 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 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 chr3:48266892 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 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 chr2:182543428 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 chr17:1375217 G>A maps to NM_001080779.1 Y668Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr17:1375217 G>A maps to NM_001080779.1 Y668Y. 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 chr2:179599139 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 chr1:43828620 G>A did not map to a codon.
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 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 chr3:38316609 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 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 chr12:11420474 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 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 chr14:65008124 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 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 chr19:35250174 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 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 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 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 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 chr17:65134124 G>A maps to NM_014877.3 Q959*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr17:65134124 G>A maps to NM_014877.3 Q959*. Only missense variants will be evaluated by CHASM.
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: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 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 chr1:111862961 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 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 chr3:98309566 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 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 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 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 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 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 chr2:97428004 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 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 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 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 chr11:58978385 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 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 chr3:62317064 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 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 chr2:197889958 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 chrX:46401550 T>A did not map to a codon.
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 chr12:10541381 G>A maps to NM_007360.3 R10*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-7773-01A-11D-2136-08 chr12:10541381 G>A maps to NM_007360.3 R10*. 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 chr9:102730747 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 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 chr14:24709983 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 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 chr15:51790749 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 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 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 chr12:29469909 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 chr12:29469909 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 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 chr6:71003974 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 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 chr12:40758850 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 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 chr1:192128418 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 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 chr14:101012902 G>A maps to NM_020836.3 H37H. 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 chr17:6531559 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 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 chr15:25207296 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 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 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 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 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 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 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 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 chr2:166201261 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 chr2:168105758 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 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 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 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 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 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 chr2:179598481 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 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 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 chr1:155451418 T>C maps to ENST00000368346 A414A. 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 chr15:70987422 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 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 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 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 chr2:88890365 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 chrX:152823736 C>T maps to NM_001001344.2 A867A. 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-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 chr1:158517502 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 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 chr5:9629373 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 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 chr7:142561392 A>T maps to NM_004445.3 V35V. 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 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 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 chr8:95262645 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 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 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 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 chr19:39058442 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 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 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 chr9:125751641 C>T maps to NM_012197.3 V219V. 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-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 chr9:35869822 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 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 chr19:13346024 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 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 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 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 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 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 chr3:38404483 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 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 chr19:2290212 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 chr19:45868314 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 chr19:45868314 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 chr12:124887098 T>C maps to NM_006312.4 Q497Q. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-GL-8500-01A-11D-2396-08 chr12:124887098 T>C maps to NM_006312.4 Q497Q. 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 chr19:7075687 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 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 chr18:48331526 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 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 chr16:23848698 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 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 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 chr3:178785386 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 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 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 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 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 chr20:2776795 C>G maps to NM_019609.4 L418L. 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 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 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 chr6:43112986 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 chr9:131394991 G>A maps to NM_001130438.2 P2385P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr9:131394991 G>A maps to NM_001130438.2 P2385P. 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 chr9:4706078 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 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 chr8:41467378 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 chr20:17950810 C>A maps to NM_052865.2 I103I. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7128-01A-11D-1961-08 chr20:17950810 C>A maps to NM_052865.2 I103I. 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 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 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 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 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 chr7:99621200 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 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 chr17:16285475 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 chr17:61511912 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 chr17:61511912 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 chr17:60501295 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 chr17:60501295 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 chr17:38182476 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 chr17:38182476 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 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 chr10:75898089 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 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 chr1:156818723 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 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 chr11:57076185 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 chr3:56330163 G>T maps to ENST00000460849 S319S. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7129-01A-11D-1961-08 chr3:56330163 G>T maps to ENST00000460849 S319S. 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 chr20:19955385 C>T maps to ENST00000255006 S288S. 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 chr7:45112358 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 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 chr14:35242929 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 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 chr17:79913364 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 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 chr3:134323199 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 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 chr13:113964010 C>T maps to NM_005561.3 S79S. 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 chr6:43008725 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 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 chr5:82786053 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 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 chr17:39887799 G>A maps to ENST00000310778 L338L. 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 chr1:154544110 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 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 chr2:63826355 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 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 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 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 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 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 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 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 chr12:66522753 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 chr4:155505887 G>A maps to NM_000508.3 C663C. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr4:155505887 G>A maps to NM_000508.3 C663C. 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 chr7:150720229 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 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 chr11:117097975 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 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 chr14:24775202 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 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 chr7:143175819 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 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 chr5:71495627 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 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 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 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 chr11:4936272 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 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 chr5:140856909 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 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: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 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 chr5:156186310 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 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 chr2:32626578 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 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 chr1:44063521 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 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 chr13:52603704 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 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 chr8:99019719 C>T maps to ENST00000254898 C488C. Only missense variants will be evaluated by CHASM.
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 chr11:68197136 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 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 chr17:46239836 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 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 chr9:123783918 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 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 chr10:45472881 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 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: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 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 chr18:22048830 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 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 chr17:78120724 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 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 chr19:55450842 G>A maps to ENST00000446217 F476F. 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 chr12:121648005 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 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 chr1:158735809 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 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 chr19:51518765 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 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 chr16:56518731 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 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 chr12:118293233 T>C maps to ENST00000339824 S157S. 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 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 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 chr10:61830688 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 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 chr1:21226357 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 chr1:11775242 C>T maps to NM_198545.3 F305F. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:11775242 C>T maps to NM_198545.3 F305F. 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 chr1:44063473 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 chr1:22413328 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 chr1:22413328 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 chr1:155723184 G>A maps to ENST00000368331 Y1884Y. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chr1:155723184 G>A maps to ENST00000368331 Y1884Y. 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 chr10:61830132 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 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 chr1:22413229 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 chr1:158576302 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 chr1:158576302 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 chr1:2341813 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 chr1:2341813 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 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 chr22:21140327 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 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 chr1:180044160 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 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 chr6:31324627 G>A maps to ENST00000428231 F60F. 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 chr22:26702083 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 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 chr1:38338747 G>A maps to ENST00000373026 L761L. Only missense variants will be evaluated by CHASM.
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 chr10:72360283 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 chrX:44870204 G>C did not map to a codon.
Sequencing variant TCGA-HE-7130-01A-11D-1961-08 chrX:44870204 G>C did not map to a codon.
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 chr2:149248039 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 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 chr12:112668607 G>A maps to NM_001109662.2 P1901P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr12:112668607 G>A maps to NM_001109662.2 P1901P. 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 chr19:42814765 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 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 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 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 chr4:3519767 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 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 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 chr10:103563516 A>G maps to NM_012215.3 N337N. 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.
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 chr5:80040401 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 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 chr15:35085734 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 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 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 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 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 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 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 chr11:76903187 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 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 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 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 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 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 chr5:177580731 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 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 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 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 chr2:85875074 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 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 chr1:15987647 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 chr15:90118912 C>A maps to NM_152259.3 T32T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr15:90118912 C>A maps to NM_152259.3 T32T. 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 chr2:54080606 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 chr9:139273026 C>G maps to NM_003086.2 G1084G. 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-8195-01A-31D-2396-08 chr5:17275783 G>A maps to NM_006317.3 A153A. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8195-01A-31D-2396-08 chr5:17275783 G>A maps to NM_006317.3 A153A. 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 chr19:2255342 G>A did not map to a codon.
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 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 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 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 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 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 chr1:152748939 A>T maps to ENST00000439693 P31P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:152748939 A>T maps to ENST00000439693 P31P. 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 chr16:61851549 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 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 chr1:15956838 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 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 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 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 chr17:12016634 T>C maps to ENST00000415385 S268S. 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 chr8:94747483 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 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 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 chr3:48956090 T>A maps to NM_001123040.1 P164P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr3:48956090 T>A maps to NM_001123040.1 P164P. 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 chr5:140223200 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 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 chr1:110882977 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 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 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 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 chr4:46312217 A>T maps to ENST00000507069 A177A. 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 chr2:11960559 A>G maps to ENST00000396099 V853V. 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 chr17:40695934 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 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 chr5:122359695 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 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 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 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 chr17:42117588 C>T maps to ENST00000411445 K101K. 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 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 chr6:30640453 G>T maps to NM_003587.4 L55L. 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 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 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 chr5:130500844 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 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 chr21:47542787 G>A did not map to a codon.
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 chr1:156309582 G>C did not map to a codon.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr1:156309582 G>C did not map to a codon.
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 chr14:23549775 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 chr8:143956728 C>G did not map to a codon.
Sequencing variant TCGA-J7-6720-01A-11D-2136-08 chr8:143956728 C>G did not map to a codon.
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 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 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 chr14:24793366 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 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 chr8:75227664 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 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 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 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 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 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 chr16:74640707 A>C maps to NM_012201.5 G95G. 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 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 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 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 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 chr10:17495607 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 chr14:105349546 T>C maps to ENST00000453495 D252D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-J7-8537-01A-11D-2396-08 chr14:105349546 T>C maps to ENST00000453495 D252D. 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 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 chrX:144904237 C>T maps to NM_001144010.2 Q99*. 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-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 chr17:38187789 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 chr1:3334450 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 chr1:94009755 G>A maps to ENST00000370253 Q414Q. 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 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 chr16:19051690 C>A maps to NM_024847.3 I420I. 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 chr2:86371414 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 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 chr10:105793763 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 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 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 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 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 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 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 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 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 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 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 chr2:233681743 T>A did not map to a codon.
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 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 chr2:48050457 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 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 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 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 chr4:138450854 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 chr17:40725219 C>G did not map to a codon.
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 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 chr15:40594159 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 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 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 chr11:63129876 C>T did not map to a codon.
Sequencing variant TCGA-B3-3925-01A-01D-1458-08 chr11:63129876 C>T did not map to a codon.
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: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 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 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 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 chr18:44662720 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 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 chr10:129859260 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 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 chr15:72192124 T>G maps to ENST00000424560 R1125R. 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 chr4:146041305 G>A did not map to a codon.
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-B3-3925-01A-01D-1458-08 chrX:16685794 A>C maps to NM_001144002.1 L414L. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3925-01A-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 chr2:215440517 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 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 chr4:76532404 T>C maps to ENST00000307465 R168R. Only missense variants will be evaluated by CHASM.
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 chr22:24447424 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 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 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 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 chr22:32193640 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 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 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 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 chr4:90035226 G>T maps to NM_145715.2 E368*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr17:16701803 C>T did not map to a codon.
Sequencing variant TCGA-B3-3926-01A-01D-1252-08 chr17:16701803 C>T did not map to a codon.
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 chr22:24581139 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 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 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 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 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 chr3:196387839 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 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 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 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 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 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 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 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 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 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 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 chr19:10230529 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 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 chr4:56301653 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 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 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 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 chr7:117364733 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 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 chr3:195974372 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 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 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 chr3:124515612 C>A maps to NM_002213.3 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:124515612 C>A maps to NM_002213.3 E439*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:124515613 C>T maps to NM_002213.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4103-01A-01D-1458-08 chr3:124515613 C>T maps to NM_002213.3 T438T. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B3-4104-01A-01D-1252-08 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-1252-08 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 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 chr3:19925988 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 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 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 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 chr1:1334455 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 chr12:49426525 G>A maps to NM_003482.3 Q3988*. 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-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 chr22:44564536 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 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 chr14:45603574 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 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 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 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 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 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 chr1:113126669 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 chr15:51857283 C>A did not map to a codon.
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 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 chr14:36005047 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 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 chr2:152397246 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 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 chr6:32947798 C>G maps to ENST00000395289 S714*. 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 chr1:154493834 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 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 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 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 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 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 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 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 chr19:757668 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 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 chr14:69256348 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 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 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 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 chr2:67631298 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 chrX:123176468 C>T maps to NM_001042750.1 R146*. 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-B3-4104-01A-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 chr1:12854435 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 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 chr17:7579414 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 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 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 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 chr17:42828062 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 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 chr9:34397496 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 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 chr15:26793189 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 chr3:9547648 G>A did not map to a codon.
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 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 chr2:100623249 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 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 chr6:32945958 C>G maps to ENST00000395289 P545P. 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 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 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 chr1:148025785 G>A maps to ENST00000310701 Q21*. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr7:102040095 G>A did not map to a codon.
Sequencing variant TCGA-B9-4113-01A-01D-1252-08 chr7:102040095 G>A did not map to a codon.
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 chr2:186671399 T>C maps to NM_173651.2 D5878D. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr17:16701680 C>A did not map to a codon.
Sequencing variant TCGA-BQ-7061-01A-11D-1961-08 chr17:16701680 C>A did not map to a codon.
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 chr17:4837737 A>G maps to NM_000173.5 V613V. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr9:17010 T>C maps to NM_182905.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-EV-5902-01A-11D-1589-08 chr9:17010 T>C maps to NM_182905.4 P279P. Only missense variants will be evaluated by CHASM.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:149398785 C>T did not map to a codon.
Sequencing variant TCGA-IZ-8196-01A-11D-2396-08 chr1:149398785 C>T did not map to a codon.
